Quality Officer - Pharmaceutical Production
Oxford Global Resources - Amsterdam
We are looking for a Quality Officer that is responsible for ensuring GMP-compliance on the production floor in this international biotech firm in Amsterdam. You oversee all GMP-documentation from production, and are present - Volledige vacature bekijken
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Production leader biotech
Production leader biotech
LocationLimburg, Netherlands
Business Sector
Biotechnology
Contact email
Job ref
23000
Published
17 days ago
For a big
biotech company
in
Limburg (Netherlands)
we are looking for a
production team
lead with experiences within
biotechnology processes
.
As a production team lead you lead and innovate in the production of cell therapy products, adhering to the highest GMP regulations. Dive into a role where every day is different, surrounded by a team that's as ambitious as it is diverse.
This company is committed to making a meaningful difference in people's lives, achieving our business goals with integrity, and respecting our people and the planet. At our core, we believe in solving complex problems and generating new ideas in life sciences, offering you the satisfaction of contributing to improving lives worldwide.
Key Responsibilities:
Take the helm in managing, performing, and overseeing all cell- and tissue culture activities, ensuring strict compliance with cGMP regulations. Efficiently plan, organize, and coordinate production, maintenance, and cleaning activities within the production areas.Play a crucial role in the qualification and development of the Biotech Associates team (12 FTE), ensuring the seamless handover of information between shifts and maintaining the highest levels of GMP compliance and quality in manufacturing activities.
Hands on team leading role, you will be standing within the team (in the cleanroom), being the bridges between the production manager and the production floor.
Being part of the production process: a high-tech biotechnology process with T cel for the treatment of cancer.
Drive the generation, review, and approval of manufacturing documents in alignment with GMP regulations and in coordination with various departments. Initiate and monitor deviations, CAPA’s, and changes, working closely with the QA department to enhance processes, planning, and training.
Key Requirements:
A BSc/MSc degree in biochemistry, biotechnology or pharma with a focus on cell biology and/or human cell culturing techniques.2+ years of experiences within a team leader role.
Demonstrable expertise in tissue or cell culture within a laboratory/GMP environment.
Exceptional people management skills coupled with the ability to communicate fluently in English.
A knack for planning and organizing, complemented by flexibility, problem-solving capabilities, result orientation, and a meticulous attention to detail.
INTERESTED?
Interviews and offers can happen the coming two weesk!
If you’re interested in the above description, please apply with your CV today. For further information, please contact Jane Tiemessen at +31 (0)20 20 44 502 or by email at j.tiemessen@panda-int.com
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