Description
The Challenge- Working closely with Production Supervisors to perform investigations into deviations from production
- Writing detailed reports into the deviations and CAPAs according to agreed client templates
- Completing a backlog of deviation investigations to challenging deadlines
Experience
- 5 + years experience working in Quality Assurance within a GMP Pharmaceutical environment handling deviations and ultimately CAPAs
- 2 + years QA experience in an aseptic production environment processes
- Fluent English is essential for this role although Italian would be an advantageThis is a Contract position for an initial 6 months with strong likelihood of extension depending upon performance paying an Hourly Rate depending upon experience. Please contact Deniz Becker at Real Life Sciences by either contacting me directly on the phone number provided or submitting your CV via the link and you will be contacted shortly.
- Next Steps
This is a Contract position for an initial 6 months with strong likelihood of extension depending upon performance paying an Hourly Rate depending upon experience.
Next Steps
Please contact Deniz Becker at Real Life Sciences by either contacting me directly on the phone number provided or submitting your CV via the link and you will be contacted shortly.
Mehr Informationen über Real Staffing erhalten Sie unter www.realstaffing.com/de