Senior Production Pharmacist at Global Profilers

SUMMARY

We are seeking a dedicated Production Pharmacist to ensure that our production and manufacturing operations meet the highest compliance Standards, including GMP, and National Regulatory Authority Standards (NAFDAC, PCN, Federal Ministry of Labour and Productivity). This role is essential in ensuring product availability and quality and meeting the needs of Pharma Sales, marketing, and contract manufacturers.

Key Responsibilities

• Obtain batch-manufacturing records for planned production activities in collaboration with the Production Manager and other Sectional/Unit Heads.
• Ensure strict compliance with cGMP guidelines for all manufacturing and cleaning operations, working closely with Production Supervisors and Sectional/Unit Heads.
• Participate in batch production reviews for both in-house and Toll-manufactured products.
• Contribute to the creation of batch production records, SOPs, and other quality-related documentation as required, in coordination with Sectional/Unit Heads.
• Participate in qualification and validation activities within the R&D department.
• Collaborate on new projects and product development with the R&D Manager and other stakeholders.
• Oversee the proper maintenance of machinery and equipment in the Production department, in conjunction with Sectional/Unit Heads, Production Manager, and the Engineering department.
• Collect monthly production output data and other productivity reports as assigned by the Production Manager, in cooperation with other Sectional/Unit Heads and Supervisors in the department.
• Participate in internal self-inspections (GMP and ISO Quality Audit).
• Engage in quarterly and end-of-year stock counts in the Production department, working alongside Supervisors and other Sectional Heads.
• Approve instructions related to Oral Dosage forms production operations, including in-process controls, and ensure their strict implementation.
• Represent the department in QMS and cGMP activities.
• Coordinate QMS and cGMP documentation, implementation, and audit-related activities within the department.
• Share information on QMS and cGMP implementation with other staff in the department.
• Develop and implement Corrective Action and Preventive Action Plans for identified gaps (non-conformances) during inspections and ensure their resolution.
• Provide support to external auditors during compliance reviews.
• Participate in internal audits, contribute to report writing, and make presentations at monthly meetings as required.

Requirements

• Candidates should possess a Bachelor's In Pharmacy with at least 10-12 years’ work experience in any of the listed companies, TUYIL, FIDSON, EMZOR, ARCHY, PEACE, and BIORAJ.
• Good Knowledge of ICH guidelines.
• Technically Comprehensive.
• Fine Analytical Skills and Systematic approach.
• Proactive approach to problem-solving.
• Good computation Skills.
• Strong and consistent.
• Logical Interpretation of Data.
• Ability of multi-tasking.
• Fluent in English (Speaking, writing, reading, and understanding)
• Computer Skills (Ms. Excel, Ms. Word, Internet, Email)