QA Expert - Senior

For one of our clients, a global pharmaceutical company, we are currently looking for a Quality Assurance Expert - Senior.

General Information: 

• Start date: 16.03.2026 
• End date: 17.07.2026 
• Workplace: Neuchatel
• Workload: 100%
• Home Office: possible, max 20%
• Working Hours: Standard, during aseptic simulation tests: 2*8 shifts (morning 06h00-14h30, Afternoon 14h00-22h30)

About the job: 
The objective of this role within the Quality Ops organization is to provide support as a Quality Assurance Senior Expert during the implementation of a new Fill & Finish line. The candidate may also be involved in routine GMP operations for the Fill & Finish area. They must ensure the quality of information reported within various systems and documentation in compliance with current guidelines, internal standards, and regulatory requirements.

Reports to the QA Manager, with daily interaction with Manufacturing, Engineering, Sterility Assurance, Quality Ops, Training, etc.

Tasks & responsibilities: 

• Approve "on-the-floor" aseptic interventions performed by manufacturing during Aseptic Process Simulations (APS).
• Review Master Batch Records.
• Attend all relevant meetings to perform the tasks mentioned above.
• Strictly follow the escalation process.
• Ensure completion of relevant training and software access management according to company policies.
• Support the team with other conventional quality oversight tasks as requested (e.g., continuous improvement initiatives, GMP tours in classified areas, etc.).

Requirements: 

• Academic technical or scientific background (Master’s degree / Bac +5).

• 2–3 years of operational cGMP experience in a Quality Ops department at a pharmaceutical production site for sterile injectable products.

• Holistic understanding of production processes (from cell culture to aseptic filling), including unit operations, equipment, gowning, environmental monitoring, and physicochemical/biological laboratory testing.

• Strong knowledge of Quality frameworks (cGMP) and Quality Systems (Deviations, CAPA, Change Control, Training, Documentation, etc.).
• Excellent written and oral proficiency in both French and English.
• Proficient in MS Office/PC-based work.
• Team player, agile, and autonomous.

Sounds interesting? Apply now – we’re looking forward to receiving your applications!