Quality Assurance Specialist

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

I'm currently supporting a leading biotechnology organisation in Switzerland seeking an experienced QA Specialist to support GMP quality activities at its manufacturing site in Visp.

Key Responsibilities:

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

Requirements:

• Previous QA experience within pharmaceutical or biotechnology manufacturing.
• Strong understanding of GMP requirements and quality management systems.
• Experience with deviations, CAPAs, change controls and batch documentation.
• Excellent communication and cross-functional collaboration skills.
• Ability to work onsite in Visp, Switzerland.