For our client we are looking for a
QA MANAGER (M/F/D) 100%
The IMP Quality Operations Unit Switzerland in Global Technical Operations is the Quality partner for all Manufacturing Units and Clinical Packaging in Pharmaceutical Technical Development in Switzerland and responsible for the Quality, Quality Systems and GMP-compliance oversight of all Investigational Medicinal Products (IMPs) manufactured and packed for clinical studies in Switzerland.
The Clinical Supply Centre in Basel for Parenterals is responsible for manufacturing Sterile Drug Products for clinical studies. In the course of the implementation of Volume 4 EU Guidelines for GMP Annex 1 (C(2022) 5938, 22-Aug-2022) (and and PIC/S PE 009-16 GMP Guide, Annex 1), the candidate supports and drives end to end the full implementation of Annex 1 in the role as Quality Assurance Manager. The candidate collaborates in close partnership with all involved parties from the Clinical Supply Centre Parenterals.
The candidate supports and oversees the end to end cGMP activities in implementation of Annex 1 requirements at the Clinical Supply Centre Basel. They take care that the Right to Operate can be maintained by ensuring that quality and compliance requirements according to Health Authority expectations and Company Standards for IMP products are given after the successful implementation of Annex 1.
The perfect candidate has sound Quality Assurance knowledge and experience in the area of Annex 1 implementation, sterile Drug Product Manufacturing, Qualification and Validation as well as parenteral manufacturing activities.
Tasks & Responsibilities:
Must Haves:
General Information:
Your Application:
Please apply online. For further information about the position, please contact your Gi Group Recruiter, Fatbardha Igrishta (fatbardha.igrishta[a]gigroup.com).
Branche: Pharma-Industrie
Funktion: Qualitätsprüfung
Führungsperson: Nein
Anstellungsart: Temporäre Arbeit
Karrierestufe: Angestellte/r
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Gi GroupVia Cantonale 2B
6928 Manno
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