GMP Cordinator

Job summary

We are seeking a qualified and detail-oriented GMP Coordinator to join our Quality Operations team. The successful candidate will be responsible for ensuring compliance with Good Manufacturing Practice (GMP) requirements across manufacturing and quality operations, while supporting documentation, product quality reviews, stability monitoring, audits, and other quality assurance activities.

Min Qualification: Degree Experience Level: Mid level Experience Length: 3 years Language Requirement: English Working Hours: Full Time - 8 to 5 Applicant Location: Lagos, Nigeria

Job descriptions & requirements

Responsibilities:

• Monitor manufacturing processes and the plant environment to ensure compliance with GMP requirements and approved SOPs.
• Coordinate the calibration of balances and measuring devices across the plant.
• Verify manufacturing orders and coordinate sampling of intermediates for quality evaluation.
• Coordinate product stability studies and temperature mapping activities.
• Manage the issuance, retrieval, control, and archiving of GMP-related documents.
• Prepare and coordinate Product Quality Reviews (PQRs) and other quality reports.
• Ensure the use of approved and current documentation for manufacturing, packaging, and testing activities.
• Participate in internal quality, housekeeping and regulatory audits.
• Conduct GMP, GLP and laboratory safety training for relevant employees.
• Participate in the assessment of returned goods, product recalls and imported products.
• Support other Quality Assurance activities and deputize for the Quality Assurance Manager when required.

Requirements:

• Minimum of 3 years' relevant working experience in a pharmaceutical manufacturing environment, preferably within a Quality/Quality Assurance function.
• Minimum of a Bachelor's degree in Pharmacy, Biochemistry, Microbiology, or another relevant science-related discipline.
• Certification in a quality-related discipline will be an added advantage.
• Training or knowledge in Statistics and Pharmaceutical Quality Management is desirable
• Good knowledge of GMP and pharmaceutical manufacturing operations.
• Strong documentation and report-writing skills.
• Good supervisory and people-management skills.
• Strong organisational skills with excellent attention to detail and report writing.