QA Validation Specialist (m/f/d)
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Switzerland |
Temporary Employment
Job title: QA Validation Specialist (m/f/d)
Industry: BiotechSkills: Anlagenqualifizierung,Qualitätssicherung
Start of project: 01.04.2022
Duration of the project : 6 months
Project volume: 1008 Hours
Location: Switzerland
Tasks:
Consistent implementation and maintenance of the Continued Process Verification (CPV) and Product Quality Review (PQR) programs at Visp
Training and support of the validation teams with the preparation of the CPV/PQR reports, to ensure harmonization and compliance
Preparation of CPV/PQR documents according
Reviewing and approving final CPV and PQR documents
Qualifications:
Bachelor degree in chemistry or related scientific field
Ability to work accordingly to good science
Proficiency in writing scientific reports in English
First experience in GMP compliance is preferred
Experience with statistics or statistical background would be an advantage
Professional English language skills necessary
Referenznummer:
Branche:
Beginn des Projekts:
Dauer:
Anstellungsart:
Kontakt
Patricia Rosas Paredes
P.Rosas-Paredes@aristo-group.ch
+41 44 274 39 00
11022
Biotech
01.04.2022
6 months
Temporary Employment
