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Pharmaceutical Manufacturing Supervisor - Bulk Production

Job in Rustenburg, 0202, South Africa
Listing for: Placements24
Full Time position
Listed on 2026-10-19
Job specializations:
  • Manufacturing / Production
    Production Manager, Pharmaceutical Manufacturing, Manufacturing & Industrial Operations
Job Description & How to Apply Below
About the Role

Our client, a rapidly expanding pharmaceutical manufacturing company, is seeking an experienced and diligent Pharmaceutical Manufacturing Supervisor to oversee bulk production operations at their facility located in
** Rustenburg, North West**. This critical role involves leading a team of production operators and technicians, ensuring the efficient and compliant manufacturing of high-quality pharmaceutical products. You will be responsible for managing day-to-day production activities, adhering strictly to Good Manufacturing Practices (GMP), and maintaining optimal operational efficiency. The ideal candidate will possess strong leadership skills, a thorough understanding of pharmaceutical production processes, and a commitment to safety and quality.

This position offers an excellent opportunity to contribute to a vital industry and advance your career in manufacturing management within a reputable organization in
** Rustenburg**.

Key Responsibilities
  • Supervise and coordinate the daily activities of the pharmaceutical bulk production team, ensuring adherence to production schedules.
  • Ensure all manufacturing activities are conducted in strict compliance with GMP, regulatory requirements, and internal SOPs.
  • Monitor production processes, identify deviations, and implement corrective actions promptly.
  • Train and mentor production staff on proper operating procedures, safety protocols, and quality standards.
  • Oversee the operation and maintenance of manufacturing equipment, ensuring optimal performance and cleanliness.
  • Manage raw material inventory and ensure timely requisition of materials for production runs.
  • Conduct regular safety inspections and enforce safety regulations within the production area.
  • Participate in investigations of production deviations and quality issues, implementing effective root cause analysis.
  • Contribute to process improvement initiatives aimed at enhancing efficiency, reducing waste, and improving product quality.
  • Maintain accurate production records, batch documentation, and performance logs.
Requirements
  • National Diploma or Bachelor's degree in Chemical Engineering, Pharmacy, Biotechnology, or a related scientific/technical field.
  • Minimum of 5 years of experience in pharmaceutical manufacturing, with at least 2 years in a supervisory or team lead role.
  • Strong understanding and practical application of Good Manufacturing Practices (GMP).
  • Proven experience in supervising production teams and managing operational schedules.
  • Familiarity with various pharmaceutical production equipment and processes (e.g., blending, granulation, drying, tablet compression).
  • Excellent leadership, communication, and problem-solving skills.
  • Ability to work effectively in a fast-paced manufacturing environment.
  • Commitment to upholding high standards of safety and quality.
  • Proficiency in documentation and record-keeping.
  • Willingness to work shifts if required by the production schedule in
    ** Rustenburg, North West**.
Benefits
  • Our client offers a competitive salary, comprehensive medical aid, and a retirement fund.
  • Opportunities for professional development and training in advanced manufacturing techniques are available.
  • Employees benefit from a supportive work environment, structured career progression pathways, and paid time off.
  • The company is committed to fostering a safe and inclusive workplace in
    ** Rustenburg, North West**, where employees can thrive and contribute to the company's mission of delivering high-quality pharmaceutical products.
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