On-Site CQV Engineer: GMP Validation & Vendor Oversight

agap2 Switzerland; Bern; Sur place; CHF 110 000 - 150 000; Plein temps

Avantages offerts par ce poste

Challenging projects

Training and career development

Solid local leadership

Résumé du poste

agap2 is seeking a CQV Engineer for on-site work in Switzerland. You will support validation activities from installation through commissioning and qualification, ensuring GMP compliance and timely delivery.

This role requires 3+ years in CQV within pharma/biotech, fluency in German or English, and a strong track record of DQ/IQ/OQ/PQ execution, risk assessment, and collaboration with vendors. Join a team with challenging projects and strong local leadership.

Qualifications

• Bachelor's or Master's in Engineering, Pharmaceutical Sciences, or related field.
• 3+ years CQV experience in GMP pharma/biotech.
• Fluent in German and/or English.

Responsabilités

• Execute and approve DQ, IQ, OQ, and PQ activities.
• Ensure CQV milestones and timelines are met.
• Supervise vendors and validate commissioning quality.
• Generate and review validation protocols, reports, and technical documentation.
• Track deviations, non-conformances, and CAPAs.
• Assess project risks and implement corrective actions.

Formation

Engineering or Pharmaceutical Sciences degree

Outils

CQV protocols

Description du poste

agap2 is seeking a CQV Engineer for on-site work in Switzerland. You will support validation activities from installation through commissioning and qualification, ensuring GMP compliance and timely delivery.

This role requires 3+ years in CQV within pharma/biotech, fluency in German or English, and a strong track record of DQ/IQ/OQ/PQ execution, risk assessment, and collaboration with vendors. Join a team with challenging projects and strong local leadership.