Description
We are looking for a
QA/QC Specialist (Techn. Research Development) (m/f)
Reference: -en
Start: asap
Duration: 12 MM
Place: in Basel
Branch: Herstellung von pharmazeutischen Spezialitäten und sonstigen pharmazeutischen Erzeugnissen
Your tasks:
- Manage portfolio of projects, support a discipline and/or provide a service - if applicable, may provide functional expertise in area of responsibility
- Review and recommend disposition of deliverables (e.g. procedures, records, third party work, contractors, clinical trial material, components) to ensure GMP compliance
- QA and QC of primary and secondary packaging
- Perform inspections and audits as required
- Write GMP relevant documents in own area of responsibility (e.g. SOPs with global applicability)
- Meet internal and external guidelines regarding quality and safety (quality manuals, regulatory cGMP guidelines, health authority guidance, SOPs, HSE etc.)
Your qualifications
- Bachelor or Master degree in Sciences or relevant discipline
- Good knowledge of English (oral and written) required; fluency in another language (German)
- Good ability to analyse and evaluate GMP compliance
- Sound scientific, technical and regulatory knowledge in a specific area
- Very good knowledge of cGMPs, working knowledge of safety and environmental regulations and guidelines
- Good knowledge of drug development
Skills:
- Quality management employee
Keywords: Mitarbeiter Qualitätsmanagement