Beschreibung
QA Specialist with profound Database and reporting knowledge wanted for our Fribourg based client in the pharmaceutical sector.Your experience/skills:
- University degree or equivalent education in Life Sciences or a related field
- 2+ years' working experience in quality assurance
- Strong understanding of regulatory requirements and guidelines for drugs and devices
- Background in Database and reporting with MS Office Suite, competent handling of Swissmedic trading requirements is a plus
- Familiarity with ISO 13485 and GxPs
- Languages: fluent English both written and spoken, German or French is advantageous
Your tasks:
- Generating and maintaining company Standard Operating Procedures (SOPs), and Supporting Documents in compliance with external regulatory and legislative requirements
- Conducting the implementation and maintenance of the company specific Quality Manual ensuring the ongoing site compliance
- Identifying and deploying compliance metrics as well as providing training to company associates on core quality system functions, writing procedures and good documentation practices
- Leading internal quality audits to perform the level of compliance and supporting external audits and inspections
- Assisting in Swiss medic inspections and providing reports on a monthly basis to management on the progress of outstanding local corrective and preventative actions
Start: ASAP
Duration: 06MM+
Location: Fribourg, Switzerland
Ref.Nr.: BH13358
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