QA specialist M/F

• 10 septembre 2026
• 100%
• Durée indéterminée
• français (Intermediate)
• Avenue de la gare, 1895 Vionnaz

Expleo offers a unique range of integrated engineering, quality, and strategic consulting services for digital transformation. In a context of unprecedented technological acceleration, we are the trusted partner of companies that innovate. We help them develop a competitive advantage and improve the daily lives of millions of people.

Joining Expleo Group means 17,000 employees in 30 countries but also:

• Having technical and human support for every project and high-performance career monitoring.
• Undertaking training to develop your professional capabilities.
• Participating in dedicated special events.
• Joining a dynamic team.

To support our growth in Suisse Romande, in the canton of Valais, we are looking for a consultant:

QA specialist M/F

Your mission

Within a demanding GMP environment, you ensure quality support for production operations and ensure the compliance of activities with regulatory requirements and current quality standards. As a true partner to the operational teams, you contribute to guaranteeing product quality while supporting continuous improvement activities.

Your responsibilities

• Provide daily quality support to production teams.
• Ensure the compliance of operations with GMP requirements and internal procedures.
• Participate in the management of quality events: deviations, investigations, CAPA and change controls.
• Perform the quality evaluation of production files and guarantee their compliance.
• Support operational teams in resolving quality issues.
• Participate in risk analyses and continuous improvement activities.

Your profile

• University degree or equivalent in the fields of life sciences, pharmacy, biotechnology, or quality.
• You have a minimum of 3 years of experience in pharma or Biotech QA, imperatively acquired in a GMP environment: Management of deviations, CAPA, investigations or change controls and batch release.
• Ideally, you have participated in industrial projects / process transfers for highly potent active pharmaceutical ingredients (HPAPI).
• You have an analytical mind, rigor, and the ability to make quality decisions in a highly regulated environment.
• You speak French fluently and have a professional level of English.

Avenue de la gare
1895 Vionnaz