About the Role
Our client, a dynamic pharmaceutical manufacturer, is seeking an experienced and highly motivated Senior Pharmaceutical Manufacturing Supervisor to oversee daily operations at their facility in Rustenburg. This role is crucial for ensuring efficient, compliant, and safe production of pharmaceutical products. The ideal candidate will possess a strong understanding of manufacturing processes, GMP principles, and team leadership. Joining our client offers a significant opportunity to contribute to the production of vital medicines and advance your career within a growing organization in the North West province. You will be responsible for managing a production team, optimizing workflows, and upholding the highest standards of quality and safety. This position requires hands‑on supervision and a commitment to operational excellence within the manufacturing environment.
Key Responsibilities
- Supervise and direct the activities of pharmaceutical manufacturing personnel to ensure production targets are met efficiently and safely.
- Ensure all manufacturing operations are conducted in strict compliance with current Good Manufacturing Practices (cGMP) and company standard operating procedures (SOPs).
- Monitor production processes, identify potential issues, and implement corrective actions to maintain product quality and yield.
- Train and mentor production staff on equipment operation, safety procedures and GMP requirements.
- Oversee the accurate documentation of all manufacturing activities, including batch records, logs and equipment usage.
- Participate in the investigation of deviations, out‑of‑specification (OOS) results, and customer complaints related to manufacturing.
- Collaborate with Quality Assurance, Quality Control, Engineering and Maintenance departments to resolve production challenges and support continuous improvement initiatives.
- Ensure the proper use and maintenance of manufacturing equipment and facilities.
- Promote a culture of safety, quality, and accountability within the production team.
- Contribute to the planning and scheduling of production activities to meet demand.
Requirements
- Diploma or Bachelor's degree in a relevant scientific or technical field (e.g., Chemical Engineering, Pharmacy, Industrial Technology).
- Minimum of 5 years of experience in pharmaceutical manufacturing, with at least 2 years in a supervisory or team lead role.
- Thorough understanding of cGMP, pharmaceutical manufacturing processes, and relevant regulatory requirements.
- Proven ability to manage and motivate a production team effectively.
- Strong knowledge of documentation practices within a regulated environment.
- Excellent problem‑solving, decision‑making, and organizational skills.
- Good communication and interpersonal skills.
- Experience with specific dosage forms (e.g., solid dosage, sterile injectables) is a plus.
- Must be based in or willing to relocate to the Rustenburg area.
Benefits
- Competitive salary and performance-based bonuses.
- Comprehensive health and retirement benefits package.
- Opportunities for professional development and further training.
- Paid time off and holiday leave.
- A stable and supportive work environment within a key industry.
- Chance to contribute to the production of essential medicines.
- Potential for career advancement within the company.