Onsite GMP QA Specialist — Biotech, Visp

Meet Life Sciences Ltd.; Oberwallis; On-site; CHF 75,000 - 110,000; Full time

Job summary

Meet Life Sciences Ltd. is seeking an experienced QA Specialist to support GMP quality activities at its Visp manufacturing site in Switzerland. You will help manage deviations, CAPAs, change controls, and quality documentation, ensuring compliance with GMP requirements and internal procedures.

You will collaborate with Manufacturing, QC and other teams to resolve quality issues, support inspections and audits, and contribute to continuous improvement initiatives on site in Visp.

Qualifications

• Experience in pharmaceutical/biotech QA environments.
• Solid understanding of GMP requirements and quality systems.
• Excellent communication and teamwork skills.

Responsibilities

• Support day-to-day QA operations within a GMP manufacturing environment.
• Manage deviations, CAPAs, change controls and quality documentation.
• Review batch manufacturing records and support batch disposition/release.
• Ensure compliance with GMP requirements and internal procedures.
• Assist with inspections, audits, and continuous improvement initiatives.
• Collaborate with Manufacturing, QC and cross-functional teams to resolve issues.

Skills

QA experience

GMP knowledge

Cross-functional collaboration

Job description

Meet Life Sciences Ltd. is seeking an experienced QA Specialist to support GMP quality activities at its Visp manufacturing site in Switzerland. You will help manage deviations, CAPAs, change controls, and quality documentation, ensuring compliance with GMP requirements and internal procedures.

You will collaborate with Manufacturing, QC and other teams to resolve quality issues, support inspections and audits, and contribute to continuous improvement initiatives on site in Visp.