Job Application

Our client, a Leading Life science organisation in the Basel area is looking for a QA Manager to support and oversee the end to end cGMP activities

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.

Main Tasks:

• Support and drive implementation of Annex 1 requirements during implementation in the Clinical Supply
• Responsible to represent Quality Assurance while driving all activities related to a successful implementation of Annex 1
• Maintaining and continuously supporting all Qualification/Validation and parenteral manufacturing activities
• Provide sound technical and quality assurance expertise for review and approval of quality related documents (eg SOPs, qualification, validation documents)

Requirements:

• Degree in Engineering, Pharmacy, Biology,
• Biochemistry, Chemistry, Life Science, Pharmacy or equivalent
• Min. 2-5 years experience in a GMP regulated environment and with Quality Systems, Quality assurance and OT
• Experience in Quality Risk Management as well as in performing risk assessments
• Experience in Qualification/Validation as
• well as all all activities around parenteral manufacturing
• Fluent in German, English B2

Job Title: QA Manager

Location: Basel, Switzerland

Job Type: Contract

Aerotek, an Allegis Group company. Allegis Group AG, Aeschengraben 20, CH-4051 Basel, Switzerland. Registration No. CHE-101.865.121. Aerotek and Actalent Services are companies within the Allegis Group network of companies (collectively referred to as "Allegis Group"). Aerotek, Actalent Services, Aston Carter, EASi, TEKsystems, Stamford Consultants and The Stamford Group are Allegis Group brands. If you apply, your personal data will be processed as described in the Allegis Group Online Privacy Notice available on the website.

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