Description
QA Compliance Specialist- NOVJP (m/f)
Reference: -en
Start: asap
Duration: 12 MM++
Main tasks:
- Support project activities as member of QA Compliance for activities related to qualification / validation of equipment, utilities and facilities and associated change controls activities
- Review and approve Process Validation Protocols and Reports (Revalidation, Verification, Product Transfers) including associated Risk Assessments and Deviations
- Review and approve Cleaning Validation Protocols and Reports
- Review and approve Equipment, Facility and Utilities Qualification Protocols, Reports
- Perform Quality risk assessments in case of critical deviations and initiate escalation process if applicable
- Support project activities
- Write and review SOPs, forms and report associated
- Provide support for creation, maintenance and retirement of GMP related documentation
Main qualifications
- University or academic degree in Engineering, Chemistry, Pharmacy, Biology or equivalent
- Fluency in German and English
- Experience in QA / QC, Engineering and Production
- Good GMP knowledge
- Experience in the pharmaceutical industry
Main advantages:
- A very renowned company
- You will work in an international environment
- A city with a high quality of life that perfectly embraces both modern and traditional values
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.
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