• Application Deadline:
• Position: Production Manager



• Job Type Full Time



• Qualification BA/BSc/HND



• Experience 5 - 10 years



• Location Ogun




• Job Field Manufacturing  , Pharmaceutical 
  
  

Department: Associate Production Manager

Manufacturing / Production Reports To: Head – Plant Operations / Factory Manager

Job Summary

• The Production Manager will be responsible for planning, coordinating, and controlling manufacturing processes to ensure products are manufactured efficiently, on time, within budget, and to the required quality and regulatory standards.


• The role involves supervision of production staff, adherence to cGMP, and continuous improvement of production systems.

Key Responsibilities

• Plan and organize production schedules in alignment with demand forecasts and inventory levels.


• Ensure optimal utilization of resources -manpower, machines, and materials.


• Supervise and coordinate all manufacturing activities and staff in the department.


• Maintain strict adherence to current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs), and safety protocols.


• Collaborate with QA, QC, Engineering, and Supply Chain departments to ensure smooth operations.- Monitor production metrics and prepare daily, weekly, and monthly performance reports.


• Investigate and resolve production-related deviations, incidents, and complaints.


• Ensure timely maintenance and calibration of manufacturing equipment.


• Drive continuous improvement initiatives to enhance productivity, reduce downtime, and minimize waste.


• Train and mentor production staff to improve skills, compliance, and efficiency.


• Participate in audits (regulatory, internal, and customer) and ensure prompt closure of observations.- Comply with all local, national, and international regulatory and quality requirements

Qualifications and Experience

• Bachelor’s Degree in Pharmacy (B.Pharm)


• 5–10 years of progressive experience in pharmaceutical manufacturing, with at least 3 years in a supervisory or managerial role.


• Strong understanding of GMP, GDP, and other regulatory compliance (e.g., NAFDAC, WHO, FDA).


• Proven experience in tablet, capsule, liquid, or sterile dosage forms is an added advantage.


• Proficiency in production planning software and ERP systems (e.g., SAP,).


• Strong leadership, communication, and problem-solving skills.


• Ability to work under pressure and deliver results in a fast-paced environment.

Key Competencies:

• Leadership and team management


• Process and quality orientation


• Problem-solving and decision-making


• Attention to detail


• Time and resource management


• Compliance and documentation skills.