or our client, an international company based in Neuchâtel, we are looking for a QA Senior Expert.

General Information:

• Start date: ASAP
• End date: 31.12.2025
• Extension: possible, to be discussed
• Workplace: Neuchâtel
• Workload: 100%

Tasks and responsibilities:

• Responsible for Quality Assurance in the frame of activities all along the manufacturing and release process.
• QA representative for both routine GMP activities and company projects.
• Quality partner within Production Unit Team and the Quality Control laboratories, Warehouse and Engineering/Maintenance departments as applicable.
• Ensure quality of information within systems and documentation in respect to current guidelines, compliance and regulatory requirements.
• Participation in GMP audits and shopfloor.
• Promote and be involved in Continuous Improvement.
• Understand and apply company EHS guidelines and commitments policy, take care of its own safety, report risk situations and improvement opportunities to supervisory personnel.
• Can act as back up of other QA Senior experts and QA Lead as requested.

Your profile:

• At least 7 years of experience in an GMP environment
• University degree in Engineering, Biotechnology, Pharmacy or Quality Management applied to industrial process or equivalent experience in pharmaceutical and /or biotechnological companies
• Fluent French and a good command of English
• Demonstrate the company Values of Integrity, Fairness, Honesty, Perserverence as a natural way of working
• Good knowledge of FDA, EMA, ICH regulations, Pharmacopeias and Quality system standards
• Knowledgeable in auditing and inspection against regulatory / Quality standards
• Knowledge/Experience with Quality tools such as Trackwise
• Good analytical skills and ability to simplify the complex
• Solution oriented and team spirit
• Good listener and communication skills
• Good organizational skills and continuous improvement mindset