GMP Validation & Commissioning Engineer

LHH; Schachen; Sur place; CHF 90 000 - 130 000; Plein temps

Résumé du poste

LHH is seeking a motivated Qualification / Computer System Validation Engineer to support qualification and validation activities within a pharmaceutical environment in Switzerland. The role requires hands-on qualification/validation experience across lab instruments, manufacturing equipment, clean room systems, utilities, and facilities, plus governing computer system validation in GMP settings.

The ideal candidate holds a bachelor’s degree in a related field and at least five years of

Qualifications

• Bachelor’s degree in Engineering, Pharmacy, Chemistry, Biotechnology, Microbiology, or related scientific discipline.
• Minimum 5 years of Qualification/Validation experience.
• Strong knowledge of GMP / cGMP principles and practices.
• Hands-on in Qualification/Validation and Computer System Validation.

Responsabilités

• Manage qualification and validation activities for lab instruments, manufacturing and clean room equipment, utilities, and facilities.
• Prepare, review, and execute qualification and validation documentation (protocols, reports, assessments).
• Provide oversight for computer system validation in manufacturing and quality environments.
• Ensure activities comply with cGMP, regulatory requirements and company standards.
• Collaborate with Production, QC, and Engineering across projects.
• Support audits, inspections and quality improvement initiatives.
• Review GMP-related documents (technical assessments, deviations, CAPAs, change controls).
• Contribute to continuous improvement of qualification and validation processes.

Connaissances

GMP knowledge

Computer System Validation

Analytical problem solving

Documentation

Independent / collaborative work

Formation

Bachelor's degree in Engineering/Pharma/chemistry/biotech

Outils

VeevaVault

Kneat

Description du poste

LHH is seeking a motivated Qualification / Computer System Validation Engineer to support qualification and validation activities within a pharmaceutical environment in Switzerland. The role requires hands-on qualification/validation experience across lab instruments, manufacturing equipment, clean room systems, utilities, and facilities, plus governing computer system validation in GMP settings.

The ideal candidate holds a bachelor’s degree in a related field and at least five years of