Description
CSV Expert wanted for our Basel based client in the pharmaceutical sector.Your experience/skills:
- Master Degree in engineering, IT or science
- 5+ years working experience in pharmaceutical environment, especially with Computer System Validation
- Excellent Project Management skills as well as excellent analytical and problem solving skills
- Strong background in MHRA & FDA requirements and solid knowledge of GxP systems
- Languages: fluent English both written and spoken. German knowledge is a big plus
Your tasks:
- Reviewing and approving deliverables related to CSV in a GMP laboratory environment
- Executing QA reviews and approvals of IT SOPs as well as functional requirements for new and existing computer systems
- Taking responsibility for QA reviews and approvals of all validation related documentation, especially IQ, OQ, PQ, User Requirements, Plan and Traceability Matrix
- Ensuring good and close working relationship with important project stakeholders and internal customers
Start: ASAP
Duration: 3MM+
Location: Basel, Switzerland
Ref.Nr.: BH11641
Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.
Due to work permit restrictions we can unfortunately only consider applications from EU or Swiss citizens as well as current work-permit holders for Switzerland.
Going the extra mile…
New to Switzerland? In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more