Senior QA Specialist

Senior QA Specialist

Lonza

Visp, Switzerland

Key responsibilities:

• Participation in the preparation, review, and approval of process-specific PQRs.
• Evaluation and approval of change requests, deviations, and SOPs related to PQRs.
• Supporting project teams to ensure compliance with Lonza SOPs for PQR, CPV, and related documentation.
• Preparation and approval of the monthly PQR newsletter.
• Maintaining the PQR status overview list.
• Active participation in and contribution to the validation team to share knowledge and further develop best practices.
• Acting as the point of contact for PQR/CPV during customer audits.

Key requirements:

• M.Sc. degree in a life sciences discipline.
• Ideally, initial experience in PQR and CPV (Stage 3 of PPQ), with a strong background in cGMP regulations.
• Fluency in English (written and spoken); fluency in German is preferred.
• Ability to manage multiple tasks effectively and meet deadlines.
• A collaborative team player with a willingness to learn and grow alongside the team.
• Exceptional interpersonal and communication skills, both verbal and written.
• Solution-oriented mindset with a strong focus on teamwork.
• Ability to oversee project execution and identify non-compliance with procedures.
• Highly structured, focused, and well-organized approach to work; open to new ideas and suggestions; agile, highly motivated, and driven.

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Switzerland      Manufacturing and Logistics      On-site      Quality Assurance      Lonza