Lediga jobb som Laboratoriechef i Göteborg

Location: Gothenburg, Sweden
Sector: Biotechnology / NGS / Molecular Diagnostics
Type: Full-time
Role Overview
We are seeking an experienced professional with strong expertise in NGS laboratory operations to support the scaling of our diagnostic services.
In this role, you will work closely with the Laboratory Manager to oversee daily operations, optimize workflows, and ensure the highest standards of quality across our NIPT and genomic services. You will play a key role in bridging technical excellence with operational efficiency in a regulated laboratory environment.
Key Responsibilities
Workflow Coordination: Oversee and coordinate end-to-end laboratory processes, ensuring consistent and efficient execution of NGS workflows.
Process Optimization: Continuously develop and refine laboratory protocols to improve efficiency, reduce turnaround times, and maintain high quality standards.
Technology & Tech Transfer: Support the coordination of technology transfers and implementation of new genomic platforms within the laboratory.
Digital Integration (LIMS): Collaborate on the development and optimization of Laboratory Information Management Systems (LIMS) to support laboratory operations, logistics, and reporting.
Resource Management: Manage laboratory inventory, contribute to resource planning, and support supplier coordination to ensure uninterrupted operations.
Cross-Functional Collaboration: Act as a key liaison between the laboratory and functions such as IT, Logistics, and R&D, working closely with international stakeholders.
Quality & Troubleshooting: Take an active role in troubleshooting technical issues and ensuring all laboratory activities meet regulatory requirements and internal quality standards.



Qualifications & Skills
Education: Advanced degree (M.Sc. or Ph.D.) in Biotechnology, Biochemistry, Molecular Biology, Medicine, or a closely related Life Sciences field.
Experience: Minimum 2 years experience in a senior laboratory role, including direct responsibility for operational oversight in a clinical or diagnostic laboratory setting.
Technical Expertise: Demonstrated hands-on experience with Next-Generation Sequencing (NGS) workflows in a clinical setting, including implementation, validation, and routine operation of NIPT or similar assays. Prior experience with Illumina Veriseq platforms in a production environment, including troubleshooting, optimization, and quality control, is required.
Leadership: Proven ability to lead and develop technical teams, while operating effectively in a matrix or multi-site organization. Comfortable engaging with both laboratory staff and senior management.
Problem-Solving: Strong analytical and troubleshooting skills, with experience resolving complex technical and operational issues in a live production environment.
International Collaboration: Experience working in cross-border or multi-site laboratory environments, with the ability to coordinate across different teams, processes, and regulatory expectations.
Language: Proficiency in English is required. Working knowledge of Croatian, Serbian or Slovenian is highly advantageous due to collaboration across group laboratories. Swedish is beneficial but not required. Visa mindre

We are building a state-of-the-art facility and a world-class team of technologists for R&D into next-generation battery cells, and we are now looking for a Prototype Lab Manager to make it happen. You will play a key role in building up our new MLPC (multi-layer pouch cell) prototype lab and grow your own team of technicians to operate it.

Volvo Cars is one of the most well-known and respected car brands in the world. Northvolt is a leading supplier of sustainable, high-quality battery cells and systems, dedicated to delivering the world’s greenest lithium-ion battery.

Together, we have formed a joint venture, NOVO Energy, to power the next generation of pure electric Volvo and Polestar cars.

What You’ll Do

To start with you will work in close collaboration with the Senior Director of Programs to build up our lab, you will also act as a super user for one of the filed in the lab, electrode, assembly or cycling. A big focus for you will be people management: hiring, scheduling and training. You and your team will execute and analyze cell builds, in close collaboration with R&D Engineering and other internal stakeholders.

You will be responsible for the lab operations, setting up the way of working, handling in-going material needs, implementing laboratory operational requirements to support analysis, all in all ensuring that laboratory operations run safely and efficiently.

Last but not least you will take part in continuous improvement of methodology and technology in order to secure the highest standards of safety, quality, and output.

Your Background

We are looking for an engaged leader, with experience in manufacturing in a regulated industry, preferably battery development/manufacturing. You take ownership and are eager to collaborate to achieve great results. You thrive in a multicultural and fast-changing environment.

You are a highly organized and result-driven individual with an eye for detail and a sense of quality. You have been involved in driving large, innovative, and challenging projects with high demands on accuracy and on-time delivery.

- Several years of experience working in a lab environment, preferably during “set-up” phase
-
A couple of years of leadership experience (project or people management)

-
Experienced with 5S, HSE, test/production planning and standardization

-
English verbal and written communication, and detailed documentation skills




Volvo Cars is one of the most well-known and respected car brands in the world. Northvolt is a leading supplier of sustainable, high-quality battery cells and systems, dedicated to delivering the world’s greenest lithium-ion battery. Together, we have formed a joint venture, NOVO Energy, to power the next generation of pure electric Volvo and Polestar cars.

Our Gigafactory in Gothenburg will be one of the largest cell production facilities in Europe, with a potential annual cell production capacity of up to 50 gigawatt hours (GWh) - thereby enabling a supply of batteries for approximately half a million Volvo and Polestar cars per year. Our state-of-the-art R&D facility will gather leading expertise from all over the world, to create the next generation battery cells.

You can read more about this joint venture in these press releases, here and here. Visa mindre

We are building a state-of-the-art facility and a world-class team of technologists for R&D into next-generation battery cells, and we are now looking for an R&D Lab Manager to make it happen. You will lead the Cell Build Team and coordinate the research-oriented work we perform in our lab facilities. We are a diverse engineering team with a common goal to enable the future of energy.

Volvo Cars is one of the most well-known and respected car brands in the world. Northvolt is a leading supplier of sustainable, high-quality battery cells and systems, dedicated to delivering the world’s greenest lithium-ion battery.

Together, we have formed a joint venture, NOVO Energy, to power the next generation of pure electric Volvo and Polestar cars.

What You’ll Do

You and your team are responsible for the entire cell build process and cycling testing of battery cells. The team execute the battery electrode and process development for advanced high-energy density Li-ion batteries, by building and assessing new electrode material as well as conducting systematic processing experiments. The work is conducted in a lab environment with analytical equipment (XRD, SEM, DEMS, BIT, optical microscope, data logger, thermal sensing devices, voltmeter, oscilloscope, etc.). The team works closely with material, design, and manufacturing teams to ensure the successful development of battery cells.

You will be responsible for setting up the organization and way of working, from the in-going material need to end-of-life testing, implementing laboratory operational requirements to support analysis, all in all ensuring that laboratory operations run safely and efficiently. You will also focus on the people management responsibilities, handling hiring, scheduling, training, and development.

You will work closely with other engineering teams to coordinate cross-functional activities that improve laboratory operations. You will drive continuous improvement of methodology and technology in order to secure the highest standards of safety, quality, and output.

Your Background

We are looking for an enthusiastic R&D Lab Manager with experience in leading activities of lab/test engineers and with the ability to plan around multiple priorities and communicate the status of work activities. You take ownership and are eager to collaborate to achieve great results.

Further, you are a goal-oriented, curious, and persistent person that enjoys solving problems at their root causes and thrives in a multicultural and fast-changing environment.

- BSc or MSc. degree within relevant field of engineering
- Several years of experience in relevant lab positions
- Understanding of lithium-ion cell safety and its risk
- Experience in lab quality control systems
- English verbal and written communication, and detailed documentation skills



Volvo Cars is one of the most well-known and respected car brands in the world. Northvolt is a leading supplier of sustainable, high-quality battery cells and systems, dedicated to delivering the world’s greenest lithium-ion battery. Together, we have formed a joint venture, NOVO Energy, to power the next generation of pure electric Volvo and Polestar cars.

Our Gigafactory in Gothenburg will be one of the largest cell production facilities in Europe, with a potential annual cell production capacity of up to 50 gigawatt hours (GWh) - thereby enabling a supply of batteries for approximately half a million Volvo and Polestar cars per year. Our state-of-the-art R&D facility will gather leading expertise from all over the world, to create the next generation battery cells.

You can read more about this joint venture in these press releases, here and here. Visa mindre

Är du en driven och inspirerande ledare som arbetar nära dina medarbetare? Har du ett affärsmässigt fokus för att tillsammans med dina medarbetare kunna möjliggöra att vår kunskap når ut och tillämpas? Då kan du vara vår nya Enhetschef för Infrastrukturlabb.

Om oss
Vi på avdelningen Infrastruktur och Betongbyggande utför uppdrag och bedriver forskning åt såväl näringsliv som offentliga aktörer. Inom enheten Infrastrukturlabb utför vi provning av produkter och komponenter inom VA-system och fjärrvärmenät. Enheten förfogar över omfattande laborativa resurser och huvudsakligen provas en mängd produkter tillverkade av plast. Målet är att skapa nytta för kunder och samhälle och bidra till ett hållbart samhälle med en ökad konkurrenskraft för Sverige och svenskt näringsliv.

Om rollen
I din roll som Enhetschef på Infrastrukturlabb kommer du leda en enhet bestående av cirka 20 engagerade labbingenjörer. I denna roll kommer du att ha ansvar för att leda och inspirera dina medarbetare, för att uppnå verksamhetens mål och bidra till dess utveckling. Du kommunicerar mål och strategier till personalen och fungerar som den operativa ledaren vad gäller resursfördelning och prioriteringar. En viktig del är också att skapa trygghet att främja ett samarbetsklimat som bygger på öppenhet, respekt och delaktighet utifrån arbetsplatsens värdegrund. Du och din enhet arbetar tätt ihop med systerenheten Infrastruktur-utveckling, där projektledning och utvecklingsresurser samlats för de tjänster som dina medarbetare i Infrastrukturlabb levererar.

Som enhetschef rapporterar du till avdelningschefen och ingår i avdelningens ledningsgrupp. Tjänstgöringsorter är Göteborg och Borås, då enheten har verksamhet på båda orter.

Vem är du?
För att lyckas i rollen ser vi att du är en naturlig ledare och förebild som ingjuter förtroende hos både kunder och medarbetare. Du har en stark tro på att hållbara resultat skapas genom engagerade medarbetare. Du är skicklig på att kommunicera så att förväntningar och budskap tydliggörs och når fram till alla medarbetare. Som enhetschef kommer du att spela en avgörande roll i enhetens framgång och i organisationens övergripande planer. Eftersom enhetens verksamhet är kommersiell krävs ett affärsmässigt arbetssätt med ett tydligt fokus på värdeskapande och kundleverans. I rollen är det också viktigt att du kan hantera ett högt tempo, vara snabbfotad och stresstålig.

Vi tror att du har erfarenhet från industribranschen, gärna inom automation och processtyrning. Kunskap inom LEAN management / flödesoptimering är meriterande, liksom erfarenhet från ackrediterad provning. Verksamheten står inför planerad expansion – vi tror att du därför har vana att omvandla vision till praktik kopplat till modernisering av labb.

Är vi rätt för varandra?
Inom RISE gillar vi olika och vi är övertygade om att mångfald bidrar till en innovativ miljö där vi tillsammans utmanar gränser och utvecklar ny kunskap och kompetens för framtiden. Vi lovar dig inte ett lätt jobb men vi kan lova en spännande resa där vi tillsammans med engagerade och kompetenta kollegor bidrar till en hållbar framtid och till att säkra ett försprång i den globala konkurrensen. Hos oss får du möjlighet att göra skillnad på riktigt. Vill du vara med på resan?
Välkommen till oss och hela Sveriges forskningsinstitut och innovationspartner!

Välkommen med din ansökan!
Är du intresserad och vill veta mer så är du välkommen att kontakta rekryterande chef Tobias Lundvall, 070 - 313 69 28, [email protected] eller Anders Hjörnhede, 070 - 629 30 97, [email protected]. Sista ansökningsdag är den 21 maj 2023. Urval och intervjuer kommer ske löpande. Våra fackliga representanter är: Bertil Svensson, Unionen, 010-516 53 56 och Lazaros Tsantaridis, SACO, 010-516 62 21.

Samtal från externa rekryteringsföretag och säljare undanbedes vänligen då vi lyder under Lagen om offentlig upphandling. Visa mindre

Does your passion for science and technology meet your desire to improve life for patients everywhere? You could be our next teammate.
We at Mölnlycke are part of a world-leading medical solutions company, designing and supplying medical solutions to enhance performance in healthcare – from the hospital to the home. We’re looking for people who want to improve outcomes for healthcare professionals and their patients.
And right now, our R&D Laboratories are entering a new phase. As part of our quest to develop the next generation of wound care products, we’re expanding and are looking for new members for our R&D team.
We are now recruiting for a Manager Physical Testing and Method Development
In this role you will oversee and ensure development, testing and delivery of test data accompanied by relevant statistic input and other findings to projects, platforms and factories within assigned area to secure fact based and informed business decisions.
You will lead, manage and coach your assigned team and ensure effectiveness and efficiency in terms of resource utilization and cost management while securing delivery of agreed milestones

Your responsibilities:
Driving the scientific and performance excellence in assigned area as well as identify, develop, allocate and implement new test technologies. Provides input and guidance regarding testing strategies and new concepts to key stakeholders.
Ensures that tests are executed and that test data are delivered in a timely and efficient fashion to support business objectives.
Ensures high-quality and timely support within product development in order to support business objectives in terms of scientific advice, support and tests within assigned area.
Ensures that new models and methods are developed and delivered in a timely and efficient fashion.
Responsible for that the work of own team is compliant with applicable laws, regulations and agreements according to documented order of delegation regarding EHS.
Ensures that regulatory and quality demands are fulfilled within area of responsibility. Analyses tests and report data in accordance with the quality system.
Actively contributing to and implement the R&D Laboratory & Innovation Support strategy and plan aimed at supporting strategic decision making in terms of how & what Molnlycke should focus its efforts on from a scientific viewpoint.


Key Decisions:
Budget decisions in line with agreed budget.
Resource allocation within assigned area of responsibility.
Decision mandate in accordance to appointed role in Mölnlycke QMS and / or other systems, e.g. PLM and LIMS.
Decisions taken in team as expert in area of responsibility, related to:
Test and research methodology
Content on scientific findings


Qualifications:
Relevant Master degree or equivalent working experience.
Relevant leadership experience from line and/or project management positions.
High level of knowledge in assigned area.
Minimum 8 years' experience from relevant area, whereof 2 years from assigned.
Experience of EHS, quality and regulatory demands in assigned area.
Strong ability to coach and motivate co-workers.
Proven ability to handle complex workflows and diverse stakeholders.
Performance driven with excellent collaboration and communication skills.
Experience from working in a cross disciplinary environment.
Fluent English written and spoken.


Apart from making a world of difference by optimizing and developing products for wound treatment:
The opportunity to help improve patients’ lives globally
You will be part of a dynamic team in a global company
A work environment where you will get space for your ideas and you are encouraged to pursue new challenges
An open, friendly and fair working atmosphere
Attractive career growth perspectives
In a near future, you’ll be joining us at our new HQ in GoCo Health Innovation City, fitted with state-of-the-art laboratory facilities
Extra focus on employee wellbeing – it might be a given, but we take it extra seriously at Mölnlycke. Here are just a few examples of how we’ll take care of you:
We have a flexible work from home policy
Activities organized by our internal health and wellbeing organization Mölnlyckan
the opportunity to join our CSR and volunteer activities for Operation Smile
Mobile IT equipment and an annual bonus in addition to your monthly salary A compensation package with generous benefits, such as company health care, company pension plan, travel expense reimbursement, employee benefits platform on products and services and more


If this sounds like you and you feel you have what it takes to succeed in this role, get in touch today!
www.molnlycke.com/careers

About Mölnlycke


Mölnlycke is a world-leading medical solutions company. We design and supply solutions to enhance performance at every point of care – from the hospital to the home.

We specialise in:
Wound management: including dressings with Safetac® such as Mepitel® and Mepilex®
Preventing pressure ulcers: with Mepilex® Border used prophylactically and devices to help turn and re-position patients
Surgical solutions: including Mölnlycke trays, HiBi® antiseptics and Biogel® surgical gloves Visa mindre

Are you a curious scientific leader seeking a role where your expertise can make an outstanding impact? Join a place built on innovation and creativity. Where different views and perspectives are encouraged and valued. An environment that champions inclusion, and teams that reflect the diversity of the communities that we serve.

We are looking for a Associate Director - Team Lead to join our Compound Management group - a delivery focused team where we collaborate to support projects aiming to impact patients' lives. We are responsible for the quality assurance, processing and timely provision of chemical compounds to AstraZeneca's drug discovery projects. The position will be placed at our vibrant AstraZeneca R&D site in Gothenburg, Sweden.

We belong to Discovery Sciences - our wider function that applies deep technical expertise in specialist technologies to support the delivery of targets and molecules to the early AstraZeneca pipeline.

What you'll do:
This position will give you the opportunity to lead a team of enthusiastic scientists, delivering critical support to projects using automated and digital technologies. Continuous improvement permeates everything we do and you will have opportunities to develop and implement innovative technologies and processes.

Designing, performing and interpreting experiments to investigate process improvements and evaluate new technologies is included in the role. We also rely on you to establish successful and productive relationships with local, global and external scientific colleagues and support services to ensure reliable delivery to projects.

Other responsibilities as Associate Director - Team Lead in Compound Management:

* Lead a team of lab-based scientists to support projects according to agreed needs and priorities.
* Develop and coach staff to deliver against departmental objectives and build a successful team.
* Apply your strengths to make impactful personal contributions to the delivery and productivity of the team.
* Develop the strategic direction of the department, and lead initiatives to deliver the strategic plan, achieve scientific excellence and develop the external reputation of Compound Management.

We strongly believe that everyone contributes with a unique set of competence. Your passion for the personal development of yourself and members of your team, combined with support from colleagues, mentors and managers, will ensure you are set up for success in this role.

Essential for the role:
Compound Management is a highly collaborative group, working to tight delivery schedules, so the ability to be comfortable working at a fast, goal-oriented pace, with a team focused approach is crucial to be successful in the role. Furthermore, you have excellent communication skills and a proactive and delivery focused approach. You are passionate about both your own personal development and the development of your team. We also believe you have:

* A MSc/PhD in a scientific subject area, or equivalent experience.
* Leadership and communication skills and a sincere passion for science, technology and innovation.
* Management of risk using evaluative judgments in complicated or novel situations.
* An understanding of drug discovery.
* A strong customer and delivery focus with ability to build trusted relationships with internal and external scientific colleagues.

Desirable for the role:

* Knowledge and experience of working in a sample management role.
* Experience of complex robotic and automated systems, advanced liquid handling instrumentation and laboratory operating systems.

Why AstraZeneca?
Be encouraged and supported to think creatively in our dynamic environment. Here we are free from fear of failure, free to ask the right questions and make bold decisions.

So, what's next! If this sounds like the place and job for you - apply today!

We look forward to find out more about you - make sure you apply no later than the 1st August, 2022.

Additional information:
Our Gothenburg site: https://www.astrazeneca.com/our-science/gothenburg.html
Life in Gothenburg: https://www.movetogothenburg.com/
Make a move to Global Gothenburg: https://www.youtube.com/watch?v=c-Iqbb4aw38 Visa mindre

Are you a wizard in exploring novel target biology and hold a passion for people and science? Would you like to combine your scientific curiosity with your people, strategic and operational leadership skills? If yes, we have the perfect role for you!

We are looking for a Team Leader/Associate Director to mentor and guide the in vitro Target validation team - Applied Stem Cell Sciences in Translational Genomics, Discovery Sciences, Biopharmaceuticals R&D. You will be based at AstraZeneca´s dynamic R&D site in Gothenburg, Sweden. Leading a great team of motivated stem cell scientists and working alongside disease areas specialists to drive Target Validation projects that will power the development of new medicines for Cardiovascular, Metabolic, Renal and Respiratory diseases.

Using your communication skills, scientific knowledge and expertise in stem cell biology, you will have the opportunity to develop a team responsible for designing and delivering target validation data packages using physiologically relevant cellular models across different disease areas.

Thrive in a place where the brightest and most curious minds seamlessly come together in our inclusive environment.

What you'll do:
With your scientific experience and leadership qualities you'll provide strategic leadership for the Target validation team, retaining an alignment and engagement between the Applied Stem Cell Sciences teams and therapy area functions. Through your leadership and support to the team you will be delivering a portfolio of projects by providing direction to the reporting team, the department's leadership team, senior leaders and key partners.

We also rely on you to;

* Plan, design and analyze data from experiments to generate high quality results to support project decisions and breakthroughs.
* Recruit, retain and develop yourself and your colleagues to continuously improve individual and team contributions.
* Identify and develop external partnerships with industrial and academic partners and leaders in the target validation field.

Essential for the role
This role requires a strong scientific drive together with expertise in stem cell models, proven experience in target discovery and validation and mechanistic biology studies combined with a strong strategic and people leadership profile. You also need:

* Engaging line management experience with clarity of purpose, excellent communication skills and a passion for science, project delivery and personal and team development.
* Ph.D. in Cell Biology or equivalent with +8 years of industry or academia experience.
* Track record on leading mechanistic target biology studies in Cardiovascular, Metabolic, Renal or Respiratory disease areas.
* Demonstrable impact and innovation capacity through strong publication record and external scientific reputation within the stem cell field.
* Experience with using bioinformatics platforms to inform target validation approaches.

We truly believe that everyone contributes with a unique set of competence. Your curiosity and passion for personal development combined with support from colleagues and other leaders, will ensure you maximise your skills, abilities and contribution.

Why AstraZeneca?
Here, you'll be encouraged to grow and progress in your own way, building connections with the people around you and sharing in our sense of belonging. Your life at AstraZeneca is defined by you and guided by us. Ultimately, it's more than a job. We know that our work impacts people with serious conditions, many of whom have no other alternatives. That's what drives us - the potential to impact over one billion patients worldwide.

So, what's next? If you're passionate about the possibilities of science to make a difference, welcome to join us!

We look forward to get to know you. Send your application to us as soon as possible, but no later than the 10th April, 2022.

For more information about the position please contact Hiring Manager, Bilada Bilican at bilada.bilican(at)astrazeneca.com.

Additional information:
Our Gothenburg site: https://www.astrazeneca.com/our-science/gothenburg.html
Relocating to Gothenburg: https://www.astrazeneca.se/om-oss/verksamheten-i-sverige/goteborg/relocate-to-gothenburg.html
About BioPharmaceuticals R&D: https://www.astrazeneca.com/r-d.html Visa mindre

Kretslopp och vatten är till för göteborgarna. Vi ansvarar för att några av Göteborgs viktigaste samhällstjänster fungerar, alla dygnets timmar, hela året runt. Genom arbetet med avfall, vatten och avlopp bidrar Kretslopp och vatten till att skapa ett kretsloppssamhälle och göra det lättare för göteborgarna att leva hållbart. Vår vision är "Vi gör det lätt att leva hållbart" och vårt jobb är viktigt på riktigt.

Idag växer Göteborg som aldrig förr. Vi arbetar med att säkra dricksvattenförsörjningen till den växande staden genom att bland annat bygga och underhålla staden under marken där vi har ett långsiktigt och hållbart perspektiv på minst 100 år framåt i tiden. Vi arbetar även med att se till att det avfall som staden genererar samlas in och behandlas på rätt sätt. Vi påverkar och planerar för byggandet av ett Göteborg som ska klara morgondagens klimatutmaningar. Exempel på detta är vårt arbete med hanteringen av skyfall och dagvatten men även arbetet med att påverka göteborgarens medvetenhet och beteende kring avfall.

Vi är en taxefinansierad förvaltning med stor fackkunskap med cirka 500 anställda. Inom organisationen har vi kompetens för att lösa vårt uppdrag - både när vi planerar och utför arbetet. Under våren 2020 har vi flyttat in i nybyggda lokaler vid Alelyckans vattenverk. Här kommer vi vidareutveckla staden för framtiden och våra samarbeten med andra aktörer under många år framöver.

Delar du vår vision och vill veta mer om oss? Besök gärna vår hemsida www.goteborg.se/kretsloppochvatten och följ oss på Facebook eller Linkedin.

ARBETSUPPGIFTER
Avdelningen Dricksvattenproduktion svarar för dricksvattenberedningen i Göteborgs stad på de två vattenverken Alelyckan och Lackarebäck. På avdelningen som består av fem enheter arbetar ca 75 personer.

Laboratorieverksamheten, som omfattar ett större laboratorium på Lackarebäcks vattenverk och ett mindre driftlab på Alelyckans vattenverk, har en mycket viktig roll i arbetet att producera ett hälsosamt och gott dricksvatten. Lackarebäcks laboratorium är ackrediterat mot ISO 17025 och omfattar bland annat våtkemiska analyser, analyser såsom GCMS/ICP-MS, samt mikrobiologi och provtagning. Laboratorieenheten svarar för kvalitetsuppföljningen från råvatten till tappkran, bistår driftenheterna på vattenverken samt ledningsnätet i vattenkvalitetsfrågor, sammanställer och följer upp kvalitetsdata och driver och deltar i utvecklingsprojekt. Laboratoriet styrs till stor del av driftens behov och behöver snabbt planera om i samband med händelser. På båda vattenverken har större utbyggnader genomförts under senare år med nya beredningssteg som ultrafilter och UV-ljus. Laboratoriet har haft en viktig roll i utformningen av dessa nya anläggningar för att möjliggöra en god uppföljning av vattenkvaliteten. På enheten arbetar ca 20 personer.

Samverkan med och stöd till driften i vattenkvalitetsfrågor är en viktig del i det löpande arbetet, vilket kan vara en skillnad mot mer traditionell laboratorieverksamhet. Det handlar bland annat om att snabbt kunna upptäcka och analysera kvalitetsavvikelser, utveckla hjälpmedel och anpassa analysutbudet med utgångspunkt från på driftverksamhetens behov. För att driva ett sådant arbete måste enhetschefen säkerställa att laboratoriepersonalen är väl insatt i vattenverkens beredningsprocesser.
Som enhetschef är du direkt underställd avdelningschefen och ansvarar för den dagliga driften på enheten, personal och ekonomifrågor. Du kommer att ha ett stort kontaktnät såväl inom som utanför den egna enheten.

KVALIFIKATIONER
I rollen ser vi ditt ledarskap som nyckel till framgång. Du fångar det bästa hos varje medarbetare och tar tillvara på allas kompetens. I ditt team arbetar du tillsammans med specialister inom området, där din roll är att lyssna, förstå sammanhang, visa vägen och fatta beslut. Vi söker dig som har högskoleutbildning inom kemi eller mikrobiologi eller motsvarande. Du har erfarenhet av att leda personal och vi tror att du tidigare har arbetat i en ledande befattning inom kvalitetsstyrd laboratorieverksamhet. Erfarenhet av arbete på laboratorium inom en driftorganisation, speciellt inom dricksvattenområdet är meriterande.

Som person har du en tydlig och god kommunikation som uppmuntrar till goda prestationer och tillför entusiasm och energi till dina team. Du själv motiveras av tydligt definierade mål och har förmåga att omvandla dessa till en konkret handling. Du har en förmåga att förena operativa planer med organisationens mål genom din helhetssyn.

Uppföljning och utvärdering av resultat faller dig naturligt. Lika så att analysera situationer och använda den analysen till att metodiskt planera framåt och omprioritera ditt och din enhets arbete utifrån förändrade förutsättningar.

För att bli framgångsrik i rollen som enhetschef ser vi att du motiverar andra och ger råd, stöd och möjligheter till utveckling till dina medarbetare. Du har förmåga att fördela, delegera och kommunicera konkreta delmål för att leda gruppen i den satta riktningen.

Tjänsten är säkerhetsklassad nivå 2 och förutsätter godkänd registerkontroll från Säpo och svenskt medborgarskap. Tjänsten kräver B-körkort.

ÖVRIGT
Välkommen med din intresseanmälan via länken så snart som möjligt, dock senast den 27 maj. Du skickar in din ansökan på randstad.se med CV och personligt brev eller enkelt med din LinkedIn-profil. Tänk på att din LinkedIn-profil behöver vara uppdaterad innan ansökan görs med relevant information.

Inledande intervjuer med Randstad är planerade att hållas under vecka 21/22.
I denna rekrytering samarbetar vi med Randstad. För frågor om rekryteringsprocessen, kontakta gärna rekryteringskonsult Victoria Reeve [email protected] Visa mindre

Would you like to use your clinical project management experience to help deliver life changing medicines to patients? If you would please read on!
At AstraZeneca Be empowered to be innovative and creative where difference is valued. Join a place built on innovation and creativity. Where different views and perspectives are welcomed and valued. An environment that champions inclusion, and teams that reflect the diversity of the communities that we serve.

We’re currently looking for Clinical Sample Project Managers (Compound Leads) to join a dynamic Biosamples team based in either Cambridge (Melbourn Science Park), UK, Gothenburg, Sweden, Warsaw, Poland or San Francisco, US.

Om tjänsten
In this role, you will project manage the delivery of laboratory related activities in both early and late phase global development projects. We’ll look to you to work independently with the clinical project teams and our global external laboratory partners / alliances to ensure operational delivery of the clinical laboratory testing of biological samples, the efficient deployment of tests (including biomarkers, central safety and clinical bioanalysis), as well as data generation and delivery throughout the project lifecycle.

This is a fantastic opportunity to progress your career in clinical development and to play a key role in the development of an exciting portfolio of medicines that will change the lives of patients worldwide.


Dina arbetsuppgifter i huvudsak
Your position will be varied and include the responsibility for ensuring the delivery of all laboratory activities through external partners, meet internal and external quality and regulatory standards all whilst using your operational expertise to advise clinical teams on operational lab strategy, development and deployment. You will regularly be involved in providing advice to clinical teams on laboratory related documentation, operational design and new ways of working, as well as managing external providers to oversee the delivery of relevant lab services and data.

Vem är du?
We are looking for a candidate that have experience in some or all of the following;
• Experience of contributing to the operational deployment of clinical laboratory testing on global clinical development projects.
• Project Management skills to provide operational expertise and guidance to the multiple internal and external parties involved in a clinical project, and a proven record in overseeing external partners, especially multidisciplinary clinical laboratory service providers.
• Influencing skills and experience of negotiations
• A solid knowledge of early or late stage clinical development, as well as an understanding of GCP and GCLP.
Suitable candidates may have a science background and would like to extend their knowledge to clinical study operations (degree educated preferable, but not essential) or have backgrounds including laboratory project management, investigator site coordination or study operations.

In addition to this, the following experiences are also desirable;
• Experience of working collaboratively with external vendors in partnerships or alliances.
• Experience of working in more than one company or country multi-nationally.
• Hands-on experience in a clinical laboratory setting or clinical research site.
• Project management experience.


Om verksamheten
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status or any other characteristic protected by law.

This is a consulting assignment at AstraZeneca during 12 months’ time and with possibilities of extension. During the period of assignment, you will be employed by Poolia. Start date as soon as possible.

Please send your application today or share with your friends.

If you have any questions or comments, please don't hesitate to contact me. Visa mindre

Production Manager Cell Culture Media Production

Company

Takara Bio Europe AB, formerly Cellartis AB, is focusing on stem cell-derived products and services for cell therapy/regenerative medicine, drug discovery and disease modelling. The company leverages long-standing experience in stem cell handling and scale-up together with leading expertise in differentiation of cells into mature and functional human cells. Specifically, the company possesses broad expertise in human pluripotent stem cells, including both hiPSC and hESC and related media. Takara Bio Europe AB is located in state-of-the-art facilities in Göteborg, Sweden and has a newly-established GMP laboratory for production of pluripotent stem cell lines. For more information, visit our website: www.takarabio.com (http://www.takarabio.com)

The company is now looking for the following competence.

Duties & Responsibilities

- Implementation of production of cell culture media
- Lead and manage a small team for the implementation work, and later, the production work of cell culture media
- Maintains broad knowledge of Quality principles and theories including ISO 9001/2015.
- Receive assignments in the form of objectives and determines how to use resources to meet deadlines.
- Work closely with the other stakeholders within the company to foresee requirements and proactively put in place relationships with innovative and compliant laboratory service suppliers
- Work on weekends on a monthly basis
- Other required duties may be assigned.


Education, Qualifications, Skills and Experience

- Minimum MSc in Cell Biology, Microbiology, Engineering or related field.
- Minimum of 5 years of relevant experience preferably in the biotech/biologics ar






More information

For more information about the position, please contact Catharina Brandsten at [email protected].

Please submit your application via this link, no later than January 31, 2020.

We are looking forward to your application. Visa mindre