QC Validation Specialist

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

Key Responsibilities
• 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.

Qualifications
• 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, Analytical Balances, Incubators, Particle Counters, and similar equipment.
• Experience in pharmaceutical GMP environment.
• Knowledgeable in IQ, OQ, and PQ documentation and execution.
• Strong analytical, documentation, and communication skills.

Apply now and be part of a team committed to quality and compliance.