Senior Quality Validation Specialist - Part-Time

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.