Beschreibung
QA/PV Manager (m/f/d)
Reference: -en
Start: asap
Duration: 10 MM+
Main tasks:
- Ensure GDP/GMP compliance in cross functional collaboration with Regulatory Affairs and Supply Chain
- Perform local national release in accordance to Swiss requirements
- Manage local deviations and manage complaints with the manufacturing site and the global functions
- Manage change requests in accordance with quality agreements
- Qualification of customers and suppliers
- Support Qualified Person in self-inspections, audits and authority inspections
- Adaption and review of local SOPs
- Manage safety information in local PV unit according to appropriate Standards and SOPs.
- Monitor local Risk Management Plans and risk minimization activities
- Support Market Research and/or Patient Support Programs as local PV partner
- Review local medical literature
- Support PV audit/inspection readiness
Main qualifications
- Pharmacist or master's degree in science
- Profound experience in pharmaceutical industry in Quality, Pharmacovigilance or Regulatory Affairs
- Fluent written and spoken German and English / fluent spoken French is an advantage
- Experience with industry standard IT tools (SAP, Trackwise) is an asset
Main advantages:
- A very renowned company
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
My contact person:
Yvonne Hollatz
Referencenumber:
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