What you will do
Supervise all production activities in compliance with cGMP and Standard Operating Procedures (SOPs)
Ensure proper handling, weighing, and dispensing of raw materials per batch manufacturing records
Coordinate with Quality departments for timely release of raw materials, intermediates, and finished goods
Investigate and report non-conformances or deviations in the production process
Train, guide, and supervise production operators on safety and operational protocols
Requirements
B.Pharm or MSc Pharmacy (or related field)
Minimum 5 years post-NYSC experience in a pharmaceutical or bio-pharmaceutical industry
Must be a licensed pharmacist registered with the Pharmacists Council of Nigeria (PCN)
Sound knowledge of cGMP, regulatory requirements, and pharmaceutical production practices
Strong communication, leadership, documentation, and problem-solving skills