Validation Engineer | Validierungsingenieur (m/w/d)

Randstad Professional

Ingelheim am Rhein, Rheinland-Pfalz, Deutschland
Published Feb 13, 2026
Full-time
Permanent

Job Summary

As a Validation Engineer in the pharmaceutical sector in Ingelheim, you will take full responsibility for the validation and qualification of production equipment, laboratory systems, GxP facilities, and technical building services. Your daily activities involve managing technical change controls, overseeing cleaning verifications, and ensuring the validated state of systems throughout their entire lifecycle. You will act as a critical interface between Quality, Compliance, and technical units, conducting root cause analyses for quality events and representing the department during international cGMP audits and inspections. This role is highly attractive for professionals seeking a stable, permanent position within a leading global recruitment network, offering a secure workplace, attractive benefits, and the opportunity to work on cutting-edge pharmaceutical infrastructure. The position combines technical expertise with strategic life-cycle management, allowing you to initiate improvement initiatives and lead external service providers in a highly regulated, high-stakes environment.

Required Skills

Education

University degree in Pharmaceutical Technology, Utility Engineering, Process Engineering, Mechanical Engineering, or a comparable technical discipline.

Experience

  • Professional experience in planning, constructing, and operating pharmaceutical plants
  • Experience in validation, qualification, and deviation management
  • Experience handling conversions and life-cycle projects within a pharmaceutical environment
  • Experience in project management and technical leadership of external service providers
  • Proven experience representing departments during international cGMP audits and inspections

Languages

German (Fluent)English (Fluent)

Additional

  • Location: Ingelheim; Full-time permanent contract; Requires expertise in international cGMP audits and inspections.