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 equipmen...