Pharmaceutical Manufacturing Engineer

Placements24; Polokwane; On-site; ZAR 420,000 - 640,000; Full time

Benefits offered by this job

Competitive salary

Health insurance

Retirement plan

Career growth

Modern facilities

Collaborative environment

Job summary

Placements24 is seeking an experienced Pharmaceutical Manufacturing Engineer to join thePolokwane-based operations team. You will optimize and maintain pharmaceutical manufacturing processes, ensure GMP compliance, and drive continuous improvement across production lines.

The role requires a strong engineering background, hands-on experience with process validation (IQ/OQ/PQ), and collaboration with QA, QC, and production to sustain high quality and efficiency in a regulated environment.

Qualifications

• Bachelor's degree in chemical or mechanical engineering.
• Minimum 4 years of process engineering/manufacturing experience in pharma.
• Solid understanding of pharma manufacturing processes and equipment.
• Experience with GMP and regulatory compliance in pharma.
• Experience with process validation (IQ/OQ/PQ) and commissioning.

Responsibilities

• Oversee operation, maintenance, and calibration of pharmaceutical manufacturing equipment.
• Implement process improvement projects to enhance efficiency, reduce waste, and improve product quality.
• Troubleshoot and resolve technical issues with manufacturing equipment and processes.
• Develop and execute validation protocols (IQ, OQ, PQ) for new or modified equipment and processes.
• Ensure GMP, safety regulations, and environmental standards are followed.
• Collaborate with production, quality control, and quality assurance teams to ensure seamless operations.

Skills

Problem solving

Analytical thinking

Engineering background

Education

Bachelor's degree in Chemical or Mechanical Engineering

Job description

About the Role

Our client is seeking a proactive and experienced Pharmaceutical Manufacturing Engineer to join their operational team in Polokwane. This role is essential for optimizing and maintaining the efficiency, quality, and safety of pharmaceutical manufacturing processes. You will be involved in process improvement initiatives, troubleshooting manufacturing equipment issues, and ensuring adherence to strict GMP regulations. The ideal candidate will have a strong engineering background, a thorough understanding of pharmaceutical production, and a commitment to continuous improvement within a regulated manufacturing environment.

Key Responsibilities

• Oversee the operation, maintenance, and calibration of pharmaceutical manufacturing equipment.
• Implement process improvement projects to enhance efficiency, reduce waste, and improve product quality.
• Troubleshoot and resolve technical issues with manufacturing equipment and processes.
• Develop and execute validation protocols (IQ, OQ, PQ) for new or modified equipment and processes.
• Ensure all manufacturing activities comply with GMP , safety regulations, and environmental standards.
• Collaborate with production, quality control, and quality assurance teams to ensure seamless operations.

Requirements

• Bachelor's degree in Chemical Engineering, Mechanical Engineering, or a related field.
• Minimum of 4 years of experience in process engineering or manufacturing within the pharmaceutical industry.
• Solid understanding of pharmaceutical manufacturing processes and equipment (e.g., reactors, filtration, drying, packaging).
• Experience with process validation, GMP, and regulatory compliance in a pharmaceutical setting.
• Strong problem-solving and analytical skills, with the ability to work under pressure.
• Proficiency in relevant engineering software and tools.

Benefits

• Competitive salary and potential for annual bonuses.
• Comprehensive health insurance and retirement savings plan.
• Opportunities for career advancement within the company.
• Access to modern manufacturing facilities and technology.
• A collaborative work environment focused on operational excellence.