Pharmaceutical Manufacturing Supervisor - Bulk Production

Placements24; Rustenburg; On-site; ZAR 550,000 - 850,000; Full time

Benefits offered by this job

Competitive salary

Medical aid

Retirement fund

Professional development

Job summary

Placements24 is seeking an experienced Pharmaceutical Manufacturing Supervisor in Rustenburg, North West to lead the bulk production team and ensure GMP-compliant operations.

The role requires a relevant scientific/technical degree and at least 5 years in pharma manufacturing, including 2 years in supervision, with strong leadership and problem-solving skills.

Qualifications

• Bachelor’s degree or National Diploma in a relevant science/engineering field.
• Proven leadership and supervisory experience in pharmaceutical manufacturing.
• GMP knowledge and practical application in a production environment.

Responsibilities

• Supervise bulk production team to meet production schedules.
• Ensure activities comply with GMP, regulatory requirements and SOPs.
• Monitor processes, identify deviations, and implement corrective actions.
• Train and mentor staff on procedures, safety and quality standards.
• Oversee equipment operation, maintenance and cleanliness.
• Manage raw material inventory and material requisitions.
• Conduct safety inspections and enforce regulations.
• Investigate deviations and quality issues with root-cause analysis.
• Participate in process improvements to reduce waste and boost quality.
• Maintain production records, batch docs, and logs.

Education

National Diploma or Bachelor's degree in Chemical Engineering, Pharmacy, Biotechnology, or a related scientific/technical field

Job description

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.