The Production Manager will oversee all manufacturing operations related to pharmaceutical products, ensuring compliance with the Drug Act 1976 and its associated regulations. This role involves managing production batch records, coordinating with Quality Control, Research & Development, and Quality Assurance departments to maintain and improve product quality, validate equipment and processes, and introduce new products. The manager will also be responsible for preparing and updating standard operating procedures, procuring production supplies, supervising raw and packaging material handling, and maintaining communication with senior management regarding production progress. Ensuring quality checks, proper destruction of rejected materials, equipment maintenance, process validation, and personnel training are key aspects of this position. The role requires active participation in internal audits, risk management, and implementation of ISO standards (9001:2015, 14001:2015, and 45001:2018) within the department.
Key Responsibilities:
- Manage production functions related to manufacturing, packing materials, and finished products in compliance with pharmaceutical regulations.
- Maintain detailed and documented production batch records.
- Collaborate with QC Manager to address corrections and enhance product quality.
- Coordinate with R&D and QA teams for product and equipment validation, including qualification protocols and documentation.
- Support the introduction of new products in manufacturing, stability testing, and component development alongside R&D, QC, and QA departments.
- Prepare and update production and plant Standard Operating Procedures (SOPs).
- Identify and procure necessary production supplies and instrumentation, coordinating with the head office as needed.
- Guide raw and packaging material in-charges to ensure procurement meets quality standards and proper storage practices.
- Provide regular updates to the Director of Technical and General Manager of Plant Operations on production activities and progress.
- Conduct periodic quality checks throughout the production process.
- Oversee the approved destruction of rejected materials under direct supervision.
- Ensure maintenance of department premises and equipment.
- Verify that process validation and equipment calibration are performed, documented, and reported appropriately.
- Facilitate initial and ongoing training for production personnel.
- Support internal audits and self-inspections within the department.
- Review and approve risk and opportunity assessments, developing action plans to address weaknesses and capitalize on opportunities.
- Stay updated on industry knowledge, standards, and operational needs through continuous learning and participation in relevant events.
- Lead the implementation of ISO 9001:2015, 14001:2015, and 45001:2018 standards in the production department.
Required Qualifications:
- Bachelor of Pharmacy (B. Pharm), Doctor of Pharmacy (Pharm. D), or M.Phil degree.
- Minimum of 10 years of experience in Production or R&D within the pharmaceutical industry.
- At least 5 to 6 years of managerial experience in production or related departments.
Preferred Qualifications and Benefits:
- Commitment to ongoing professional development through training in pharmaceutical technology and related fields.
- Participation in seminars, workshops, and courses focused on production management, quality assurance, materials handling, and Current Good Manufacturing Practices (cGMP).
- Opportunities for advanced technical and management training.
- Full-time employment based in Lahore with morning shift hours.
- Competitive salary package.
This position requires a proactive leader with strong coordination skills and a thorough understanding of pharmaceutical production processes, quality standards, and regulatory compliance.