Pharmaceutical Manufacturing Engineer

Placements24; Mbombela (Nelspruit); On-site; ZAR 700,000 - 950,000; Full time

Benefits offered by this job

Health insurance

Retirement plan

Life assurance

Paid time off

Professional development

Job summary

Placements24 is seeking a skilled Pharmaceutical Manufacturing Engineer for a state-of-the-art facility in Nelspruit (Mbombela). You will optimize manufacturing processes, maintain GMP compliance, and implement new technologies to improve yield, safety, and quality.

Strong problem-solving and project management skills are essential for cross-functional collaboration. Responsibilities include equipment installation, commissioning, validation, and CAPA-driven improvements, with emphasis on

Qualifications

• Bachelor's degree in Chemical or Mechanical Engineering or related field.
• Minimum 4 years in Pharmaceutical Manufacturing or Process Engineering.
• GMP knowledge and regulatory awareness is essential.

Responsibilities

• Design, develop, and optimize manufacturing processes and equipment to improve efficiency and quality.
• Troubleshoot production equipment and processes to resolve issues promptly.
• Lead projects including installation, commissioning, validation, and qualification.
• Ensure GMP, safety, and environmental standards across all activities.
• Develop and maintain process documentation, SOPs, batch records, and validation protocols.
• Collaborate with QA, Production, and R&D to support product lifecycle management.
• Perform root cause analysis for deviations and implement CAPAs.

Skills

Analytical skills

Problem-solving

Project management

Troubleshooting

Education

Bachelor's degree in Chemical Engineering or Mechanical Engineering

Tools

Process simulation software

CAD tools

Job description

Our client is looking for a skilled and innovative Pharmaceutical Manufacturing Engineer to join their state-of-the-art facility in Nelspruit . This role is central to optimizing and maintaining the efficiency, safety, and compliance of our pharmaceutical production processes. You will apply engineering principles to improve existing manufacturing lines, implement new technologies, and ensure that all operations adhere to stringent Good Manufacturing Practices (GMP). This position is perfect for an engineer passionate about advancing pharmaceutical production through technical expertise and problem-solving.

Key Responsibilities

• Design, develop, implement, and optimize manufacturing processes and equipment to enhance efficiency, yield, and product quality.
• Troubleshoot and resolve technical issues related to production equipment and processes.
• Lead engineering projects, including equipment installation, commissioning, validation, and qualification.
• Ensure all manufacturing activities comply with Good Manufacturing Practices (GMP) , safety regulations, and environmental standards.
• Develop and maintain process documentation, including SOPs, batch records, and validation protocols.
• Collaborate with Quality Assurance, Production, and R&D teams to support product development and lifecycle management.
• Conduct root cause analysis for manufacturing deviations and implement effective corrective and preventative actions (CAPAs).

Requirements

• Bachelor's degree in Chemical Engineering, Mechanical Engineering, or a related engineering discipline.
• Minimum of 4 years of experience in a Pharmaceutical Manufacturing or Process Engineering role.
• Strong understanding of GMP, pharmaceutical manufacturing principles, and regulatory requirements.
• Experience with process automation, validation (IQ/OQ/PQ), and troubleshooting of manufacturing equipment (e.g., reactors, filtration systems, packaging lines).
• Proficiency in process simulation software and CAD tools is a plus.
• Excellent analytical, problem-solving, and project management skills.

Benefits

• Competitive annual salary and performance-based bonus opportunities.
• Comprehensive health insurance, retirement plan, and life assurance.
• Generous paid time off and company holidays.
• Support for professional development, including continued education and engineering certifications.
• A collaborative and innovative work environment focused on producing high-quality medicines.