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QA and Regulatory Consultant
Eingestellt von ProClinical aus München
Gesuchte Skills: ISO 13485, GMP, FDA, CAPA, PAL
Projektbeschreibung
This major top-10 Pharmaceutical / Devices Company works in developing innovative medical devices, biopharmaceutical medicines, vetinary products and orthopaedic products. This is a long-term contract (up to 8 months) and the main purpose of the role is performing remediation activities generated from the Management Review Legacy Reviews to ensure adequate product and process risk review.
Skills required:
Expert knowledge of the FDA QSR and ISO 13485/ ISO 9001
Able to review CAPA and sub-system data
Expertise within GMPs
Working knowledge of PAL
Ability to build partnerships internally and externally
Fluent in German and English
Interview process: Telephone interview only
Urgent position
To apply, call or send your CV to Laura Brum, Recruitment Consultant – RA / QA
[email protected]
+49 (0)89 12089 5008
+44 (0)207 44 00 638
Skills required:
Expert knowledge of the FDA QSR and ISO 13485/ ISO 9001
Able to review CAPA and sub-system data
Expertise within GMPs
Working knowledge of PAL
Ability to build partnerships internally and externally
Fluent in German and English
Interview process: Telephone interview only
Urgent position
To apply, call or send your CV to Laura Brum, Recruitment Consultant – RA / QA
[email protected]
+49 (0)89 12089 5008
+44 (0)207 44 00 638
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges