Compliance Specialist

Nyon, Canton of Vaud

Start: Early November 2026 (ASAP)

Contract: Temporary assignment 7 months

About

For one of our international partners in the pharmaceutical sector based in the Nyon region, we are looking for a Compliance Specialist to strengthen the site’s quality activities.

Within a demanding GMP environment, you will be a key player in managing deviations, quality investigations and CAPA. You will work closely with the Production, Maintenance, Quality and Technical Operations teams to ensure operational compliance and support continuous improvement of the quality system.

Your responsibilities

• Manage and document deviations in Veeva Quality in collaboration with the relevant teams.
• Ensure follow-up of deviations until their closure within the allotted time.
• Lead quality investigations as Lead Investigator.
• Identify root causes using structured problem-solving methodologies.
• Implement and monitor CAPA (Corrective and Preventive Actions).
• Participate in managing Change Controls and compliance activities.
• Conduct thorough analyses using tools such as 5 Why, Ishikawa or other investigation methodologies.
• Contribute to drafting and updating quality documents (SOPs, Work Instructions, Forms).
• Participate in quality gemba and promote good GMP practices on site.
• Support continuous improvement projects and optimisation of quality processes.

Your profile

• Minimum 2 to 3 years of Quality experience within a pharmaceutical GMP environment.
• Proven experience in managing deviations, investigations and CAPA.
• Good understanding of regulatory requirements and pharmaceutical quality systems.
• Experience with Veeva Quality highly appreciated.
• Professional French and English required.

Personal qualities

• Rigour and organisational skills.
• Excellent analytical abilities.
• Strong quality orientation and continuous improvement focus.
• Ease in cross-functional communication with different departments.
• Team spirit and solution-oriented approach.