QA Product Lead, GMP Quality Ops (Visp)

EFOR; Oberwallis; On-site; CHF 120,000 - 170,000; Full time

Job summary

EFOR is seeking an experienced QA Product Lead to join a growing pharmaceutical manufacturing organization in Visp. This role provides quality oversight for GMP manufacturing and ensures compliant batch release.

You will collaborate with Production, QC and Technical Operations to drive improvements, lead investigations, CAPAs and changes, and support regulatory audits. On-site presence in Visp is required.

Qualifications

• Bachelor's or Master's degree in Life Sciences, Pharmacy, Biotechnology, Chemistry or related field.
• Minimum 8 years of experience within the pharmaceutical or biotechnology industry.
• Strong experience in QA Operations, Product Quality or Batch Release environments.
• Solid understanding of GMP regulations and pharmaceutical manufacturing processes.
• Experience with deviations, CAPAs, investigations and change controls.
• Ability to work cross-functionally within a manufacturing environment.
• Strong communication and stakeholder management skills.

Responsibilities

• Provide Quality oversight for GMP manufacturing operations
• Review and approve batch documentation and production records
• Support batch disposition and release activities
• Partner closely with Manufacturing, QC and Technical Operations teams
• Lead investigations, deviations, CAPAs and change controls
• Ensure compliance with GMP requirements and regulatory expectations
• Act as the Quality representative for assigned products and manufacturing processes
• Drive continuous improvement initiatives across Quality and Operations
• Support inspection readiness and regulatory audits

Skills

QA Operations

Product Quality

Batch Release

Cross-functional collaboration

Regulatory readiness

Education

Bachelor's or Master's in Life Sciences / Pharmacy / Biotechnology / Chemistry

Job description

EFOR is seeking an experienced QA Product Lead to join a growing pharmaceutical manufacturing organization in Visp. This role provides quality oversight for GMP manufacturing and ensures compliant batch release.

You will collaborate with Production, QC and Technical Operations to drive improvements, lead investigations, CAPAs and changes, and support regulatory audits. On-site presence in Visp is required.