Senior Specialist Quality Assurance

For our client in Visp, we are looking for a Senior QA Specialist. It is a contract until 30 July 2027.

Location: Visp

Contract start date: As soon as possible

Contract end date: 30 July 2027

Key responsibilities:

Responsible for project specific QA Operation work during commissioning/qualification and project tech transfer in Vibe-X
Assess and manage tasks that would impact Quality operation during GMP manufacturing
Plan for future activities and coordinate with other departments (e.g. QC, Engineering, Manufacturing) to complete the planned activities
Support day-to-day Quality Assurance activities in accordance with approved SOPs/Policies for a GMP manufacturing facility
Review GMP records to ensure compliance with cGMP per written procedures
Make real-time decisions on process events on the floor, based on knowledge of defined SOPs & policies
Participate in walkthroughs and audit/inspections

Key requirements:

Bachelor of Science in Life Science or a related field
Significant experience in the pharmaceutical quality area
Work experience in a role in Quality Assurance, Production or Engineering, in pharmaceutical industries and cGMP controlled environment. QA experience in tech transfer is preferred
Excellent knowledge of computer systems (e.g. TW, SAP, etc.) and quality tools such as risk based approaches (e.g. FMEA)
Fluency in English