Lediga jobb Oticon Medical AB i Göteborg

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PhD or Post PhD Implant Researcher

Join us in making a difference by developing novel concepts and implant systems for next-generation bone-conduction hearing solutions. Are you a PhD or Post PhD passionate for technology and advances on science? Do you want to improve the life experience for people with a hearing disability? Do you also have a strong experience with implant development and analysis? Then we might have an exciting career for you as Translational Research Manager at the Re... Visa mer
Join us in making a difference by developing novel concepts and implant systems for next-generation bone-conduction hearing solutions.
Are you a PhD or Post PhD passionate for technology and advances on science? Do you want to improve the life experience for people with a hearing disability? Do you also have a strong experience with implant development and analysis?
Then we might have an exciting career for you as Translational Research Manager at the Research & Technology Department at Oticon Medical in Gothenburg.
Our product
Oticon Medical is committed to improve the quality of life of people with hearing disabilities. For that, we develop implantable medical devices and surgical techniques for Bone Anchored Hearing Systems (BAHS) to restore hearing loss. We are a fast growing and agile company, ambitious and possess an entrepreneur spirit and the will to win. Here, we offer an opportunity to join us on our exciting journey and to help us develop innovative implantable hearing solutions that improve the lives of children and adults across the globe.
Solid experience with active implantable devices
You will be joining Oticon Medical’s Research & Technology (R&T) team in Gothenburg (Sweden) where you will work with the development of our next generation bone-conduction implant systems and initiate and manage research project internally and together with external partners. We are a dynamic, ambitious, international, curiosity-driven crew of engineers and scientists dedicated to shaping the future of hearing implant solutions. We investigate, conceptualise, prototype, implement, communicate, and share our vision and our work with Oticon Medical’s product development and clinical teams. We work closely with our academic and external clinical partners across the globe and share with them our passion to make a difference for patients and professionals in the field.
Your core responsibility will be to lead and manage translational research project aligned to our long term roadmap for next generation of bone-anchored hearing devices. Your key responsibilities include:
• Assuring development of prototypes, concept demonstrations and publications.
• Work towards impact on products and strategy
• Conceptualise, design, prototype, and test implant design and solutions
• Lead technology & research projects
• Perform scouting & technology evaluations
• Promote Oticon Medical as a scientific partner to current and new academic, technology and clinical partners
• Development of Prototypes and Proof of Concept for technologies
• Execute technology evaluations (maturity, make/buy assessments, commercial relevance for technology transfer scoping)
• Evaluate and generate project proposals for internal & external research or technology collaborations, incl. grant/funding application
• Advance concept projects by demonstrating expertise, creativity, and engineering leadership in mechanical design and biomaterial science
• Lead cross-functional teams
• Influences the roadmap by proposing new solutions that support the strategic agenda
• Supervise or oversee consultants or students working on the projects you are accountable for
Successful on the job
For you to be successful in this job, we are looking on following skills and qualifications:
• PhD in mechanical, biomechanical, biomaterials, or biomedical engineering, or similar
• Experience in new product development of implantable medical devices is required. Experience with active implantable medical devices is a plus.
• Track record of successful endeavours in concept development of implantable devices and systems. Experience in translation of medical device research and concepts into product development and clinic is a plus
• Strong knowledge in methods for implant and biomaterials evaluation
• Strong skills as an innovator and problem solver
• Experience of working on multi-disciplinary teams, with exposure to systems, electrical, and mechanical engineering
• Fluency in English (both spoken and written).
How to become part of us?
We are screening applications continuously and would like to receive your application not later than October 2025
If you wish to know more about the position, feel free to contact Martin Johansson, [email protected].
We look forward to hearing from you.
Öppen för alla
Vi fokuserar på din kompetens, inte dina övriga förutsättningar. Vi är öppna för att anpassa rollen eller arbetsplatsen efter dina behov. Visa mindre

Controller till Medtech företag

Ansök    Jan 23    Oticon Medical AB    Controller
Welcome to Oticon Medical We are a MedTech company located in Askim, Gothenburg. Our owner is the listed company Demant in Denmark where Group HQ is located. Group HQ includes 45 great financial colleagues, consisting of Financial- & Business Controlling, FP&A, Tax, Treasury and Finance Systems & Processes. Those tasks that are related to the Swedish company are going to be moved to Sweden step by step since the aim is to be a stand-alone company going for... Visa mer
Welcome to Oticon Medical
We are a MedTech company located in Askim, Gothenburg. Our owner is the listed company Demant in Denmark where Group HQ is located. Group HQ includes 45 great financial colleagues, consisting of Financial- & Business Controlling, FP&A, Tax, Treasury and Finance Systems & Processes. Those tasks that are related to the Swedish company are going to be moved to Sweden step by step since the aim is to be a stand-alone company going forward.

This is us – the team
Our biggest value is our team spirit, as we believe that the best results come from a fruitful collaboration. Our environment is based on trust and openness. We offer flexible working conditions and work life balance is important to us. Our working culture is characterized by respect and kindness.
You will be joining the Finance team in Sweden where we are responsible for preparing and controlling the internal and external financial reporting of the Swedish Company as well as the consolidation reporting for the Business Area.
We are building a team here of central functions at the HQ for Oticon Medical which this role will be one of the upcoming positions within finance. At the office in Askim, we have around 60 employees covering R&D, marketing, operations, RA/QA and product/project management.

What are we looking for in this specific role?
You will be working with accounting, reporting and controlling for the Swedish entity and also helping to implement, integrate systems and routines together with the Finance manager.
We have a close communication and proactive engagement with the shared service center in Poland, ensuring high quality insights into the financials and analysis on internal and external reporting. You will ensure a solid foundation for business decisions by translating the financials into accurate and timely reporting and insight to management.
Having a talent for “working smarter” you will be part of driving improvements in the Financial Accounting & Controlling process across functions, countries and organizational layers and develop smart solutions leveraging available IT tools together with finance manager.
Responsibilities will include among others:
Participate in and ensure strong monthly/quarterly/yearly financial controlling and reporting for your areas of responsibility.
Responsible for monthly input and reconciliation in collaboration with shared service center in Poland for the Swedish entity.
Participate in preparing the annual reports and assist the auditors in the audit process for the Swedish legal entity.
Taking part in yearly budget process.
Participate in defining and drive projects from end to end with the purpose of continually improving reporting and ensuring compliance.
Ensure compliance with IFRS and accountant standards.


Who are you? Are we a perfect match?
Ideally, you have a master’s degree in business administration, Finance, Accounting or equivalent, combined with a few years of experience from an international company. We also value self-willingness and drive to learn and to find information.
You are a dedicated and business-oriented person by nature with a good sense of quality and humor. You enjoy collaborating with colleagues from various functions and organizational levels. You are a structured and analytical person. You act with integrity, simplicity, and accountability in your work, and you appreciate working in an international environment with highly competent colleagues.
Qualifications likely required to be successful
You have experience with consolidation principles, controlling, and reporting processes, plus understanding of the audit process.
You are a pro-active user of IT/accounting systems and have hands-on experience with financial ERP systems and BPC systems.
Your mindset is data-driven with strong analytical and numerical skills and interest in automation and improvements of processes and reporting.
You can make complex task simple - in respect of processes, tools, and communication.
You have good communication skills in both verbal and written English.
Preferably you have good knowledge in VAT.


Do you want to join the team?
We are looking forward to hearing from you. Kindly submit your application as soon as possible, as we are screening applications on a continuous basis. Visa mindre

Regulatory Affairs Manager, Market Authorization

Fråga en anställd på Oticon Medical vad den mest givande aspekten av deras arbete är, de flesta skulle utan att tveka säga "Att göra skillnad". Det är det som får oss att gå upp på morgonen – att utveckla avancerade, benförankrade hörsellösningar. Vi tror att leendet på treåringens läppar när han eller hon hör föräldrarnas röst för första gången är värt alla våra ansträngningar! Vår bakgrundshistoria Oticon Medical har åtagit sig att förbättra livskvalitet... Visa mer
Fråga en anställd på Oticon Medical vad den mest givande aspekten av deras arbete är, de flesta skulle utan att tveka säga "Att göra skillnad". Det är det som får oss att gå upp på morgonen – att utveckla avancerade, benförankrade hörsellösningar. Vi tror att leendet på treåringens läppar när han eller hon hör föräldrarnas röst för första gången är värt alla våra ansträngningar!
Vår bakgrundshistoria
Oticon Medical har åtagit sig att förbättra livskvaliteten för patienter med hörselnesättning. Vi utvecklar implanterbara medicinska produkter som hjälper människor med hörselnedsättning att höra igen eller höra för allra första gången
Som medlem i Demant Group, en av världens största koncerner inom hörselvård, delar vi en nära koppling med Oticon och direkt tillgång till de senaste framstegen inom hörselforskning och teknik. Vår kompetens sträcker sig över mer än ett sekel av innovationer inom ljudbehandling och decennier av banbrytande erfarenhet inom hörselimplantats-teknik. Med en idag stark produktportfölj och global närvaro ser vi in ??i en intressant framtid med utveckling av fler produkter och ännu fler patienter att hjälpa.
Vår resa har börjat – vill du vara med?
Vi är ett team om tre i Göteborg som ansvarar för att säkerställa följsamhet av våra produkter världen över. Det är vår uppgift att fastställa regulatoriska strategier, säkerställa upprättandet och underhållet av tekniska filer, och vägleda utvecklingsprojekt för att uppfylla kvalitetsledningssystemet. Vår produktportfölj sträcker sig från medicinsk utrustning i klass I till klass III, elektronisk utrustning med både inbyggd och fristående programvara, icke-aktiva och aktiva implantat, kirurgiska instrument och tillbehör.
För att beskriva vårt team på bästa sätt tror vi på en samarbetsvillig, stödjande och öppen kultur. Vi är beroende av varandra för att dela kunskap och utmaningar eftersom vi tror att de bästa resultaten kommer från en tvärfunktionell laginsats. Vi arbetar tvärvetenskapligt med våra kollegor i Göteborg, hos leverantörer och våra distributörer världen över.
Kollegan vi söker nu kommer att hantera våra globala marknadsregisteringar och även vara en del av produktutvecklingsprojekt.Tjänsten är på heltid med möjlighet att arbeta hemifrån två dagar i veckan (om så önskas). Du kan förvänta dig 5-10 dagars resa årligen.
Ansvar i korthet
Ditt ansvar är att säkerställa homologering/marknadsgodkännanden och frisläppande av produkter. Som start kommer du vara nyckelperson i att planera och lansera vårt helt nya klass III benförankrade hörselsystem välden över. Du:
o deltar i att skapa regulatoriska strategier och ger regulatorisk input till produktlanseringsplaner
o förbereder regulatorisk dokumentation för produktregistreringar, licensförnyelser och periodiska uppdateringar, antingen direkt eller i samarbete med våra lokala distributörer
o identifierar krav, säkerställer efterlevnad av regler och driver förbättringar
o samordnar aktiviteter relaterade till uppstarten av ett nytt land
o genomför revisioner av distributörers kvalitetsledningssystem och säkerställer uppföljning och stängning av CAPA
o genomför utbildning av distributörer i QARA aspekter och säkerställer kommunikation av uppdaterade dokument
Som en del av ditt arbete kan du också förvänta dig att inkluderas i produktutvecklingsprojekt, vilket hjälper nya produkter att gå från de tidiga stadierna till faktiska produkter som hjälper människor att höra.
Vem vi letar efter
Vi söker en positiv, talangfull person med integritet och hjärtat på rätt plats. Du brinner för effektivitet, struktur och samarbete. Du är pragmatisk och förstår utmaningarna med att arbeta i en snabbt växande mångkulturell miljö.
För att prestera bra i denna roll behöver du:
• Gärna minst 2 års arbetslivserfarenhet inom QA/RA
• Förståelse för globala regler för medicintekniska produkter, ISO 13485 och MDSAP
• Vara lyhörd, kommunikativ och van att arbeta i ett team
• Serviceinriktad för att hjälpa kollegor runt om i världen att få våra produkter registrerade
• Planerings- och drivförmåga för att möjliggöra produktlanseringar enligt plan
Du tycker om att tolka och översätta mellan tekniska utmaningar, dokumentation och regulatoriska krav. Eftersom vi är ett globalt företag kommunicerar du enkelt både skriftligt och muntligt på engelska.
Vi ser fram emot att lära känna dig! Visa mindre

Transducer Developer

Are you ready to make a difference for people with a severe hearing disability? Our mission is clear: We want hearing impaired to be able to experience the sounds of life. This is the foundation for everything we do. This is what drives us and keeps us focussed on innovation and efficiency. We want to develop the world’s best hearing healthcare solutions. Nothing less. We are constantly moving the boundary for what is technically possible for sound quality... Visa mer
Are you ready to make a difference for people with a severe hearing disability?
Our mission is clear: We want hearing impaired to be able to experience the sounds of life. This is the foundation for everything we do. This is what drives us and keeps us focussed on innovation and efficiency. We want to develop the world’s best hearing healthcare solutions. Nothing less.
We are constantly moving the boundary for what is technically possible for sound quality, efficiency, and size. We are therefore looking for a Developer within Electrical Engineering to take up this challenge together with us.

Our products
Oticon Medical is committed to improve the quality of life of children and adults, with hearing disabilities, around the globe. For that, we develop implantable hearing solutions such as the Bone Anchored Hearing Systems (BAHS) here in Gothenburg. We are an agile and fast-growing company with an entrepreneurial spirit. Here, we offer an opportunity to join us on our exciting journey to develop innovative implantable hearing solutions. The core part of the complete, in-house developed hearing system for the BAHS is the vibrator with is based on electromagnetic or piezo electric transducers.

Successful in the job
As an R&D Developer in the Transducer System team, you will work with the development of our electromagnetic and piezo vibrators. You will be involved in the development of our next generation transducers for bone-conduction implant systems; from conceptualisation and prototyping to design, V&V and design transfer. When the product is launched, we ensure that products evolve and improve even after launch. You enjoy working over multiple technical areas like electromagnetics, piezoelectrics, physics, electronics, mechanics, and acoustics. In this job you have the chance to work with detailed transducer design while being an integral part of the BAHS product development team, giving context and the big picture to your work.
You are used to drive your tasks independently and take initiatives. We are a diverse team, and we believe combining our individual strengths makes us even stronger as a team, together. As we are a medical device company you see documentation as an asset for future development and a way to show the good work you have done.
For you to be successful in this job, we are looking for following skills and qualifications:
You are at the start of your career.
Min. a B.Sc., preferred a M.Sc. degree in Electromagnetics, Physics or Electronics
You have taken courses within electromagnetic design and/or transducers.
Comfortable with hands-on laboratory work
Strong in technical documentation
Fluent in English, both written and spoken


It is a merit if you have worked with one/multiple of the following:
Audio applications
FEM Simulation of electromagnetics (and piezo)
Piezoelectric materials and applications
Matlab
Ltspice



How to apply
Please send your application directly to Johannes Kocher, Head of Transducer System at [email protected].
Recruitment agency? Thank you for your interest, but we are sourcing all our candidates directly or via our preferred suppliers. We appreciate you trying but please keep in mind that any unsolicited profiles you send us will be treated as direct applications from the candidates.

About Oticon Medical:
Oticon Medical is a global company in implantable hearing solutions, dedicated to bringing the magical world of sound to people at every stage of life. By working collaboratively with patients, physicians and hearing care professionals, we ensure that every solution we create is designed with user needs in mind. We share an unwavering commitment to provide innovative solutions and support that enhance the quality of life for people wherever life may take them. Because we know how much sound matters. Visa mindre

Senior Implant Research Engineer

Ansök    Feb 18    Oticon Medical AB    Biomedicinare
Oticon Medical is committed to improve the quality of life of people with hearing disabilities. For that, we develop implantable medical devices and surgical techniques for Bone Anchored Hearing Systems (BAHS) and Cochlear Implants (CI) to restore hearing loss. We are a fast growing and agile company, ambitious and possess an entrepreneur spirit and the will to win. Here, we offer an opportunity to join us on our exciting journey and to help us develop inn... Visa mer
Oticon Medical is committed to improve the quality of life of people with hearing disabilities. For that, we develop implantable medical devices and surgical techniques for Bone Anchored Hearing Systems (BAHS) and Cochlear Implants (CI) to restore hearing loss. We are a fast growing and agile company, ambitious and possess an entrepreneur spirit and the will to win. Here, we offer an opportunity to join us on our exciting journey and to help us develop innovative implantable hearing solutions that improve the lives of children and adults across the globe.
Solid experience with active implantable devices
You will be joining Oticon Medical’s Research & Technology (R&T) team in Gothenburg (Sweden), Smørum (Denmark) or Nice (France) (based in availability) where you will work with the development of our next generation bone-conduction implant systems. We are a dynamic, ambitious, international, curiosity-driven crew of engineers and scientists dedicated to shaping the future of hearing implant solutions. We investigate, conceptualise, prototype, implement, communicate, and share our vision and our work with Oticon Medical’s product development and clinical teams. We work closely with our academic and external clinical partners across the globe and share with them our passion to make a difference for patients and professionals in the field.
Your core responsibility will be to conceptualise, prototype, test, and validate proof-of-concept implants for next generation of bone-anchored hearing devices. Your key responsibilities include:
• Conceptualise, design, prototype, and test implant design and solutions
• Advance concept projects by demonstrating expertise, creativity, and engineering leadership in mechanical design and biomaterial science
• Lead cross-functional teams to achieve project goals
• Influences the roadmap by proposing new solutions that support the strategic agenda
• Consult on mechanical-related concepts driven within the Research & Technology team
• Contribute to team efforts across departments for the projects you may not directly drive
• Supervise or oversee consultants or students working on the projects you are accountable for
Successful on the job
For you to be successful in this job, we are looking on following skills and qualifications:
• MSc or PhD in mechanical, biomechanical, or biomedical engineering, or similar
• At least 5 years’ experience in new product development of implantable medical devices is required. Experience with active implantable medical devices is a plus.
• Track record of successful endeavours in concept development of implantable devices and systems. Experience in translation of medical device research and concepts into product development and clinic is a plus
• Strong skills as an innovator and problem solver
• Proficient with mechanical design and simulation tools, and mechanical prototyping methods
• Motivated by hands-on mechanical concept development, design, and prototyping
• Experience of working on multi-disciplinary teams, with exposure to systems, electrical, and mechanical engineering
• Fluency in English (both spoken and written).
How to become part of us?
We are screening applications continuously and would like to receive your application not later than April
If you wish to know more about the position, feel free to contact Martin Johansson, [email protected].
We look forward to hearing from you.
About Oticon Medical
Oticon Medical is a global company in implantable hearing solutions, dedicated to bringing the magical world of sound to people at every stage of life. As part of the Demant group, a global leader in hearing healthcare with 15,000 people in over 130 countries, we have access to one of the world’s strongest research and development teams, the latest technological advances and insights into hearing care.
Our competencies span more than a century of innovations in sound processing and decades of pioneering experience in hearing implant technology. We work collaboratively with patients, physicians and hearing care professionals to ensure that every solution we create is designed with users’ needs in mind. We share an unwavering commitment to provide innovative solutions and support that enhance quality of life for people wherever life may take them. Visa mindre

Senior Product Developer - Medical Devices

Are you ready to make a difference for people with a severe hearing disability, and are you fueled by professional pride and curiosity? Are you skilled within the area of fine mechanics design and do you want to be part of developing new and innovative implantable hearing solutions? Then we can offer you an exciting opportunity as a Senior Product Developer at Oticon Medical. At Oticon Medical, we develop both Bone Anchored Hearing Systems (BAHS) and C... Visa mer
Are you ready to make a difference for people with a severe hearing disability, and are you fueled by professional pride and curiosity? Are you skilled within the area of fine mechanics design and do you want to be part of developing new and innovative implantable hearing solutions?

Then we can offer you an exciting opportunity as a Senior Product Developer at Oticon Medical.


At Oticon Medical, we develop both Bone Anchored Hearing Systems (BAHS) and Cochlear Implants (CI). We are a fast growing and agile company. We are ambitious and possess an entrepreneur spirit and the will to win. We offer an opportunity to join us on our exciting journey and to help us develop innovative implantable hearing solutions that improve the lives of thousands of children and adults across the globe.

About the job
As a Senior Product Developer, you will be based in Gothenburg and part of Oticon Medical BAHS R&D. Our project activities are however distributed across several sites (Gothenburg, Copenhagen, Nice and Stettin), so multi-site cooperation will be a natural part of your daily work.

Our project activities cover both development of new products and investigation and preparation of new technologies, and our project teams are typically multi-disciplinary and can include R&D, Operations, Regulatory, Clinical as well as Marketing. For our implant projects, the core development team will typically be located in Gothenburg.


Your focus will be to develop implants and accessories but also to act as specialist on all mechanical design with regards to manufacturability, robustness and best practice. You will work close with our research functions as well as our marketing department.

Successful in the job
For you to be successful in this job, we are looking on following skills and qualifications:

B.Sc. or an M.Sc. degree in mechanical engineering/material science
5-10 years’ experience working in hardware development projects
A strong detailed understanding of manufacturing processes in fine mechanics preferably within titanium or other types of metal
Experienced working with technical documentation and have solid experience in 2D and 3D design
Preferably experience working in a medical device company or other regulated industry
Fluent in English (spoken/written)
Some experience of collaborating and working with suppliers (in cooperation with our purchasers)
An ability to identify and communicate areas for new products and product improvements to management
Experience in osseointegrated implants would be considered an advantage


How to become part of us?
This recruitment is handled by our recruitment partner, Moveup Consulting AB. To apply, please send your CV and a cover letter to [email protected]


If you have questions regarding Oticon Medical or this open position, please contact Tom Bergqvist at +46 (0)733 87 27 22.


We are screening applications continuously. Please send your CV and Cover letter, to Tom, no later than 16 August.

We look forward to hearing from you.

Because sound matters


Oticon Medical is a global company in implantable hearing solutions, dedicated to bringing the magical world of sound to people at every stage of life. As part of the Demant group, a global leader in hearing healthcare with 15,000 people in over 130 countries, we have access to one of the world’s strongest research and development teams, the latest technological advances and insights into hearing care.


Our competencies span more than a century of innovations in sound processing and decades of pioneering experience in hearing implant technology. We work collaboratively with patients, physicians and hearing care professionals to ensure that every solution we create is designed with users’ needs in mind. We share an unwavering commitment to provide innovative solutions and support that enhance quality of life for people wherever life may take them.


Because we know how much sound matters.










Your focus will be to develop implants and accessories but also to act as specialist on all mechanical design with regards to manufacturability, robustness and best practice. You will work close with our research functions as well as our marketing department.
Successful in the job
For you to be successful in this job, we are looking on following skills and qualifications:
B.Sc. or an M.Sc. degree in mechanical engineering/material science
5-10 years’ experience working in hardware development projects
A strong detailed understanding of manufacturing processes in fine mechanics preferably within titanium or other types of metal
Experienced working with technical documentation and have solid experience in 2D and 3D design
Preferably experience working in a medical device company or other regulated industry
Fluent in English (spoken/written)
Some experience of collaborating and working with suppliers (in cooperation with our purchasers)
An ability to identify and communicate areas for new products and product improvements to management
Experience in osseointegrated implants would be considered an advantage


How to become part of us?
We are screening candidates continuously. Please send your application as soon as possible and no later than 16th of August.
If you have questions regarding the position, please contact Hanna Peters at [email protected].
We look forward to hearing from you.
Because sound matters
Oticon Medical is a global company in implantable hearing solutions, dedicated to bringing the magical world of sound to people at every stage of life. As part of the Demant group, a global leader in hearing healthcare with 15,000 people in over 130 countries, we have access to one of the world’s strongest research and development teams, the latest technological advances and insights into hearing care.
Our competencies span more than a century of innovations in sound processing and decades of pioneering experience in hearing implant technology. We work collaboratively with patients, physicians and hearing care professionals to ensure that every solution we create is designed with users’ needs in mind. We share an unwavering commitment to provide innovative solutions and support that enhance quality of life for people wherever life may take them. Visa mindre

Research Technician

Are you ready to make a difference for people with a severe hearing disability, and are you fueled by professional pride and curiosity? Are you skilled within the area of fine mechanics manufacturing and do you want to be part of developing new and innovative implantable hearing solutions? Then we can offer you an exciting opportunity as Research Technician at Oticon Medical. We are a fast growing and agile company. We are ambitious and possess an entrepre... Visa mer
Are you ready to make a difference for people with a severe hearing disability, and are you fueled by professional pride and curiosity? Are you skilled within the area of fine mechanics manufacturing and do you want to be part of developing new and innovative implantable hearing solutions?
Then we can offer you an exciting opportunity as Research Technician at Oticon Medical. We are a fast growing and agile company. We are ambitious and possess an entrepreneur spirit and the will to win. We offer an opportunity to join us on our exciting journey and to help us develop innovative implantable hearing solutions that improve the lives of thousands of children and adults across the globe. This job relates to the BAHS products and the role is situated in modern offices in Askim, right outside Gothenburg.
We are seeking someone with typically an operator or operator group lead background that are technical curious and have good hands-on experience of fine-mechanics assembly. The role is an integral part of our R&D group based in Gothenburg, you will be a key player in an early phase of the project to build and evaluate prototypes as well as support testing within our maintenance work.


Successful in the job
For you to be successful in this job, we are looking on following skills and qualifications:
A few years of documented experience working in a manufacturing/laboratory environment, preferably with small mechanical part assembly. Experience of soldering, gluing, machining.
Skilled in use of computers and in using electrical and mechanical characterization equipment.
Proactive, not only reacting to situations but also anticipating future opportunities or problem, and act upon them in advance
Well structured and good documentation skills.
CAD experience is meriting
A proper work-life balance is a key focus area in our organization and while flexibility goes both ways you are able to travel up to 20 days per year.

Responsibilities include
Contribute to good electro and mechanical lab operation including safety and quality aspects by maintaining and managing the lab equipment.
Build prototypes of designs made in projects
Build fixtures in own tool shop
Measure and report on parts received from supplier
Link findings in prototyping to our global manufacturing network and our plant in Poland as well as the in-house developers.
Participate to the organization and planning of tasks
Document obtained results including writing of experimental reports in English



Would you like to know more?
If you would like to know more about the position, you are welcome to contact Head of R&D on [email protected].
To apply send your application and CV through our application website latest on 8th of August, 2021. Interviews will take place throughout.
We are looking forward to hearing from you. Visa mindre

Industrial PhD postion BAHS

Industrial PhD postion BAHS Sweden Research field: Biomaterials and bone conduction hearing implant Supervision: Anders Palmquist, PhD, Associated Professor, University of Gothenburg and Martin Johansson, PhD, MSc, Senior Translational Research manager, Oticon Medical. Scientific department: Research & Technology Department, Oticon Medical (PhD employment) and the Department of Biomaterials, Institute of Clinical Sciences at University of Gothenburg (aca... Visa mer
Industrial PhD postion BAHS
Sweden
Research field: Biomaterials and bone conduction hearing implant
Supervision: Anders Palmquist, PhD, Associated Professor, University of Gothenburg and Martin Johansson, PhD, MSc, Senior Translational Research manager, Oticon Medical.
Scientific department: Research & Technology Department, Oticon Medical (PhD employment) and the Department of Biomaterials, Institute of Clinical Sciences at University of Gothenburg (academic enrolment)
Envisioned start and duration: The doctorate will start in Q2 2021 and be funded for 4 full years thereafter.


Job description:


The topic of the PhD project is: "On a scientific basis for a novel bone-conduction hearing implant system".
The project will explore options for innovative bone conducting hearing implants in terms of design, material, bone and soft tissue response, as well as exploring anti-microbial strategies. The research activities are highly multidisciplinary, bringing together expertise from the life sciences (immunology, histology, microbiology, biochemistry, cellular and molecular biology), the physical sciences (mechanical engineering, materials science, bioengineering) and clinical sciences.

This industrial PhD project is an interdisciplinary collaboration between the Department of Biomaterials, Institute of Clinical Sciences, University of Gothenburg, and the Research & Technology department at Oticon Medical AB based in Gothenburg, Sweden. The PhD student will be fully embedded in both these departments. The University will provide scientific supervision and provide the methodological toolbox of techniques to study the bone and soft tissue surrounding the implants and abutments. Oticon Medical will provide supervision, access to health professionals networks and expertise in hearing science, device design, engineering, and manufacturing.
This is 4-year research position in the frame of a 4-year doctoral program (resulting in a PhD degree in Medical Science awarded by University of Gothenburg), funded by the Swedish Foundation for Strategic Research and the William Demant Foundation.


Requested expertise and eligibility criteria:


Candidates must hold a master’s degree in mechanical engineering, materials science, biomaterials, biotechnology, biomedical engineering, biomedicine, medical science, molecular biology or equivalent. The candidates must have excellent proficiency in the English language, as well as good communication skills, both oral and written.
Experience with biomaterial device design and evaluation, experimental molecular or microbiological tools and techniques, preclinical evaluation of biomaterials, histology and histomorphometry are substantial assets. Knowledge of immunohistochemistry, microbiology, cell biology, biomaterials and/or medical device development is meriting. Candidates should have an interest in biomaterials and engineering, and preclinical research and its relevance for translation of research into clinical application. Finally, candidates should have a willingness to deep dive into different solution spaces, setting up testing and analysis, demonstrate great motivation and a desire to excel in research dissemination.


Want to join our journey?


Interested candidates should submit (a) a cover letter describing their background, research experiences, interests, and goals (max 2 pages), (b) a curriculum vitae, (c) at least one letter of recommendation from previous research supervisors, (d) a copy of diploma (with the university transcripts), (e) English language certificate (e.g. IELTS, TOEFL). We only accept applications via our online recruitment system.
To learn more about the job, please contact Senior Translational Research Manager, Martin Johansson ([email protected], +46 736408010) or Assoc Professor Anders Palmquist ([email protected], +46 768979058). Deadline for applications is 10th of July 2021.


We are looking forward to hearing from you!



Because sound matters


Oticon Medical is a global company in implantable hearing solutions, dedicated to bringing the magical world of sound to people at every stage of life. As part of the Demant group, a global leader in hearing healthcare with 15,000 people in over 130 countries, we have access to one of the world’s strongest research and development teams, the latest technological advances and insights into hearing care.


Our competencies span more than a century of innovations in sound processing and decades of pioneering experience in hearing implant technology. We work collaboratively with patients, physicians and hearing care professionals to ensure that every solution we create is designed with users’ needs in mind. We share an unwavering commitment to provide innovative solutions and support that enhance quality of life for people wherever life may take them.
Because we know how much sound matters. Visa mindre

Developer Mechanics

Are you ready to make a difference for people with a severe hearing disability, and are you fueled by professional pride and curiosity? Are you skilled within the area of fine mechanics design and do you want to be part of developing new and innovative implantable hearing solutions? Then we can offer you an exciting opportunity as Mechanical Developer at Oticon Medical. We are a fast growing and agile company. We are ambitious and possess an entrepreneur s... Visa mer
Are you ready to make a difference for people with a severe hearing disability, and are you fueled by professional pride and curiosity? Are you skilled within the area of fine mechanics design and do you want to be part of developing new and innovative implantable hearing solutions?
Then we can offer you an exciting opportunity as Mechanical Developer at Oticon Medical.
We are a fast growing and agile company. We are ambitious and possess an entrepreneur spirit and the will to win. We offer an opportunity to join us on our exciting journey and to help us develop innovative implantable hearing solutions that improve the lives of thousands of children and adults across the globe. This job relates to the BAHS products and the role is situated in modern offices in Askim, right outside Gothenburg.
Successful in the job
For you to be successful in this job, we are looking on following skills and qualifications:
You are motivated by hands-on mechanical design and product development with a clear focus on customer needs, and by working in cross-professional development teams
You likely hold a BSc or MSc degree in mechanical engineering.
You are familiar with the most common mechanical manufacturing techniques
Either a few years’ experience working as developer, design engineer OR a genuine mechanical design interest.
Knowledge within Medical device development is an asset.
Experienced in CAD modeling, preferably Creo.
Well structured and good documentation skills.
Fluent in English (spoken/written)
A proper work-life balance is a key focus area in our organization and while flexibility goes both ways you are able to travel up to 20 days per year.

Responsibilities include
Micro-mechanical design – from requirements and concepts to products running in production
Product development and design deliverables, most often driven in project format.
3D CAD modelling
Design, build and test physical prototypes
Cost and production optimization of designs
Change order management support, meaning based on user or production input update designs and specifications for products.
Ensuring regulatory compliance of materials, designs and documentation.

Would you like to know more?
Then send your application and CV through our website latest on 8th of August, 2021. Interviews will take place throughout.
If you would like to know more about the position, you are welcome to contact Head of R&D on [email protected].
We are looking forward to hearing from you.
Öppen för alla
Vi fokuserar på din kompetens, inte dina övriga förutsättningar. Vi är öppna för att anpassa rollen eller arbetsplatsen efter dina behov. Visa mindre

Operations Quality Manager

Do you want to improve the life of people with a hearing disability? Are you a Quality Manager or Quality Engineer with passion for Production and Process control within the medical device area? Then we might have an exciting position for you as Operations Quality Manager at Oticon Medical BAHS in Gothenburg. At Oticon Medical BAHS we develop and market bone anchored hearing systems including active and non-active implants, sound processors, software and... Visa mer
Do you want to improve the life of people with a hearing disability? Are you a Quality Manager or Quality Engineer with passion for Production and Process control within the medical device area? Then we might have an exciting position for you as Operations Quality Manager at Oticon Medical BAHS in Gothenburg.

At Oticon Medical BAHS we develop and market bone anchored hearing systems including active and non-active implants, sound processors, software and various accessories. We are now looking to add a great new member to our Operations team were we, among other key tasks, are responsible for purchasing, production and logistics in collaboration with external partners.

As Operations Quality Manager, reporting to Head of Operations, you will be responsible for production and process control of all our outsourced production and distribution processes. You will be involved in setting up and maintaining production processes in collaboration with our suppliers as part of product development projects, supplier change projects and projects related to distribution and return flows. You ensure production quality of all our medical devices by securing that activities are well defined, planned, documented, and executed according to Medical Device standards and regulations, all in close collaboration with internal and external partners.

Your responsibilities
You will ensure production and process quality for all Oticon Medical BAHS products through outsourced partners.
Create input to production and process requirement specifications including traceability and handling procedures.
Develop and maintain specifications, instructions and procedures for production quality monitoring and release of products.
Develop process validation master plans, ensure establishment, and maintain process quality documentation.
Process owner of the sterilization process – E-beam & ETO
Drive CAPAs and follow up of corrective actions related to production and process performance.
Represent production and process control as subject matter expert during external audits.
Drive the supplier audit plan, execute audits as lead auditor, document, and follow-up.
Prepare yearly supplier evaluation reports including performance KPI´s.
Provide process performance data to management QMS review



Your experience and qualifications
You come along with a degree in Engineering and a minimum of 5 years of work experience, preferably related to production quality of high-class medical devices. You have through knowledge of MDSAP, ISO 13485 and GMP requirements. Experience from sterilization processes validation both E-beam & ETO is highly meriting.
You are stimulated by building relationships and implementing improvements and new processes as well as working in cross functional teams with your colleagues.
Your professional style is characterized by your ability to work structured and focused in a technical and professional manner.
Besides that, we expect that you are pragmatic and strive for efficiency in all that you do.
· You think and act holistically and like to take responsibility
· You are skilled in creating and maintaining good relations to all parts of the organization
· You know how to benefit from multi-site and multi-cultural development teams
Besides the above mentioned, we prefer flexible candidates who can travel up to 20 days per year.

We dare to make a difference
Together with skilled colleagues, you are part of a dynamic environment based on trust and openness, and you will experience a strong will to win. We are a growing international company where everybody supports the business by contributing to the customers’ experience of our products as the most attractive to work with. You will be working in a bright and open workplace, where a flexible working environment, knowledge sharing, and professional respect makes it both challenging and meaningful to go to work.
Would you like to know more?
Then send your application and CV through our online recruitment system latest on June 11, 2021. Please do not send us your application via e-mail.
If you would like to know more about the position, you are welcome to contact Head of Operations Niklas Aulin on [email protected].
We are looking forward to hearing from you.

Oticon Medical is part of Demant group with more than 14.500 employees across the world. Oticon Medical is the fastest growing manufacturer of bone anchored and cochlear implant hearing systems for children and adults. At Oticon Medical we combine more than a century of experience in audiology and sound processing from Oticon with decades of pioneering experience in hearing implant technology. Our connection to Oticon gives us unique access to knowledge, resources and technology that we use for developing innovative and life-changing implantable hearing Visa mindre

Operations Project Manager

Do you want to improve the life of people with a hearing disability? Are you a Project Manager with passion for Production within the medical device area? Then we might have an exciting position for you as Operations Project Manager at Oticon Medical BAHS in Gothenburg. At Oticon Medical BAHS we develop and market bone anchored hearing systems including permanent implants, sound processors, software and various accessories. We are now looking to add a grea... Visa mer
Do you want to improve the life of people with a hearing disability? Are you a Project Manager with passion for Production within the medical device area? Then we might have an exciting position for you as Operations Project Manager at Oticon Medical BAHS in Gothenburg.
At Oticon Medical BAHS we develop and market bone anchored hearing systems including permanent implants, sound processors, software and various accessories. We are now looking to add a great new member to our Operations team were we, among other key tasks, are responsible for purchasing, production and logistics in collaboration with external partners.
As Operations Project Manager, reporting to Head of Operations, you will work with development of new products but also drive projects within the Operations function and changes of in-market products.
In development projects you will be accountable for the operations part and an important member of the project core team, headed by a Senior Project Manager. You will be a key player in making sure that the product is manufactured in time, with correct quality and ready to be shipped to various distributors worldwide. You will act as an important link between R&D and the external production facility and drive the transfer of information to prepare for a smooth transition from project phase to serial production.

Main responsibilities
Represent Operations in product development projects and be accountable for all operations deliverables according to the project delivery list;
Design input related to Operations
Supplier & logistics set-up
Act as link between R&D and external suppliers/production sites
Manufacturing set-up, production flow and establishment and qualification of all processes
Creation, approval, and communication/transfer of DMR; manufacturing specifications, instructions and BOM structures
Drive the launch planning activities related to Operations such as capacity, phase-in/phase-out & volume planning
Ensure distribution systems readiness
Drive projects within Operations
Drive change projects related to in-market products


Your experience and qualifications
You come along with a degree in Engineering and a minimum of 5 years of work experience, preferably related to project management & manufacturing of medical devices. You have a structured and professional way of working and a good technical understanding and interest of products and production environment.
You are stimulated by building relationships and working in cross functional teams with colleagues and suppliers.
Besides that, we expect that you are pragmatic and strive for efficiency in all that you do.
You think and act holistically and like to take responsibility
You are skilled in creating and maintaining good relations to all parts of the organization
You know how to benefit from multi-site and multi-cultural development teams



We prefer flexible candidates who can travel up to 20 days per year since our collaboration partners for development, distribution and production are situated in Sweden, Denmark, Poland & France.
We dare to make a difference
Together with skilled colleagues, you are part of a dynamic environment based on trust and openness, and you will experience a strong will to win. We are a growing international company where everybody supports the business by contributing to the customers experience of our products as the most attractive to work with. You will be working in a bright and open workplace, where a flexible working environment, knowledge sharing, and professional respect makes it both challenging and meaningful to go to work.
Would you like to know more?
Then send your application and CV through our online recruitment system latest on June 25, 2021. Please do not send us your application via e-mail.
If you would like to know more about the position, you are welcome to contact Head of Operations Niklas Aulin on [email protected].
We are looking forward to hearing from you. Visa mindre

Quality Complaint & Product Return Manager

Quality Complaint & Product Return Manager for Oticon Medical BAHS, Gothenburg Do you want to improve the life of people with a hearing disability? Are you an Engineer with passion for quality and technology? Then we might have an exciting position for you as Quality Complaint & Product Return Manager at Oticon Medical BAHS in Gothenburg. At Oticon Medical BAHS we develop and market bone anchored hearing systems including implants, sound processors, softw... Visa mer
Quality Complaint & Product Return Manager for Oticon Medical BAHS, Gothenburg
Do you want to improve the life of people with a hearing disability? Are you an Engineer with passion for quality and technology? Then we might have an exciting position for you as Quality Complaint & Product Return Manager at Oticon Medical BAHS in Gothenburg.
At Oticon Medical BAHS we develop and market bone anchored hearing systems including implants, sound processors, software and various accessories. We are now looking to add a great new member to our joint QARA, Operations and Product care organization were we among other key tasks, are responsible for regulatory compliance, quality management system, complaint handling, production and change management of all in-market products.
You will be responsible for all aspects of complaint handling, vigilance reporting and product returns, and report directly to the Senior Director, QARA & Operations.
Complaint handling and vigilance reporting are key processes in the company ensuring that we have safe and reliable products on the market. That we react to upcoming problems in a fast and structured way. And that we support our customers and users with an efficient service process ensuring they always have access to sound. In addition, we secure that we are following global regulatory requirements on vigilance reporting.
Your responsibilities
You have the overall responsibility for the complaint, vigilance and return processes, where you drive process improvements and represent the areas in audits as process owner and subject matter expert.
Furthermore, your tasks will be:
Define and be accountable for all procedures and instructions for own areas
Ensure efficient reporting of complaints from the market through training and support to worldwide distributors
Conduct technical investigations of all product related complaints (Bone anchored implants, sound processors and accessories)
Support and train technicians in our Polish production site in technical investigations of product returns for service
Drive complaint root cause investigations with different stakeholder and suggest corrective and preventive actions
Establish documentation related to all complaints
Prepare vigilance reports to different markets according to regulatory requirements
Efficient communication to worldwide distributors related to complaints
Prepare trending reports, analyze statistics, drive required actions and ensure input to product development
Conduct Quality Surveillance programs
Host complaint meetings with global distributors and internal stakeholders
Maintain the complaint system
Define and ensure implementation of an efficient product return system


Your experience and qualifications
You come along with a degree in Engineering and a minimum of 5 years of work experience within the field of Quality, R&D, production, or product support in the medical devices industry. You have an analytical, thorough, and structured approach to problem solving and take full responsibility of your business area. As we are a networking community, you should like to share your knowledge and ideas with the team and across the organization and have excellent skills in communicating with many stakeholders.
We expect that you have technical and analytical skills to investigate and determine failure of the products investigation, and understand the regulatory requirements related to complaint handling and vigilance reporting for high class medical devices.
We dare to make a difference
Together with skilled colleagues, you are part of a dynamic environment based on trust and openness, and you will experience a strong will to win. We are a growing international company where everybody supports the business by contributing to the customers’ experience of our products as the most attractive to work with. You will be working in a bright and open workplace, where a flexible working environment, knowledge sharing, and professional respect makes it both challenging and meaningful to go to work.
Would you like to know more?
Then send your application and CV through our online recruitment system as soon as possible and no later than 1st of December 2020. Please do not send us your application via e-mail.
If you would like to know more about the position, you are welcome to contact Senior Director Karolin Isberg Jernby on [email protected].
We are looking forward to hearing from you.
Because sound matters
Oticon Medical is a global company in implantable hearing solutions, dedicated to bringing the magical world of sound to people at every stage of life. As part of the Demant group, a global leader in hearing healthcare with 15,000 people in over 130 countries, we have access to one of the world’s strongest research and development teams, the latest technological advances and insights into hearing care.
Our competencies span more than a century of innovations in sound processing and decades of pioneering experience in hearing implant technology. We work collaboratively with patients, physicians and hearing care professionals to ensure that every solution we create is designed with users’ needs in mind. We share an unwavering commitment to provide innovative solutions and support that enhance quality of life for people wherever life may take them.
Because we know how much sound matters. Visa mindre

Mechanical Design Engineer to Medical implant devices - maternity cover

Ansök    Apr 9    Oticon Medical AB    Industridesigner
Are you ready to make a difference for people with a severe hearing disability, and are you fueled by professional pride and curiosity? Are you skilled within the area of fine mechanics design and do you want to be part of developing new and innovative implantable hearing solutions? Then we have an exciting opportunity for you as a Mechanical Engineer – join us on our exciting journey and help us develop innovative implantable hearing solutions that improv... Visa mer
Are you ready to make a difference for people with a severe hearing disability, and are you fueled by professional pride and curiosity? Are you skilled within the area of fine mechanics design and do you want to be part of developing new and innovative implantable hearing solutions?
Then we have an exciting opportunity for you as a Mechanical Engineer – join us on our exciting journey and help us develop innovative implantable hearing solutions that improve the lives of thousands of children and adults across the globe.
Oticon Medical is a leading company within Bone Anchored Hearing Systems (BAHS) and Cochlear Implants (CI) with development in both Gothenburg, Sweden and Smørum, Denmark. We are a fast growing, agile company with ambitions and we possess an entrepreneur spirit and the will to win. Likewise, we are part of a large international organization within Demant.
As Mechanical Engineer, you will be based in Gothenburg and part of Oticon Medical BAHS R&D. Our project activities are, however, distributed across several sites - Gothenburg, Smørum, Nice and Stettin - so multi-site cooperation will be a natural part of your daily work.

What does that mean?
You will have the opportunity to work with project activities that cover both development of new products and investigation and preparation of new technologies, and our project teams are typically multi-disciplinary and can include R&D, Operations, Regulatory, Clinical as well as Marketing.
For our implant projects, the core development team will typically be located in Gothenburg and your main responsibilities will be;
Mechanical design – from requirements and concept to products running in production
Idea creation and design management
Design documentation and design reviews
Secure technical validity and manufacturability of the designs

How to be a success in the job
We are looking for an easy-going person who are able to communicate with colleagues and multiple stakeholders from various technical and business background. You are solution oriented, ambitious and driven to succeed. You are self-motivated, flexible and positive person that are energized by working in a multidisciplinary and international team environment.
You have a B.Sc. or an M.Sc. engineering degree and technical knowledge and experience of working with technical documentation and 2D and 3D design. If you have experience with working in hardware development projects and an understanding of manufacturing processes in fine mechanics, preferably within plastics and metal, that would all be an advantage. Experience of working in a medical device company or other regulated industry will also be an advantage.
Our company language is English, so fluency in English, written as well as orally, is a must.
We dare to make a difference
We offer you a great opportunity to make a difference – and put your mark on tomorrows hearing solutions. We are at the forefront of the latest technology, constantly working to improve our products and this has led us to a point where we have a portfolio of top of the line products – and some of the best employees in the field.
You will be seizing an opportunity to be part of a growing international company with a dynamic environment built on trust and openness and a strong will to win.


Apply & Join us
Send your application and CV in English no later than April 26th, 2021. Please note that we only accept applications via our online recruitment system and that we screen applications continuously.
If you would like to know more about the position, please contact Hanna Peters, Head of PBAHS Surgical at +0046 (0)763 458 238 or [email protected].
We look forward to hearing from you.
Because sound matters
Oticon Medical is a global company in implantable hearing solutions, dedicated to bringing the magical world of sound to people at every stage of life. As part of the Demant group, a global leader in hearing healthcare with 15,000 people in over 130 countries, we have access to one of the world’s strongest research and development teams, the latest technological advances and insights into hearing care.
Our competencies span more than a century of innovations in sound processing and decades of pioneering experience in hearing implant technology. We work collaboratively with patients, physicians and hearing care professionals to ensure that every solution we create is designed with users’ needs in mind. We share an unwavering commitment to provide innovative solutions and support that enhance quality of life for people wherever life may take them.
Because we know how much sound matters. Visa mindre

Product Manager

Global Product Manager Surgery BAHS – position located in Sweden, Sisjön Oticon Medical is committed to improve the quality of life of profoundly deaf patients. For that, we develop implantable medical devices and surgical techniques to restore profound hearing loss. As a member of one of the world’s largest groups of hearing health care companies, we share a close link with Oticon and direct access to the latest advancements in hearing research and tech... Visa mer
Global Product Manager Surgery BAHS – position located in Sweden, Sisjön

Oticon Medical is committed to improve the quality of life of profoundly deaf patients. For that, we develop implantable medical devices and surgical techniques to restore profound hearing loss. As a member of one of the world’s largest groups of hearing health care companies, we share a close link with Oticon and direct access to the latest advancements in hearing research and technologies. Our competencies span more than a century of innovations in sound processing and decades of pioneering.

We are very ambitious and have a strong entrepreneur spirit and the will to win. Join us on our exciting journey and help us develop and commercialize innovative implantable hearing solutions that improve the lives of thousands of children and adults across the globe.

We are looking for a Global Product Manager BAHS (Bone Anchored Hearing Systems) for our office in Sweden. The Product Management team BAHS consists of 6 persons including the new hiring and reports directly to the Director, Product Management BAHS in Gothenburg. We offer you a very interesting and challenging opportunity to be a part of an international growth company with a strong product roadmap. The right candidate has a strong surgical background, a genuine interest in hearing solution technology and a deep understanding for our users needs. You should also be ambitious, driven and motivated by making a difference to improve our users hearing experience.

Purpose 
?   Based on strong market understanding, Product Management shall define user experiences that lead to attractive, commercially relevant and prioritized products.
?   Our product strategy and product development are based on thorough market insight, data and knowledge coming from internal cross-functional collaboration and external sources.

Key Tasks & Responsibilities  
?   Ensure a strong product offer to the market through effective product marketing, communication and support 
?   Very close collaboration with R&D throughout the development phases
?   Responsible for marketing deliverables in P2M process
?   Define/develop product labeling and packaging requirements
?   Responsible for claims management of own products
?   Close collaboration with Clinical creating evidence and claims to drive strong campaigns
?   Drive product lifecycle with clear priorities to the organization
?   Define/develop mandatory documents for new products and ensure improvements to existing products
?   Develop sales & marketing strategies and responses to competitive product launches
?   Explore and support the education and training needs for new product launches and other marketing activities including developing, delivering and giving training presentations
?   Competitor surveillance; collect, analyze and summarize competitor information in selling against documents

Travelling Requirement 
Travel required to support international conferences, launch events, training and sales support

Travel time estimated at 30-50 days per year.

Education     
You may hold a relevant degree in marketing / business administration. You have 5+ years of experience with Product Management or Marketing focused positions within this area. Experience working in a clinic, with sales or in an international company would be an advantage.

Personal & Social competencies 
In order for you to succeed in this position, you need to have excellent communication, coordination and stakeholder management skills, as you need to engage with colleagues across different business arears.


You are analytical and fact based, preferably you have experience from working within tech. Moreover, you need to have a strategic mindset and be goal and result oriented. We expect you to have profound English language skills, being our Company language.

Do you want to join the team?
Then send us your application as soon as possible, no later than 9th of February 2020. Applications will be considered on an ongoing basis.
The application needs to be submitted via our online Recruitment system. We do not accept applications by e-mail.
 
Recruitment agency? Thank you for your interest, but we are sourcing all our candidates directly or via our preferred suppliers. We appreciate you trying but please keep in mind that any unsolicited profiles you send us will be treated as direct applications from the candidates Visa mindre

Senior Project Manager

We see it as our goal and purpose to improve people’s quality of life, helping them gain or regain hearing ability through our advanced hearing implants. Did you know for example that there is a proven close relation between hearing impairment and dementia?  Join us in our journey to make a difference for thousands with hearing impairment.    Lead a large strategic important project  Your role will be to lead and drive our most strategic and advanced devel... Visa mer
We see it as our goal and purpose to improve people’s quality of life, helping them gain or regain hearing ability through our advanced hearing implants. Did you know for example that there is a proven close relation between hearing impairment and dementia? 
Join us in our journey to make a difference for thousands with hearing impairment. 
 
Lead a large strategic important project 
Your role will be to lead and drive our most strategic and advanced development projects within bone anchored hearing solutions. You will be fully responsible for planning and executing from concepts to successful release to the market. You will be part of a team of Project Managers leading all projects in Oticon Medical covering both Bone Anchored Hearing Implants and Cochlear Implants. 


As Senior Project Manager, you will be part of Oticon Medical’s R&D organization, reporting to the Vice President of R&D. 
 
The position is either based at our Oticon Medical office in the Nice area or at our office in Gothenburg. The project activities distributed across several sites, so multi-site project management will be a natural part of your daily work. 
 
Furthermore, your key responsibilities include 
Ensure deliveries comply to medical, regulatory and internal quality requirements 
Project reporting and milestone reviews according to our quality management system 
Ensure we make the right compromises and decisions both on overall product scope and down to technical specifications 
Pro-active stakeholder management - both internally and to external partners or subcontractors 
Leading the project team of skilled development engineers and project managers 

 
Your background 
In order to be a success in this role, it is vital that you have the following skills and qualifications: 
A B.Sc. or an M.Sc. engineering degree or similar technical background 
A minimum of 5 years of experience in management of product development projects/programs, 
Experience from working with cross-functional teams across multiple sites 
Fluency in English (spoken/written)

 
Experience from medical device development and medical device standards will be an advantage. Similarly, we prefer candidates with a technical background from companies developing similar products. 
 
Your footprint 
To be a match in this role, it is crucial that you understand the importance of ensuring deliveries on-time and handling multiple stakeholders. This means that you are result driven and capable of setting clear goals for yourself and your team; create a strong team spirit across multiple locations and departments. You know how to lead and motivate your project team towards success. 
 
Furthermore, you have a general technical insight and curiosity to support a multi-disciplinary work environment in developing as well as market a high-tech medical device system. 
 
We offer a driven and ambitious culture in our endeavors to reach our goals. We show flexibility and expect you to do the same. Since we are a global company working across sites, you should be able to travel app. 50 days per year. 
 
Finally, we are a growing organization with high ambitions and therefore it is important that you have the drive and ability to contribute to a continuous improvement of the ways we work. 
 
We believe in the good life 
Oticon Medical offers many challenges in an international organization full of energy and expertise. The right candidate will learn very much in a short time span, since you will have the opportunity to work with all aspects of clinical studies. Personal and professional development is the foundation for the growth of our business.
 
We create solutions that allow people to live their lives to the fullest. We also recognize that in order to bring energy and inspiration to work, you need to re-energize and spend time with family, friends and hobbies in a healthy work life balance. 
  
Application and contact 
To learn more about the job, please contact Vice President, Klaus Svendsen on +45 29220277 Please send your application and CV online only and no later than 3 January 2020. 
 
About Oticon Medical 
Oticon Medical is a global company in implantable hearing solutions, dedicated to bringing the magical world of sound to people at every stage of life. We are part of the Demant Group - one of the world’s largest groups of hearing health care companies with more than 14,500 employees worldwide and revenues of over DKK 14 billion. We share a close link with Oticon and have direct access to the latest advancements in hearing research and technologies. Our competencies span more than a century of innovations in sound processing and decades of pioneering experience in hearing implant technology. By working collaboratively with patients, physicians and hearing care professionals, we ensure that every solution we create is designed with user needs in mind. We share an unwavering commitment to provide innovative solutions and support that enhance quality of life for people wherever life may take them. Because we know how much sound matters. Visa mindre

System Engineer for Gothenburg or Denmark

Join us in making a difference for our users and patients by developing products for hearing impaired. If you thrive with analyzing and structuring system aspects as well as facilitating initiatives and individuals, then we might have the job for you. As a quick overview of the tasks you will be taking care of are: Leading architectural initiatives and technical system related analysis Developing and maintaining BAHS system architectures, requirements an... Visa mer
Join us in making a difference for our users and patients by developing products for hearing impaired. If you thrive with analyzing and structuring system aspects as well as facilitating initiatives and individuals, then we might have the job for you.


As a quick overview of the tasks you will be taking care of are:
Leading architectural initiatives and technical system related analysis
Developing and maintaining BAHS system architectures, requirements and verification specifications
Participate in the risk management and usability engineering activities, etc.



System Engineering
We are looking for system engineer for our department System Engineering in R&D. The position is situated in either Denmark (Smørum) or in Sweden (Gothenburg).


Your core responsibility in the team will be to develop and maintain our Bone Anchored Hearing System (BAHS) requirements, -architecture and -verification specifications to support needs in our product development and in alignment with our product roadmap. We work close to our colleagues in Oticon Medical to efficiently leverage from new chipsets and innovations from Oticon in the Oticon Medical BAHS product line.


Your closest collaboration in your work day will be the team of architects across sites as well as the project managers and product management, R&D and Quality/Regulatory functions. We promise you that you will have a broad interface with different departments.


You will focus on innovation, performance and safety and will interface with other function engineers (electronic, mechanical, software, firmware, test), Quality/Regulatory as well as Engineering, Project Management, Product Marketing and Clinical teams.


An everyday could look like participation in different product development projects where your role is both having an executing and advising role.
You will help project managers on project planning related to system aspects, e.g. identifying dependencies, etc.


Furthermore, you will drive information, training and other initiatives to roll-out and maintain systems engineering skills and mindset in Oticon Medical.
 
Technical background
You hold a master degree in engineering within electronics, software or similar, and you are motivated by system engineering.


You have demonstrated experience of 5 years in a preferably industrial regulated environment with broad exposure to hardware / software / system design.


To be able to thrive in this position, you have a profound system modelling skills and are comfortable breaking down complex systems and negotiating the right interfaces.
Ideally, you have experience with tools- and methodologies for systems engineering, like e.g. SySML.


Being part of a global company, you are fluent in English (both spoken and written).


We offer a flexible working environment where you will have the ability to plan your up to 30 travel days per year.


Strong interpersonal and communication skills
In this role, you will collaborate with a multitude of internal stakeholders from the Swedish, Danish, and French part of the organization. This means you can look forward to working in a dynamic international business environment alongside lots of great people where you will be in a position to influence and drive business and get results.


You thrive at interacting with many stakeholders and know that defining requirements and architecture is very much about communication and involvement of the right people and about finding good compromises.


You have a passion for creating the system overview and setting the systems into a broader context. You have interpersonal and leadership skills, possess systems thinking and have a strong product development understanding.


We dare to make a difference
Together with skilled colleagues, you are part of a dynamic environment based on trust and openness, and you will experience a strong will to win. We are a growing international company where everybody supports the business by contributing to the customers’ experience of our products as the most attractive to work with. You will be working in a bright and open workplace, where a flexible working environment, knowledge sharing and professional respect makes it both challenging and meaningful to go to work.


Want to join us?
Then send your application as we are continuously screening applications and not later than 27 November 2019. Apply for the job via www.oticonmedical.com


For questions regarding the position please contact Sr Director Eric Pepin Lehalleur ([email protected])


We look forward to hearing from you.


About us
Oticon Medical is a global company in implantable hearing solutions, dedicated to bringing the magical world of sound to people at every stage of life. We are part of the William Demant Group - one of the world’s largest groups of hearing health care companies with more than 14.500 employees worldwide and revenues of over DKK 14 billion. We share a close link with Oticon and have direct access to the latest advancements in hearing research and technologies. Our competencies span more than a century of innovations in sound processing and decades of pioneering experience in hearing implant technology. By working collaboratively with patients, physicians and hearing care professionals, we ensure that every solution we create is designed with user needs in mind. We share an unwavering commitment to provide innovative solutions and support that enhance quality of life for people wherever life may take them. Because we know how much sound matters. Visa mindre

Clinical Trial Manager (maternity cover)

Join us in making a difference for our users and patients within clinical trials. We are looking for someone to join us for a maternity cover starting in January, 2020. You will help us build clinical documentation for our current Bone Anchored Hearing System (BAHS) and new developments. You can also look forward to be part of bringing new products to the market – and work with the clinical trials that allows that. Based at Oticon Medical AB in Ask... Visa mer
Join us in making a difference for our users and patients within clinical trials. We are looking for someone to join us for a maternity cover starting in January, 2020.
You will help us build clinical documentation for our current Bone Anchored Hearing System (BAHS) and new developments. You can also look forward to be part of bringing new products to the market – and work with the clinical trials that allows that.
Based at Oticon Medical AB in Askim, Sweden you will become part of an interdisciplinary environment at Oticon Medical’s offices in Gothenburg and Copenhagen, Denmark.


You plan and conduct clinical trial activities
In your new temporary position (12 months) as a Clinical Trial Manager, you will play a key role with responsibility for planning and conducting sponsored clinical trial activities with focus on BAHS implants and surgical aspects. You work closely together with our R&D, QA/RA and marketing groups. You also take part in building relationship with and connecting to researchers in the field.
Moreover, you will be involved in further improvements of the internal processes and procedures for clinical trials.
 
Summed up, you will be responsible for the following tasks:
Planning and execution of clinical trials within the area of BAHS implants and surgery
Write study documentation
Write documentation for study approval by ethical committee and competent authorities
Ensure documentation for clinical trials are complete and up-to-date
Ensure or carry out relevant monitoring activities
Perform data management tasks
Analyze data and conduct statistical analyzes
Take part in developing our procedures for clinical trials and related activities

 
Your profile will help deciding the exact tasks you will work with, but the job will be varying, stretching from strategic directions to the hands-on execution of clinical trials.
You can expect 20-40 days of business travel per year.


Experience with clinical trials
The ideal candidate will have the following qualifications:
Relevant academic background (typically a Master’s degree in biomedicine, biomaterials, engineering or similar)
Experience with designing and preparing documentation for clinical trials of medical devices, ideally having worked in a medical device company or CRO
Experience with both pre- and post-market clinical trials
Experience in monitoring
Good working knowledge of relevant regulations, e.g. ISO14155
Good communication skills, and speak and write English proficiently

 
Moreover, we hope to see the following skills in your CV:
Previous work in an R&D setting, where products and ideas are constantly evolving
Knowledge of bone anchored or other hearing devices
Statistical knowledge and skilled at statistical analysis
Experiences from negotiating contracts on clinical studies
Research experience in a relevant academic field

 
We are looking for a team player who finds it inspiring to discuss challenges with colleagues, but who can also initiate and conduct tasks by him/herself. You have a scientific approach, and you also acknowledge the business point of view. You are pragmatic, results oriented and get things done. You have an eye for the detail as well as an overview.
 
Even if you don’t have all competences and experiences above, we would like to hear from you.
 
Our offer to you
Oticon Medical offers many challenges in an international organization full of energy and expertise. The right candidate will learn very much in a short time span, since you will have the opportunity to work with all aspects of clinical trials. You will be part of an environment based on trust and openness. We offer flexible working conditions.
 
Application and contact
To learn more about the job, please contact Director, Clinical Affairs, Surgical Systems, Sofia Jonhede ([email protected]: phone: +46763286731). Please send your application and CV via www.oticonmedical.com. NB! Deadline is 27 November, 2019
Read more about Oticon Medical on www.oticonmedical.com
 
About Oticon Medical
Oticon Medical is a global company in implantable hearing solutions, dedicated to bringing the magical world of sound to people at every stage of life. We are part of the Demant Group - one of the world’s largest groups of hearing health care companies with more than 14,000 employees worldwide and revenues of over DKK 14 billion. We share a close link with Oticon and have direct access to the latest advancements in hearing research and technologies. Our competencies span more than a century of innovations in sound processing and decades of pioneering experience in hearing implant technology. By working collaboratively with patients, physicians and hearing care professionals, we ensure that every solution we create is designed with user needs in mind. We share an unwavering commitment to provide innovative solutions and support that enhance quality of life for people wherever life may take them. Because we know how much sound matters. Visa mindre

Gothenburg Senior Mechanical Developer for Oticon Medical , Gothenburg

Have you ever considered that you could make true difference for people with hearing impairment world wide by helping us achieve our purpose which is: Sound matters?You bring your skillset in mechanics from medical device development and we have the goal. Join us to develop new and innovative implantable hearing solutions that truly matters for people.At Oticon Medical, we develop both Bone Anchored Hearing Systems (BAHS) and Cochlear Implants (CI). We are... Visa mer
Have you ever considered that you could make true difference for people with hearing impairment world wide by helping us achieve our purpose which is: Sound matters?You bring your skillset in mechanics from medical device development and we have the goal. Join us to develop new and innovative implantable hearing solutions that truly matters for people.At Oticon Medical, we develop both Bone Anchored Hearing Systems (BAHS) and Cochlear Implants (CI). We are a fast growing and agile company. We are ambitious and possess an entrepreneur spirit and the will to win. We offer an opportunity to join us on our exciting journey and to help us develop innovative implantable hearing solutions that improve the lives of thousands of children and adults across the globe.Successful in the jobAs Senior Mechanical Developer, you will be based in Gothenburg and part of Oticon Medical R&D - consisting of 3 development sites; Smørum in Denmark, Gothenburg in Sweden and Vallauris on the French Rivera. In general, as Sr. Mechanical developer in Oticon Medical, your focus will be to find technical solutions, balance requirements and act as technical lead and give guidance in your areas of your expertise. You are also expected to independently plan, organize and drive tasks within projects, early research or maintenance related topics.  More specifically in this role you will play a key role in our next generation of implanted solutions, this in close collaboration with all our sites in Europe, in doing so you are required to help navigate and balance both technical, regulatory and practical tasks.   For you to be successful in this job, we are looking on following skills and qualifications:At least 10 years’ experience working in development projects.Experience from being project manager and/or technical lead of a development projectsExperience working with medical device projectsKnowledge about biocompatibility, testing against standards is strongly meritingExperienced working with technical documentationHave very good communication skills is of essence in our international contextFluent in English (spoken/written)Likely a B.Sc. or an M.Sc. degree in mechanical, electrical engineering or similar Oticon Medical is a growing company and we are always looking for talented people, do you lack the seniority that this role requires don’t hesitate to send in your unsolicited application. Qualified?It is said that smiling makes you happier and enhances your chance to live longer. Your approach is to deal with challenges with a positive attitude and a smile; a trait we encourage in our company. You are cable of handling uncertainties and from time to time situations under pressure. We provide a dynamic working environment where adapting to new situations is vital.You bring a solid project management toolbox with you which enables you to set a clear direction, achieving your results by leading and motivating others. The projects you have led in the past have been cross-functional, working with R&D functions such as hardware, software, electro-acoustical or mechanical development. Your approach is constructive, structured and systematic, and you make an impact through clear communication. How to join us?You should be a flexible and positive person that thrives from team work  How to become part of us?We are screening applications continuously, and would like to receive your application not later than 30th of September 2019.For questions regarding the position, please contact Erik Holgersson on [email protected] Questions about the recruitment process contact Ditte Mi Petræus through [email protected] About Oticon MedicalOticon Medical is a global company in implantable hearing solutions, dedicated to bringing the magical world of sound to people at every stage of life. We are part of the Demant Group - one of the world’s largest groups of hearing health care companies with more than 14.500 employees worldwide and revenues of over DKK 14 billion. We share a close link with Oticon and have direct access to the latest advancements in hearing research and technologies. Our competencies span more than a century of innovations in sound processing and decades of pioneering experience in hearing implant technology. By working collaboratively with patients, physicians and hearing care professionals, we ensure that every solution we create is designed with user needs in mind. We share an unwavering commitment to provide innovative solutions and support that enhance quality of life for people wherever life may take them. Because we know how much sound matters. Visa mindre

Product Management Coordinator

Ansök    Sep 11    OTICON MEDICAL AB    Backofficepersonal
Are you motivated by new the development of commercial and bringing world-class product solutions to market in the MedTech field? Do you want to lead smaller projects in close collaboration with the graphics team, R&D, group services, and operations? If you can answer yes to these statements then you might just be the candidate we’re looking for! Because sound mattersOticon Medical’s hearing implant solutions benefit people wit... Visa mer
Are you motivated by new the development of commercial and bringing world-class product solutions to market in the MedTech field? Do you want to lead smaller projects in close collaboration with the graphics team, R&D, group services, and operations? If you can answer yes to these statements then you might just be the candidate we’re looking for! Because sound mattersOticon Medical’s hearing implant solutions benefit people with hearing loss, specialized to meet the needs of those who face the hardest hearing challenges. We are a fast-growing and agile company. We are very ambitious and have a strong entrepreneur spirit and the will to win. Join us on our exciting journey and help us develop and commercialize innovative implantable hearing solutions that improve the lives of thousands of children and adults across the globe. Tasks at handWe are looking for a Product Management Coordinator BAHS (Bone Anchored Hearing Systems) for our Gothenburg office. You are offered to join an interesting and challenging opportunity to be a part of an international growth company with a strong product roadmap. You will play a key factor in the success of our product management team by supporting them with different tasks. We want you to elevate and if you find it motivation, we would like you to drive the development of commercial and regulatory materials. Furthermore, you will be responsible for releasing marketing and mandatory materials in the document management system. Other responsibilities:Administration within releases (CR/CO procedure) for MarketingProject lead on smaller projects (packaging, demo articles, etc.)Support product campaigning and BAHS treatment communicationSupport in preparation for training, congresses and meetings (internal and external)Driving tasks related to the Go2Market processPerform desk-top market research and market analysis Travelling is required in this position, the trips will mainly be to our Danish site but international travels may occur since we are a global company.You will be reporting directly to the Director of Product Management BAHS. The match we are looking forYou should thrive in working in a complex and dynamic organizations engaging with different stakeholders. You have an interest in working structured and detail oriented to make sure that the processes are well organized.Probably, you have 1-2 years of experience in project coordination role. We consider it a plus if you have already knowledge in working with document handling systems and engineering and manufacturing processes. It is an advantage if you have experience in working in an international setting.Being part of a global company you should work effortlessly in English. ProcessWe are screening applications continuously, and would like to receive your application not later than 9 October 2019.For questions regarding the position, please contact Karin Humble on [email protected] Questions about the recruitment process contact Ditte Mi Petræus on [email protected] Visa mindre

Project Manager , Quality & Operations to Oticon Medical

Oticon Medical is part of Demant group with more than 14.000 employees across the world. Oticon Medical is the fastest growing manufacturer of bone anchored and cochlear implant hearing systems for children and adults. At Oticon Medical we combine more than a century of experience in audiology and sound processing from Oticon with decades of pioneering experience in hearing implant technology. Our connection to Oticon gives us unique access to knowledge, r... Visa mer
Oticon Medical is part of Demant group with more than 14.000 employees across the world. Oticon Medical is the fastest growing manufacturer of bone anchored and cochlear implant hearing systems for children and adults. At Oticon Medical we combine more than a century of experience in audiology and sound processing from Oticon with decades of pioneering experience in hearing implant technology. Our connection to Oticon gives us unique access to knowledge, resources and technology that we use for developing innovative and life-changing implantable hearing Would you like to work with products that actually change the lives of people worldwide and do it in a fast-growing company? Then you may be a good match for Oticon Medical. Right now, we are looking for a dedicated and highly skilled Project Manager for Quality and Operations related projects to support our fast-growing business and international expansion. What you are getting intoThe position is situated in our Gothenburg office working with Bone Anchored Hearing Systems (BAHS). In your new job, you will drive projects related to Quality and Operations. Assignments could include; Implementation of QMS related systems or new functionalities in existing systems (EDMS, CAPA, PLM,…) Operations and logistics improvements and projects related to distribution and return flows.Implementation of new regulationsMapping and defining QMS landscapeIdentify and utilize QMS synergies between entities in the Demant group to ensure smooth integration between collaboration partners You will be reporting to Senior Director QARA & Operations and be part of a function consisting of the RA team, the QA team, Product Maintenance team and the Operations team all with dedicated and highly skilled colleagues. The function is responsible for the Quality Management System (QMS), Regulatory Affairs, complaint handling and all aspects of manufacturing and logistics as well as maintenance of products released to market. Besides your closest colleagues you will be working closely together with other functions and external partners in different projects. Competences we are looking forWe are looking for someone with a passion to work with improvements and has an ability to keep a holistic view and strive for simplified and efficient processes. Basically, you have an engineering degree or similar. You have strong knowledge in medical device quality system standards (ISO 13485, MDSAP, MDD/AIMDD/MDR, QSR) and experience in medical device QMS supporting systems. You have project management skills, drive and people skills. Your approach is to deal with challenges with a positive attitude and a smile; a trait we encourage in our company. You think holistically and keep a good structure to your tasks.Furthermore, you know the value of building relationships and implementing improvements and new processes as well as working with cross functional teams. You are cable of handling uncertainties and from time to time situations under pressure. We provide a dynamic working environment where adapting to new situations is vital. Besides that, we expect that you are pragmatic and strive for efficiency in all that you do.As we are an international company, you can expect travel activity up to 40 days per year. Want to see from our side?To apply for this position please attach your CV and personal letter in English. For more information please contact Karolin Isberg Jernby +46 (0)703 551 459 Summer vacation is about to reach and we are open for applications until 10 August 2019. NB! We only accept applications via our online system. You can find more info on www.oticonmedical.com Visa mindre

Regulatory Affairs Country Specialist

Making people hear again with our bone-conducted hearing solutions is a truly amazing technology and goal. We aim to better life quality because we believe that sound matters. If you truly want to make a difference for people with hearing disability, then this is your opportunity. Our background storyOticon Medical AB is part of Demant Group. Demant is a world-leading hearing healthcare group that offers solutions and services to help people with hearing l... Visa mer
Making people hear again with our bone-conducted hearing solutions is a truly amazing technology and goal. We aim to better life quality because we believe that sound matters. If you truly want to make a difference for people with hearing disability, then this is your opportunity. Our background storyOticon Medical AB is part of Demant Group. Demant is a world-leading hearing healthcare group that offers solutions and services to help people with hearing loss connect and communicate with the world around them. For more than a century, the Demant Group has played a vital part in developing innovative technologies and know-how to help improve people’s hearing and health. In every aspect, from hearing devices, hearing implants and diagnostic equipment to hearing care all over the world, Demant is active and engaged. We employ more than 14,000 world-wide and are a growing business in intelligent audio solutions for gaming and office communication is also a significant part of the Group. Our journey has begun, do you want to join?We are a team of three based in the office in Askim, Sweden. We are responsible for ensuring regulatory product compliance. It is our job to ensure product registrations worldwide and provide guidance for quality system compliance during development projects. We follow AIMD, MDD, ISO 13485, and QSR etc. To describe your team in the best way, we believe in a collaborative and open culture. We depend on each other to share know-how’s and challenges because we believe that the best results come from a fruitful team effort. We work interdisciplinary and across countries with our colleagues in Copenhagen and Nice. As part of the product registrations you will also be working closely with our distributors worldwide. Hence, you should expect to travel around 15 days annually. Responsibilities in shortA description of an everyday can be difficult to provide, as we claim that we do not have two days alike. We will try to provide you with an overview of what you will be responsible for. Your main responsibility is to participate in creating worldwide regulatory strategies and provide regulatory input to product launch plans. Furthermore, you will prepare regulatory documentation for product submissions, licence renewals and periodic updates. To do a good job, you need to find it easy to convert and translate technical documentation into the regulatory demands. In your role as a regulatory affairs specialist you also work as a project managerresponsible for coordinating cross-functional activities to enter new markets. As part of your work you will also conduct distributor quality management system audits and support development of relevant SOPs as well as work instructions. What we are looking forYou are passionate about efficiency, structure and regulatory compliance and understand the challenges of working in a fast-growing environment. The basics to perform well:You have at least 1-2 years working with QA/RA, preferably with medical devices. You have at least basic understanding of AIMDD or MDD, ISO 13485, and QSR.As we are a global company, you communicate effortlessly in English and are used to write in English. If you have French or Spanish language proficiency we consider this as meriting. We know you can! We trust and value your professionalism, experience and dedication. Your new perspectives, insights and ideas are the cornerstones of our success, and we encourage you to think out of the box and participate developing our ways of working. Want to see it from our side?To apply for this position please attach your CV and short motivational letter in English not later than June 7, 2019, by using the link “Apply now”.Please note that we only accept applications send through our online web platform. Don’t hesitate to reach outFor more information about the job, please contact Satu Hjärtstam, Head of Regulatory Affairs on +46 735 44 98 13 .If you have questions to the recruitment process please reach out to Ditte Mi Petræus on +45 5381 3547 We are excited to get to know you. About Oticon MedicalOticon Medical is a global company in implantable hearing solutions, dedicated to bringing the magical world of sound to people at every stage of life. We are part of the Demant Group - one of the world’s largest groups of hearing health care companies with more than 14,000 employees worldwide and revenues of over DKK 14 billion. We share a close link with Oticon and have direct access to the latest advancements in hearing research and technologies. Our competencies span more than a century of innovations in sound processing and decades of pioneering experience in hearing implant technology. By working collaboratively with patients, physicians and hearing care professionals, we ensure that every solution we create is designed with user needs in mind. We share an unwavering commitment to provide innovative solutions and support that enhance quality of life for people wherever life may take them. Because we know how much sound matters. Visa mindre

Play a key role as responsible for our change management process

Because people matters! Our mission is clear: We want hearing impaired to be able to experience the sounds of life. This is the foundation for everything we do – which drives us and keeps us focussed on innovation efficacy. We want to develop the world’s best hearing healthcare solutions. Right now, we are looking for a dedicated Documentation Engineer to support our fast-growing business and international expansion. Bone Anchored Hearing SystemsThe job we... Visa mer
Because people matters! Our mission is clear: We want hearing impaired to be able to experience the sounds of life. This is the foundation for everything we do – which drives us and keeps us focussed on innovation efficacy. We want to develop the world’s best hearing healthcare solutions. Right now, we are looking for a dedicated Documentation Engineer to support our fast-growing business and international expansion. Bone Anchored Hearing SystemsThe job we offer you will play an important part of ensuring to keep our products on the market! Team wise, you can look forward to joining the Operations team consisting of 9. The team is responsible for all manufacturing and logistics activities as well as maintenance of all products released to market. Besides your closest colleagues you will be working closely with the other functions in the company and the administration departments of our external partners.United we win. We believe that the best results come from a fruitful team effort. We support each other and constantly share feedback and knowledge to improve our results. We have an informal and creative atmosphere where respect is pivotal and we strive for the common goal. Core responsibilitiesWe would like to offer you a role, where You will have the administrative responsibility for our product change management and an important role in ensuring a well-executed change process.This is a new position created to support a growing organisation, giving the opportunity to influence our internal procedures. You will be situated in our Gothenburg office working with Bone Anchored Hearing Systems (BAHS).You will have a wide variety of responsibility and tasks. Within change administration, you will:Host the Change Management board including invitation, preparation, planning and documentationEnsure that changes to products, printed material or the quality system are reviewed and approved before implementationEnsure that documentation and information related to changes is correctly transferred to internal and external stakeholdersFollow up; ensure implementation of changesEnsure that internal procedures for change management are followed and accurate. (Including performing internal training when needed.)Set up collaboration with critical suppliers regarding change management together with purchaser Within documentation maintenance:Updating documentation connected to released products and procedure e.g creating and updating documentation connected to released products - such as specifications and technical reportsEnsure implementation of new/updated documentation such as drawings and specifications What you can bring into playIf you have:B.Sc. / M.Sc. in Engineering or similar relevant backgroundSome experience with one or more of these categories change management processes, quality assurance, and regulatory affairsIndustry knowledge from medical device or another highly regulated area is merited Since you are having a lot of different interfaces both internally in the organization and externally, you will be successful if you know the value of long-term relationships.Professionally you are driven by implementing improvements. You have a passion for administration and documentation – and who understands the importance of medical device product documentation.On a personal level, your professional style is characterized by your thoroughness and ability to work structured and focused. Besides that, we would like to see that you are pragmatic and strive for efficiency in all that you do.You have a holistic view of thinking and acting and are driven by taking responsibility. We believe in the good lifeWe create solutions that allow people to live their lives to the max! We also recognize that in order to bring energy and inspiration to work, you need to re-energize and spend time with family, friends and hobbies in a healthy work life balance. We offer you professional and personal development opportunities. Want to see it from our side?To apply for this position please attach your CV and personal letter in English but not later than 30 April, 2019.For more information please contact Magdalena Eriksson, +46 (0) 76 1719468.Questions about the recruitment process contact Ditte Mi Petræus +45 53813547. We are looking forward to hearing from you. Visa mindre

Regulatory Affairs Specialist

Developing implantable hearing aids that truly make a difference to hearing impaired is our mission. We are all passionate about ensuring high life quality. This can also become your mission as we are hiring. Our background storyOticon Medical AB is part of Demant Group. Demant is a world-leading hearing healthcare group that offers solutions and services to help people with hearing loss connect and communicate with the world around them. For more than a c... Visa mer
Developing implantable hearing aids that truly make a difference to hearing impaired is our mission. We are all passionate about ensuring high life quality. This can also become your mission as we are hiring. Our background storyOticon Medical AB is part of Demant Group. Demant is a world-leading hearing healthcare group that offers solutions and services to help people with hearing loss connect and communicate with the world around them. For more than a century, the Demant Group has played a vital part in developing innovative technologies and know-how to help improve people’s hearing and health. In every aspect, from hearing devices, hearing implants and diagnostic equipment to hearing care all over the world, Demant is active and engaged. We employ more than 14,000 world-wide and are a growing business in intelligent audio solutions for gaming and office communication is also a significant part of the Group. Our journey has begun, do you want to join?We are a team of three, based in the office in Askim, Sweden. We are responsible for ensuring regulatory product compliance. We are responsible for product registrations worldwide and guidance for quality system compliance during development projects. We follow AIMD, MDD, ISO 13485, and QSR etc. To describe your team in the best way, we believe in a collaborative and open culture. We depend on each other to share know-how’s and challenges because we believe that the best results come from a fruitful team effort. We work interdisciplinary and across countries with our colleagues in Copenhagen and Nice. To ensure sufficient collaboration with the projects you are expected to spend 1-2 days a month in our offices in Denmark and / or France. Responsibilities in shortWe would like to give you a peak into what you might expect to work with, and this might be tricky, as you will see that our days are not the same. You will primarily work with product development projects related to our bone-anchored hearing solution with regulatory focus. You are representing QA/RA in assigned projects and we wish for you to utilize your expertise with providing guidance in quality system compliance as well as regulatory compliance. You need excellent planning skills to establish the regulatory plans on assigned projects. Furthermore, you lead the accomplishment of risk management activities in the projects. You hold the role in securing establishment and regulatory compliance of product documentation and perform product registrations worldwide, either directly or through distributors. A part of your job is also to support development of product labelling and ensure compliance with product claims and achieved product registrations. With the new Medical Device regulation taking affect in May 2020, we need to be well-prepared. We are already implementing the changes in our current product portfolio and for the future. This means that you will also have an important role in supporting the implementation. What we are looking forYou are passionate about efficiency, structure and regulatory compliance and understand the challenges of working in a fast-growing environment. The basics to perform well:You have at least 3 years working with QA/RA, preferably with medical devices. You have a thorough understanding of AIMDD or MDD, ISO 13485, and QSR.As we are a global company, you communicate effortlessly in English and are used to write in English. If you have French or Spanish language proficiency we consider this as meriting. We know you can! We trust and value your professionalism, experience and dedication. Your new perspectives, insights and ideas are the cornerstones of our success, and we encourage you to think out of the box and participate developing our ways of working. Want to see it from our side?To apply for this position please attach your CV and short motivational letter in English not later than June 7, 2019, by using the link “Apply now”.Please note that we only accept applications send through our online web platform. Don’t hesitate to reach outFor more information about the job, please contact Satu Hjärtstam, Head of Regulatory Affairs on +46 735 44 98 13 .If you have questions to the recruitment process please reach out to Ditte Mi Petræus on +45 5381 3547 We are excited to get to know you. About Oticon MedicalOticon Medical is a global company in implantable hearing solutions, dedicated to bringing the magical world of sound to people at every stage of life. We are part of the Demant Group - one of the world’s largest groups of hearing health care companies with more than 14,000 employees worldwide and revenues of over DKK 14 billion. We share a close link with Oticon and have direct access to the latest advancements in hearing research and technologies. Our competencies span more than a century of innovations in sound processing and decades of pioneering experience in hearing implant technology. By working collaboratively with patients, physicians and hearing care professionals, we ensure that every solution we create is designed with user needs in mind. We share an unwavering commitment to provide innovative solutions and support that enhance quality of life for people wherever life may take them. Because we know how much sound matters. Visa mindre

Mechanical Engineer that wants to make a difference in hearing health care

Ansök    Maj 7    OTICON MEDICAL AB    Finmekaniker
Are you ready to make a difference for people with a severe hearing disability, and are you fueled by professional pride and curiosity? Are you skilled within the area of fine mechanics design and do you want to be part of developing new and innovative implantable hearing solutions?Then we can offer you an exciting opportunity as Mechanical Developer at Oticon Medical. At Oticon Medical, we develop both Bone Anchored Hearing Systems (BAHS) and Cochlear Imp... Visa mer
Are you ready to make a difference for people with a severe hearing disability, and are you fueled by professional pride and curiosity? Are you skilled within the area of fine mechanics design and do you want to be part of developing new and innovative implantable hearing solutions?Then we can offer you an exciting opportunity as Mechanical Developer at Oticon Medical. At Oticon Medical, we develop both Bone Anchored Hearing Systems (BAHS) and Cochlear Implants (CI). We are a fast growing and agile company. We are ambitious and possess an entrepreneur spirit and the will to win. We offer an opportunity to join us on our exciting journey and to help us develop innovative implantable hearing solutions that improve the lives of thousands of children and adults across the globe. This job relates to the BAHS products and the role is situated in modern offices in Askim, right outside Gothenburg.Successful in the jobFor you to be successful in this job, we are looking on following skills and qualifications:You are motivated by hands-on mechanical design and product development with a clear focus on customer needs, and by working in cross-professional development teamsYou likely hold a BSc or MSc degree in mechanical engineering.Either a few years’ experience working as developer, design engineer OR a genuine mechanical design interest.Knowledge within Medical device development is an asset.Experienced in CAD modeling, preferably Creo.Well structured and good documentation skills.Fluent in English (spoken/written)A proper work-life balance is a key focus area in our organization and while flexibility goes both ways you are able to travel up to 20 days per year. Responsibilities includeMicro-mechanical design – from requirements and concepts to products running in productionProduct development and design3D CAD modelling – we use PTC CreoDesign, build and test physical prototypesCost and production optimization of designsChange order management support, meaning based on user or production input update designs and specifications for products.Ensuring regulatory compliance of materials, designs and documentation. United we winWe believe that the best results come from a fruitful team effort. As a group, we have a lot of accumulated knowledge and we understand the value of knowledge sharing, which provides an inspiring and creative work environment. We support each other and constantly share feedback and knowledge to improve our results. We have an informal and creative atmosphere where respect is pivotal and we strive for the common goal. As a person you should be a flexible and positive person that thrives from team work. Join our amazing team!We are screening applications continuously, and would like to receive your application not later than June 7, 2019. For questions regarding the position, please contact Erik Holgersson on [email protected] We look forward to hearing from you. Visa mindre