Production Supervisor - Pharmaceutical Chemicals

Placements24; Stellenbosch; On-site; ZAR 540,000 - 900,000; Full time

Benefits offered by this job

Health insurance

Retirement benefits

Paid time off

Job summary

Placements24 is seeking a Production Supervisor for our Paarl facility in the Western Cape. You will oversee daily chemical production operations, ensuring GMP compliance and achievement of manufacturing targets.

You will lead and train a team of production operators, driving safety, quality, and efficiency while collaborating with R&D, QA, and Maintenance to resolve challenges and implement process improvements.

Qualifications

• Bachelor's degree in Chemical Engineering, Chemistry, Pharmacy or related field.
• Minimum 5 years in chemical production with ≥2 years in supervision.
• Thorough understanding of GMP and pharmaceutical manufacturing.
• Strong leadership and communication skills.
• Willing to work on-site in Paarl, Western Cape.

Responsibilities

• Supervise daily production activities to meet schedules and quality objectives.
• Lead and train a team of production operators.
• Ensure GMP compliance and safety regulations.
• Monitor processes, identify issues, implement corrective actions.
• Optimize use of raw materials and equipment to minimize waste.
• Maintain production records and batch manufacturing records.
• Support process validation and quality initiatives.
• Conduct safety inspections and enforce procedures.
• Collaborate with R&D, QA, and Maintenance to resolve issues.
• Drive continuous improvement projects for efficiency and quality.

Skills

Team Leadership

GMP Compliance

Process Troubleshooting

Education

Bachelor's in Chemical Engineering/ Chemistry/ Pharmacy

Job description

About the Role

Our client, a growing pharmaceutical ingredient manufacturer, is seeking a dedicated Production Supervisor for their facility in Paarl, Western Cape . This role is responsible for overseeing daily production operations, ensuring that manufacturing targets are met efficiently and in compliance with stringent pharmaceutical quality standards (e.g., GMP). You will lead a team of production operators, providing guidance, training, and motivation to maintain high levels of productivity and product quality. The position requires a strong understanding of chemical manufacturing processes, particularly within the pharmaceutical sector, and excellent leadership skills. You will play a critical role in troubleshooting production issues, implementing process improvements, and ensuring a safe working environment. The ideal candidate is detail-oriented, organized, and committed to upholding the highest standards of quality and safety in a critical industry. Your leadership will directly impact the consistent supply of vital pharmaceutical compounds.

Key Responsibilities

• Supervise and coordinate daily production activities to meet manufacturing schedules and quality objectives.
• Lead, train, and motivate a team of production operators, fostering a positive and productive work environment.
• Ensure strict adherence to Good Manufacturing Practices (GMP) and all relevant safety and environmental regulations.
• Monitor production processes, identify potential issues, and implement corrective actions to maintain product quality and yield.
• Oversee the efficient use of raw materials and equipment, minimizing waste and downtime.
• Maintain accurate production records, batch manufacturing records (BMRs), and performance logs.
• Participate in process validation activities and support quality assurance initiatives.
• Conduct regular safety inspections and ensure all personnel follow safety procedures.
• Collaborate with R&D, Quality Control, and Maintenance departments to resolve operational challenges.
• Contribute to continuous improvement projects aimed at enhancing production efficiency and product quality.

Requirements

• Bachelor's degree in Chemical Engineering, Chemistry, Pharmacy, or a related scientific discipline.
• Minimum of 5 years of experience in chemical production, with at least 2 years in a supervisory or team lead role, preferably in the pharmaceutical or fine chemical industry.
• Thorough understanding of GMP requirements and pharmaceutical manufacturing processes.
• Strong knowledge of chemical batch processing and unit operations.
• Excellent leadership, team management, and communication skills.
• Proficiency in problem-solving and decision-making.
• Ability to interpret technical documents and manufacturing instructions.
• Commitment to safety and quality excellence.
• Must be willing to work on-site in Paarl, Western Cape .

Benefits

Our client offers a competitive salary, comprehensive health insurance, paid time off, and retirement benefits. We provide excellent opportunities for career advancement and professional development within the pharmaceutical sector. The company promotes a collaborative and supportive work culture. This position is based at our modern production facility in Paarl, Western Cape . Join a company committed to producing high-quality pharmaceutical ingredients.