Mein Arbeitgeber
- IMP Quality Operations Switzerland is responsible for delivering Investigational Medicinal Products (“IMPs”) to patients in compliance with cGMP. They are the Quality Partner for all Manufacturing Units and Clinical Packaging in Pharmaceutical Technical Development in Switzerland and responsible for the Quality and Compliance oversight of all
- Acts as a delegate of the Swiss RP for IMPs
- Has the QA responsibility for GMP compliance of manufacture and analysis of IMP batches (in particular parenteral drug product batches)
- Reviews and approves GMP procedures, records and reports (e.g. SOPs, master batch records, discrepancy and change records and validation reports)
- Performs self-inspections in GMP plants and laboratories
- Reports directly to the RP and RP deputy
- Bachelor or Master Degree in Life Sciences or equivalent
- Experience in the pharmaceutical industry
- Experience in a GMP regulated environment
- Experience in all activities around parenteral manufacturing and quality control
- Demonstrated experience in a Pharmaceutical Technical Development environment.
- Knowledge of cGMP and Quality requirements for clinical development stages of biotechnological and/or parenteral IMPs (e.g. EU Annex 1)
- Experience in Discrepancy Management, CAPA, Technical Change Management (Veeva Vault) and Manufacturing Management (SAP), MES (PMX) and LIMS is an additional plus
- Ability to communicate clearly and professionally both verbally and in writing in English (C1) as well as in German (C1)
- World renowned company
- Future Career growth opportunities
Ihr Kontakt
Referenznummer
825582/1
Kontakt aufnehmen
Telefon:+41 44 225 50 00
E-Mail: positionen@hays.ch
Anstellungsart
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With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.
Mein Arbeitgeber
- IMP Quality Operations Switzerland is responsible for delivering Investigational Medicinal Products (“IMPs”) to patients in compliance with cGMP. They are the Quality Partner for all Manufacturing Units and Clinical Packaging in Pharmaceutical Technical Development in Switzerland and responsible for the Quality and Compliance oversight of all
Willy-Brandt-Platz 1-3
68161 Mannheim