Senior Quality Validation Specialist

Job Summary Responsible for qualification and validation activities for laboratory systems and equipment, ensuring compliance with GMP and regulatory requirements within a pharmaceutical manufacturing environment. Key Responsibilities • Perform qualification and validation activities for laboratory systems and equipment. • Execute and support IQ, OQ, and PQ protocols and reports. • Support implementation, requalification, relocation, and retirement of validated systems. • Ensure compliance with GMP, data integrity, and regulatory requirements. • Maintain accurate validation documentation and records. • Coordinate with cross-functional teams to support validation projects and system compliance. Qualifications • Diploma or Bachelor’s Degree in Engineering, Life Sciences, or related field. • Minimum of 5 years of experience in a regulated pharmaceutical manufacturing environment. • At least 3 years of hands-on experience in validated laboratory systems qualification. • Hands-on experience and understanding of automated systems supporting pharmaceutical manufacturing and laboratory operations. • Knowledgeable in validation lifecycle, GMP, and data integrity requirements. • Strong analytical, documentation, and communication skills. Apply now and join a team committed to quality, compliance, and operational excellence.