*QC Scientist

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Are you passionate about qualification and coordination? Do you want to be part of building a brand new factory with state of the art laboratories? Join a dynamic and international company that produces new biological medicines and where everyone is responsible for delivering right on time as one team!

We are looking for a QC Scientist with flair for qualification to keep an overview when we move into our new production facility in Søborg.

About the department

With reference to the head of QC Equipment & Planning, you will join QC consisting of 5 departments and 160 dedicated colleagues. The departments are Microbiology, Bioassay, Chemistry, Operations, and Equipment & Planning. We are responsible for method validations for early and late stage products, release analysis of clinical batches as well as commercial and not least analysis of raw materials and stability programs. We are working in an international and customer oriented way to secure fast and reliable manufacturing of medicines to our customers.

The job

To succeed in the job, you thrive in a fast-paced environment. You have a strong desire to create structure and maintain a cool overview while ensuring excellent stakeholder relations. You naturally create a positive and inspiring environment around you and lead by being the good example. You focus on qualification and align both internally and externally. You optimize existing QC processes, incl. drive development of documentation and training for your colleagues.

The main responsibilities are

  • Keep overview of QC qualifications when we move into our new production facility in Søborg.
  • Drive and maintain project plans for equipment qualification and installation
  • Optimize existing QC processes, incl. drive development of documentation and training
  • Report on QC part of project progress to project steering group and leadership stakeholders

As a QC Scientist/QC Coordinator with flair for qualification and coordination you;

  • Work in close collaboration with skilled QC colleagues to ensure project progress.
  • Partner with Project Lead counterparts from Manufacturing, Engineering and Supply Chain Management to ensure alignment towards qualification.
  • Ensure ongoing improvements in our processes and internal procedures.
  • Act as cross-organizational collaborator and facilitator who is willing to drive change.
  • Keep the bigger picture in mind at all times, yet you understand the importance of minding the details.

The ideal candidate is expected to have:

  • A degree in natural science or engineering.
  • Solid IT skills
  • 3+ years of experience in qualification of QC instrumentation
  • Advanced English oral and written communications skills; ability to communicate with management, peers and subordinates effectively, including giving presentations.

Travel activities up to 10 days per year is possible.

AGC offers
AGC Biologics offers a dynamic working place and an excellent opportunity for working and growing with a varied array of tasks and challenges. You will get insight into and experience with the way the various departments throughout a biologics contract development and manufacturing organization interact in order to achieve success. AGC Biologics offers an informal working environment, where humor is part of the daily work life. We respect each other and our individual differences. AGC employees have a flexible attitude and we help each other to reach deadlines together as one team, in accordance with our slogan - Right. On Time.

Application
Submit your application as soon as possible. We treat the applications as we receive then, and conduct interviews with qualified candidates. When the right candidates are found, the add will close.

For further information regarding the position, please contact Stella Brudin, Senior Manager QC Equipment & Planning, at +45 2760 2473

About AGC Biologics
AGC Biologics (AGC) is a global Contract Development and Manufacturing Organization (CDMO) with biomanufacturing facilities in Europe, Japan and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services. AGC Biologics also offers non-exclusive license to CHEF1™, a proprietary CHO cell line development platform. CHEF1 delivers stable, high-titer, production-quality cell lines in optimized time frames. It is the foundation of CMC Biologics’ innovative approach to cell line and process development.

Want to keep posted about our growth and to learn more about our company?

We also urge you to follow us on our LinkedIn Company Page and give us a quick Like on Facebook !

AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.

Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing.


Information og data

Denne ledige stilling har jobtypen "Forsker", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i København

Jobbet er oprettet på vores service den 8.12.2022, men kan have været deaktiveret og genaktiveret igen.

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Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Forsker
  • København
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