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Upstream Biotechnology SME
- Permanent
- Bioprocessing
- Iceland
This vacancy has now expired. Please see similar roles below...
Proclinical are recruiting for an Upstream Biotechnology SME to join a biotech organisation. This role is on a permanent basis and is located in Reykjavik.
Responsibilities:
- Exhibit operational excellence in the functional area of responsibilities.
- Evaluate written processes, SOPs, BMRs and any other cGMP documentations within span of knowledge.
- Support the implementation of technical and validation protocols.
- Guarantee the USP suite and equipment is always preserved within a state of inspection promptness.
- Participate in successful commercial pre-approval inspections, routine audits and any other engagements with regulatory agencies when needed.
- Conduct cGMP actions in Grade CNC, D and C areas.
- You will prepare media and buffer to set specifications rendering to written protocols.
- Other duties may be assigned.
Key Skills and Requirements:
- Educated to a degree level in a pertinent field or pertinent work experience.
- Know-how of mammalian cell culture for cGMP production of monoclonal antibodies and recombinant protein therapeutic products.
- Familiarity with operating upstream processing equipment would be ideal.
- Expertise on cell culture principles, practices, scale up, technology transfer and process validation actions.
- Demonstrable experience working within a biopharmaceuticals or technical discipline would be preferable.
- Works well in a team.
If you are having difficulty in applying or if you have any questions, please contact Dominic Williams at +44 203 987 6281.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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