Required skills
Job description
Project overview
We are looking for a candidate with a first experience within Quality Assurance in the biopharmaceutical industry.
Responsibilities
What we’re looking for:
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Job profile (1K5PE9)
Life Sciences - Quality Management
Wallis
Contracting
Full Time
Quality Assurance
- Perform timely and independent review of executed electronic batch records (eBRs) in MES Syncade.
- Ensures that operations batch records are accurately executed, complete, and ready for QA review.
- Collaborate with Manufacturing and Quality teams to clarify and resolve documentation issues
- Initiate and support in the management of Quality Records (CAPAs and Deviations) for Batch Record review related observations.
- Support preparation of documentation package to enable fast release by QA.
- Previous experience in GDP and GMP regulated pharmaceutical / API industry.
- Experience in batch record review (preferred eBR) OR in manufacturing is required.
- Ability to identify non-compliance and gaps from quality standards.
- Very good communication skills and interaction with all kinds of interfaces within the organization; strong team orientation.
- Structured, focused and well-organized working attitude.
- Open-minded for new ideas and suggestions; solution-oriented.
- Agile, highly motivated and dynamic drive.
- Ability to produce reliable results under stress.
Project details
- Start: flexible
- Location: Wallis, CH
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