Description
We are looking for a
QA/QC Specialist (m/f)
Reference: -en
Start: 11/16
Duration: 4 MM+
Place: in Basel region
Branch: Herstellung von pharmazeutischen Spezialitäten und sonstigen pharmazeutischen Erzeugnissen
Your tasks:
- 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
- Perform review of GMP relevant documents for compliance with SOPs across several customer groups
- Recognize complex deficiencies in GMP documents, report them to supervisor, suggest actions and supervise agreed follow-up
- Write and complete GMP relevant documents in own area of responsibility
Your qualifications
- Basic degree in laboratory, manufacturing or relevant discipline
- Fluent in site language, English required (adequate knowledge oral & written)
- A solid experience in a corresponding line unit function (e.g. laboratory, manufacture, packaging, IT, documentation)
- Communication skills to sufficiently address GMP and logistic related questions with the line unit experts, in order to maintain GMP records in a compliant status
- Scientific, technical and regulatory knowledge in a specific area
- Basic knowledge of drug development
- Ability to analyze and evaluate GMP compliance
Skills:
- Quality manager