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Sr. QA GCP Manager
Eingestellt von Real Staffing Group aus Frankfurt am Main
Projektbeschreibung
* Minimum of 8 to 10+ years' experience in the pharmaceutical/biotechnology industry
* Minimum of 7+ years' auditing in one of the following areas: GCP, GLP, GPvP
* Expert knowledge of technical concepts required for all aspects of GCP Auditing, to include all types of GCP audits; e.g., Study Sites, Vendors, essential study documentation
* Solid understanding of domestic and international pharmaceutical/Biotechnology auditing standards
* Extensive experience supporting regulatory authority inspections of clinical research activities
* Hands-on experience managing quality and compliance projects and programs
* Proven ability in driving quality process improvement initiatives.
* Extensive leadership experience and mentoring skills Thorough knowledge and application of international requirements of Good Clinical Practice (GCP) and ICH Guidelines
To find out more about Real please visit www.realstaffing.com
Projektdetails
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Einsatzort:
San Jose, California, Vereinigte Staaten
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
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Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
Sonstiges