Senior Pharmaceutical Manufacturing Supervisor

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.

• 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.

• 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.

• 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.