QC Validation Specialist

Responsible for qualification, requalification, relocation, decommissioning, and retirement of GMP laboratory equipment while ensuring compliance with GMP and regulatory requirements within the pharmaceutical industry.

• Perform qualification and validation activities for GMP laboratory equipment.
• Execute and support IQ, OQ, and PQ protocols and reports.
• Support equipment relocation, requalification, decommissioning, and retirement activities.
• Ensure compliance with GMP, data integrity, and regulatory requirements.
• Maintain accurate validation documentation and records.

• Diploma or Bachelor’s Degree in any Engineering field.
• Minimum of 5 years of relevant experience in GMP laboratory equipment qualification and validation.
• Hands‑on experience with analytical instruments such as HPLC, UV‑Vis Spectrometer, TOC Analyzer, CE...