Beschreibung
QA Compliance Specialist wanted for our Stein based client in the pharmaceutical sector.Your experience/skills:
- Academic degree in Engineering, Chemistry, Pharmacy, Biology or equivalent
- 5+ years' professional experience in the pharmaceutical industry in QA, QC, Engineering or Production
- Advanced knowledge of GMP coupled with prior experience with sterile, biotechnology or comparable in other industries, are beneficial
- Excellent know-how of Office tools like Word, Excel and SharePoint
- Languages: fluent English and German both written and spoken
Your tasks:
- Supporting project activities as member of QA Compliance for activities related to qualification and validation of equipment, utilities, facilities and associated change controls activities
- Performing quality risk assessments in case of critical deviations and initiate escalation processes
- Reviewing and approving Process and Cleaning Validation Protocols and Reports including associated Risk Assessments and Deviations
- Writing, reviewing and approving SOPs, forms and reports associated with above duties and providing support for creation, maintenance and retirement of GMP related documentation
- Preparing training modules for QA Compliance and other related themes
- Reviewing and approving Equipment, Facility and Utilities Qualification Protocols, Reports and associated documents including Risk Assessments and Deviations
Start: ASAP
Duration: 12MM+
Location: Stein, Switzerland
Ref.Nr.: BH13818
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