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.