QA Manager Qualification

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View: 130

Update day: 22-04-2024

Location: Visp Valais VS

Category: Pharmaceutical / Chemical / Biotech

Industry: Ressources humaines et recrutement

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Job content

Owns all quality related responsibilities for the commissioning and qualification (C&Q)) activities of dedicated new facilities, equipment and utilities related to the GMP manufacturing of biologics & APIs. Representative of Quality in the CAPEX project organization in regards to qualification of facilities, utilities, equipment and systems (incl. computerized systems). Reviews and releases of qualification documents and SOPs. Be a Subject Matter Expert (SME) and provides guidance and recommendations to internal or external customers.

Firmenprofil
Pharma Industry

Arbeitsort
Visp

Arbeitsbeginn
Oktober

Motivation
A dynamic working environment focusing on career opportunities where multi-cultural teams from all over the world strive the best results.

Ausbildung
Bachelor, Master degree or PhD in biotechnology, chemistry, life science or related field

Erfahrungen
Significant experience in the GMP regulated pharmaceutical industry; preferable in a role within a Quality Unit. Strong background in cGMP. Broad knowledge in qualification of equipment, facilities, utilities (biopharmaceuticals & APIs) and related Guidelines (e.g. ASTM, ISPE, GAMP)

Sprachen
Deutsch: Of value
Englisch: Very good


Spezielles
If your device does not allow to include your CV, please forward it to i.vlas@universal-job.ch

Vakanz-Nummer
F-6-10645

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Deadline: 06-06-2024

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