i-Pharm Consulting

QA Ops. Manager (m/f) Switzerland

Location
Switzerland
Salary
Negotiable
Posted
05 Dec 2018
Closes
19 Dec 2018
Ref
mgb05122018
Contract Type
Permanent
QA Ops. Manager (m/f) in Switzerland

We are currently looking for a QA ops. Manager (m/f) that holds a master’s degree with 5 years of experience in clinical trials and QA. In this role you will work 100% office based at our client’s site in the French part of Switzerland. Here, you will mainly focus on ensuring the compliance of regulatory, ethical and GXP practices requirements as well as training and managing the audits.

Language Requirements: Fluency in English, German and French are a plus.
Employment Type: Permanent
Salary: Competitive basic salary with pension scheme

Responsibilities:

• Responsible for batch record disposition for manufactured products for Clinical Trials.
• Review and approve batch records, formulation records, validation reports, stability protocols, product specification sheets, M/WCB records, IND/IMPD and development reports.
• Review and approves deviations.
• CAPA management.
• Support GMP compliance for the projects.
• Provide GMP training to QA and other departments.

Profile:

• Minimum 5 years of relevant experience in QA.
• Experienced in GMP guidelines
• Manufacturing USP and Quality Control experience is a plus.
• Experience with Quality Systems
• Ability to work independently.
• Advanced post graduate degree or graduate degree.
• Fluency in written and spoken English other languages are a plus.

For further information please do not hesitate to contact Mario Becerra, Recruitment Consultant at I-Pharm Consulting +41 (0) 61 588 02 03. Please send your application documents to:
mbecerra@i-pharmconsulting.com

If this role doesn’t apply to you, feel free to contact Mario for further discussion on other career opportunities. In case you know someone in your network that could be interested, feel free to provide him/her with Mario’s contact details and he will be at their disposal.

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