Validation Engineer

About the role

The Validation Engineer supports the full validation lifecycle for direct, indirect and no‑impact systems within a regulated pharmaceutical environment. The role ensures equipment and systems stay qualified, maintains compliance with GMP standards, and contributes to audit readiness.

Key responsibilities

• Perform validation maintenance reviews for all system categories.
• Generate, review and approve validation documentation (DQ, IQ, OQ, PQ) for new equipment.
• Plan and execute periodic re‑qualification protocols for temperature chambers using data loggers and sensors.
• Coordinate schedules and activities with QA, QC and Engineering teams.
• Ensure all validation work complies with GMP and internal quality standards.
• Maintain accurate documentation to support audit readiness.

Required profile

• Diploma or degree in Engineering, Life Sciences, Pharmacy or a related field.
• Experience in validation or qualification activities within a GMP‑regulated environment.
• Familiarity with DQ, IQ, OQ, PQ documentation.
• Understanding of temperature mapping, calibration and equipment qualification processes.
• Strong attention to detail and ability to manage multiple tasks.
• Effective communication skills for cross‑functional coordination.

Required skills

• DQ/IQ/OQ/PQ documentation
• Temperature mapping
• Calibration procedures
• Equipment qualification
• GMP compliance
• Data logger and sensor usage

What we offer

• Generous leave policy.
• Comprehensive medical and dental coverage.
• Continuous professional development programs.
• Inclusive culture that promotes innovation and collaboration.