Job Summary

The Production Pharmacist is responsible for planning, supervising, and coordinating pharmaceutical manufacturing activities to ensure products are produced according to approved specifications, current Good Manufacturing Practices (cGMP), company policies, and regulatory requirements. The role ensures product quality, efficiency, safety, and compliance throughout the manufacturing process.

Key Responsibilities

Production Operations

• Supervise the manufacturing of pharmaceutical products, including tablets, capsules, syrups, ointments, and other dosage forms.
• Ensure production activities are carried out according to approved Batch Manufacturing Records (BMRs) and Standard Operating Procedures (SOPs).
• Monitor production schedules to meet delivery targets and customer requirements.
• Ensure proper utilization of manpower, equipment, and materials.

Quality and Compliance

• Ensure compliance with cGMP, regulatory requirements, and company quality standards.
• Review and verify batch manufacturing documentation for accuracy and completeness.
• Participate in investigations related to deviations, non-conformances, and customer complaints.
• Support internal and external audits and regulatory inspections.

Equipment and Facility Management

• Ensure production equipment is properly cleaned, maintained, and calibrated.
• Monitor environmental conditions in production areas.
• Coordinate preventive maintenance activities with the engineering department.

Personnel Management

• Train and supervise production operators and technicians.
• Ensure adherence to health, safety, and hygiene requirements.
• Conduct performance evaluations and recommend training needs.

Inventory and Material Control

• Verify the availability and proper use of raw materials and packaging materials.
• Monitor material consumption and minimize wastage.
• Ensure proper storage and handling of materials in compliance with GMP requirements.

Documentation

• Maintain accurate production records and reports.
• Prepare daily, weekly, and monthly production reports.
• Ensure all manufacturing documentation is completed and archived according to GMP requirements.

Qualifications

• Bachelor of Pharmacy (B.Pharm) degree.
• Registered Pharmacist with the relevant Pharmacy Regulatory Authority.
• 2–5 years of experience in pharmaceutical manufacturing (or as required).
• Sound knowledge of cGMP, GDP, and pharmaceutical manufacturing processes.

Skills and Competencies

• Strong leadership and supervisory skills.
• Knowledge of pharmaceutical production equipment and processes.
• Excellent documentation and record-keeping skills.
• Good problem-solving and analytical abilities.
• Strong communication and teamwork skills.
• Proficiency in Microsoft Office applications.

Key Performance Indicators (KPIs)

• Production output achievement.
• Batch right-first-time rate.
• GMP compliance level.
• Reduction in production deviations and wastage.
• Equipment utilization and downtime control.
• Timely completion of production schedules.

Additional Information

Location: Pharmaceutical Manufacturing Plant, Ogidi, Anambra State.

Salary: Negotiable.

Reports To: Production Manager / Plant Manager.

Method of Application

Interested and qualified candidates should forward their CV to: recruitment.dtnl@gmail.com, using the position as the subject of the email.

Disclaimer: This job description has been reformatted by AI for readability. Please verify all details with the employer before applying.