Mandated by our client company, we are looking for a R&D Quality Specialist. In this role, you will support the supervisor in the timely release of GMP relevant documents. Support departmental projects and objectives according to agreed timelines and standards in the given area of competency and support adherence to compliance with GMP in TRD. General Information: Workload: 100% / Duration: 18 months max. / Remote work: only sporadically Work location: Basel
R&D Quality Specialist
- 1. Perform review of GMP relevant documents for compliance with SOPs (e.g. review of analytical raw data and analytical documents).
- 2. Clarify simple deficiencies in GMP documents with the line unit experts in own responsibility.
- 3. Recognize complex deficiencies in GMP documents, report them to supervisor, suggest actions and supervise agreed follow-up.
- 4. Write and complete GMP relevant documents in own area of responsibility (e.g CoAs, BRR sheets).
- 6. File and archive documents owned by QA
- 7. Collaborate with other associates to support the service function of QA
- 8. Participate in knowledge exchange in TRD.
- 9. Participate in training of new and temporary employees
- 1.Laboratory technician certification or Bacehelor (chemistry, analytics, biologics) or other university degree with focus on analytics
- 2.Previous Working experience in Quality Assurance or Quality Control in a regulated environment (GMP), preferably in pharmaceutical companies.
- 3. Languages: German and English in written and spoken
- 4. Aptitude for co-operation, good team player
We look forward to receiving your application via the online application form.
Core Recruitment
Elias-Canetti-Strasse 2
Zurich
T: +41 58 307 29 60
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