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Gem
Convatec

Test & Reliability Engineer - Sustaining Engineering, Medical Devices

Lejre

Do you have a keen eye for Physical Testing, Product Quality, Reliability, Validation, and Documentation? Are you looking for an opportunity to merge your passion with our expertise in the Test and Verification of Infusion Care Medical Devices, for the treatment of chronic diseases such as Diabetes and Parkinson’s Disease?

As a Test Engineer, you will be involved in developing and working with a diversity of physical test methods. Planning and coordinating tests in our laboratory in Osted near Roskilde, and partners within Global Convatec and external. Most of your time, you will be part of a project team in SEG.

Convatec
Gem
Orifarm

Specialist, Regulatory Affairs (Temporary Position)

Odense S and Søborg

As Regulatory Affairs Specialist, you will be responsible for lifecycle management of products manufactured at Orifarm’s own manufacturing sites. Therefore, you will collaborate closely with colleagues across functions, such as chemists, formulation specialists and co-workers within Quality, Supply Chain, Manufacturing and Sales.

Further, your main responsibilities include to:

  • Gather information and documentation for variation applications
  • Update dossier sections
Orifarm
Gem
Cbio A/S

Scientist (maternity leave temp), cell-based immunotherapies

Søborg

Are you enthusiastic about developing next generation cell-based immunotherapies that bring new hope to late-stage cancer patients?

You will help the R&D team in a 6-months temporary position as one of our coworkers is on maternity leave, and will help the team with a possibility for further extension.

We are looking for a person experienced in immune oncology or related area with documented practical experience in cell culture and flow cytometry.

Pharmacosmos A/S

QA Specialist

Holbæk

We are seeking a competent new colleague to join our QA team in a dynamic and growing company.

You will be part of our highly dedicated team consisting of 5 colleagues working with a broad range of QA tasks such as batch review, processing of complaints, deviations and change requests as well as validation and ad hoc projects.

Pharmacosmos A/S
QV-Compliance A/S

Ingeniør til validering

Roskilde

Vi har brug for en konsulent til et spændende job indenfor kvalificering og validering. Stillingen byder på mange forskellige opgaver og projekter hos vores kunder på det meste af Sjælland, og du får en spændende, travl og varierende hverdag.

Du vil bl.a. koordinere, planlægge og udføre validerings- og kvalificeringsprojekter, som kan omhandle: rengøringsvalidering, sterilisationsprocesser, procesanlæg, IT-validering, klimafaciliteter, produktions-, måle- og laboratorieudstyr.

QV-Compliance A/S
River Stone Biotech ApS

Analytical Chemist – 12 months position

København Ø

We seek a highly motivated ANALYTICAL CHEMISTRY scientist, engineer, or technician for our research laboratory in Copenhagen.

The position will give intellectual challenge and rich possibilities to develop your skill sets as well as being part of commercially and scientifically exciting projects.

You will contribute to the development and maintenance of River Stone’s analysis platform, method development as well as routine sample analysis. You will be part of an enthusiastic and strong analytical chemistry team.

Gem
Novonesis

Senior LIMS Specialist for Global QC Development

Avedøre

In this role you’ll make an impact by working as a Senior LIMS Specialist in our team, where you will take part in management of projects for LIMS changes across QC laboratories and other stakeholders including implementation, documentation and communication.

Future projects could be introducing and validating LIMS solutions on new equipment or technologies, new LIMS functionalities, improving and aligning existing processes.

Novonesis
Ferrosan Medical Devices A/S

Senior Process Specialist

Søborg

Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.

You will become a process owner of one or more of our production processes in SFI. This means that you will be responsible for, among other things, validation documentation, revalidations, and risk assessments for the specific process.

Ferrosan Medical Devices A/S

Process Specialist

Søborg

Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.

Together with the rest of the team, you will be responsible for the daily support of our production lines. You will learn our processes in detail and gain a good overview of the documentation used in production.

Radiometer Medical ApS

Senior QA Specialist

Brønshøj

The Senior QA Specialist for Radiometer is responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms. This is done by cooperating, supporting, facilitating, training, and communicating towards the best results with partners in R&D.

This position is part of the QA Design Control department, hybrid based and located in Brønshøj. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses.

Biomar, Brande

Aqua feed process technology - Innovation Scientist/Engineer

Brande

Do you have an interest in innovative process technology projects where you are part of developing the next generation of fish feed, looking into functional feed/food ingredients and technologies?

The position will focus on development of new feed types and applications, ingredient science and process technology knowledge.

You will join a great company with engaged colleagues and strong focus on innovation, furthermore health insurance, lunch arrangement at site, salary and other employee benefits which matches the market.

Biomar, Brande
DTU, Danmarks Tekniske Universitet

Postdoc in Biotechnology – DTU Chemical Engineering

Kgs. Lyngby

Department of Chemical and Biochemical Engineering invites applications for a position as Post Doctoral Fellow to be hired within the frame of a project on biogas conversion to single cell protein in the form of methylotrophic bacteria, where optimising synergistic microbial interactions is a key element.

Project focus is on recovery of nutrients from the biogas digestate by microbial or electrochemical methods.

Gem
BESTSELLER

Senior Environmental Impact Specialist

København K

Are you passionate about making a difference in the apparel and textiles industry by measuring and communicating environmental impacts?

As a Senior Environmental Impact Specialist you act as the internal go-to specialist and it is expected that you engage with various stakeholders internally and externally to provide specialised knowledge.

Ferring Pharmaceuticals A/S

Senior Technical Writer - Regulatory (CMC)

Kastrup

You will join the Technical Writing team within Global Regulatory Affairs. We are responsible for global regulatory CMC writing of regulatory documents in applications for new approvals, worldwide market expansions, and product lifecycle activities. We work with a variety of pharmaceutical products, including small molecules, peptides, biologicals, recombinant products, and gene therapy.

Stepping into an informal and collaborative environment, you will have close interfaces with many different disciplines, including Global Pharmaceutical R&D, manufacturing sites, Product Supply, Quality Assurance, Ferring affiliates, and development sites around the world.

Ferring Pharmaceuticals A/S
Gem
Orifarm

Manufacturing Science & Technology (MS&T) Technical Transfer Project Manager (Sr Specialist)

Odense S

Join Orifarm and take charge of building strong business relationships with a key portfolio of our suppliers!

As a MS&T Technical Transfer Project Manager, you will be responsible for securing technical support to Supplier Relationship Management functions, and manufacturing sites comprising support, technological transfers between CMOs and own manufacturing sites, analytical method development and validation, external product development at CDMOs and driving continuous technological improvement and innovation.

Orifarm

Senior Research Scientist

Måløv

Would you like to be part of a team that plays a significant role in the innovative pipeline of creating new medications through the implementation of advanced technologies?

Special Consultant, Mass Spectrometry

København N

The Proteomics Program aims to ensure that Novo Nordisk Foundation Center for Protein Research (CPR) retains world-leading mass...

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Environmental Supporter

Kalundborg

Do you have a flair for natural science and an interest in environmental support of aseptic production?

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