QA Operations Specialist

Job description:

On behalf of our client, a leading pharmaceutical company, we are seeking a QA Operations Specialist to support Drug Product Services (DPS) in Visp, ensuring quality oversight and compliance in a GMP-regulated environment.

About the customer:

The client is a leader in the Pharmaceutical industry, renowned for its innovative solutions and commitment to quality in healthcare.

Requirements:

• Quality Oversight: Act as the QA contact for drug product manufacturing operations, ensuring compliance with GMP standards and providing regular oversight on the shop floor, including cleanroom environments.
• Documentation Management: Assess, review, and approve GMP documents such as SOPs, risk assessments, deviations, investigations, CAPAs, change controls, and executed MBRs.
• Audit and Inspection Support: Represent QA during internal, customer, and regulatory audits and inspections.
• Training and Support: Provide GMP-related training to manufacturing personnel and support continuous improvement initiatives to enhance the Quality Management System (QMS) for DPS Visp.

Competences:

• Education: Master’s degree in Biotechnology or a related field.
• Experience:
• 3–5 years in a GMP-regulated environment with exposure to aseptic manufacturing activities.
• Previous experience within a Quality Unit and working with cross-departmental stakeholders.
• Languages: Fluent in English (written and spoken); knowledge of German is an advantage.
• Skills and Attributes:
• Strong organizational and analytical abilities.
• Detail-oriented and proactive with excellent communication skills.

Compensation benefits:

• A key role in ensuring compliance and quality within a leading biopharmaceutical organization.
• A collaborative and innovative work environment.
• Opportunities for professional development and growth.