Documentation & In‑Process Officer – Pharmaceutical Manufacturing

About the role

Morison Industries Plc is seeking a meticulous Documentation & In‑Process Officer to join its pharmaceutical manufacturing team in Ikeja, Lagos. The role ensures that all production documentation is accurate, complete, and compliant with GMP, SOPs, and regulatory standards.

Key responsibilities

• Prepare, issue, reconcile, and archive Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs) and other controlled production documents.
• Review production documentation for completeness, accuracy and compliance before submission to Quality Assurance.
• Perform and document in‑process quality checks during manufacturing and packaging operations.
• Monitor critical process parameters and verify line clearance activities before production starts.
• Record, investigate and report in‑process deviations, non‑conformances and abnormalities.
• Maintain real‑time production records in line with ALCOA+ data‑integrity principles.
• Coordinate with Production, QA and QC to resolve documentation discrepancies.
• Assist in GMP documentation training for production personnel.
• Participate in internal audits, regulatory inspections, process validation and continuous‑improvement initiatives.
• Manage, distribute and archive controlled documents according to document‑control procedures.

Required profile

• Bachelor’s degree in Pharmacy, Biochemistry, Microbiology, Industrial Chemistry or a related scientific field.
• Strong attention to detail and a quality‑focused mindset.
• Ability to work effectively in a regulated manufacturing environment.

Required skills

• Good Manufacturing Practices (GMP)
• Good Documentation Practices (GDP) and ALCOA+ data‑integrity principles
• Batch Manufacturing Record (BMR) and Batch Packaging Record (BPR) management
• In‑process quality monitoring and deviation reporting
• Regulatory compliance and SOP adherence