About the Role
Our client, a leading pharmaceutical manufacturer, is seeking a dedicated and highly skilled Chemical Engineer to join their state-of-the-art facility in Klerksdorp, North West. This role is essential for the development, optimization, and scale-up of chemical processes used in the production of active pharmaceutical ingredients (APIs) and drug formulations. You will work in a highly regulated environment, ensuring strict adherence to Good Manufacturing Practices (GMP) and quality standards. The position offers a fantastic opportunity to contribute to the development of life‑saving medicines and to advance your career within a respected organization known for its commitment to innovation and excellence. We are looking for a detail‑oriented engineer with a strong foundation in chemical engineering principles and a passion for the pharmaceutical industry.
Key Responsibilities
- Design, implement, and validate chemical processes for pharmaceutical manufacturing, ensuring GMP compliance.
- Optimize existing processes to improve yield, reduce cycle times, and enhance product quality.
- Conduct process hazard analyses (PHAs) and implement safety measures to ensure a safe working environment.
- Scale up laboratory processes to pilot and commercial production scales.
- Develop and execute process validation protocols and reports.
- Collaborate with Quality Assurance and Regulatory Affairs teams to ensure all activities meet stringent industry standards.
- Troubleshoot process deviations, identify root causes, and implement effective corrective actions.
- Prepare comprehensive technical documentation, including batch records, SOPs, and design reports.
- Stay current with industry trends, regulatory requirements, and new technologies in pharmaceutical manufacturing.
- Mentor junior engineers and technicians.
Requirements
- B.Sc. or M.Sc. in Chemical Engineering.
- Minimum of 5 years of experience in chemical engineering, with a strong focus on pharmaceutical or biotechnology process development and manufacturing.
- In-depth knowledge of GMP regulations and validation principles.
- Experience with process simulation and modeling software.
- Familiarity with chemical reaction engineering, crystallization, filtration, and drying processes.
- Excellent analytical, problem‑solving, and documentation skills.
- Strong communication and interpersonal skills to work effectively within multidisciplinary teams.
- Experience with aseptic processing is a plus.
- Must be legally eligible to work in South Africa and based in or willing to relocate to Klerksdorp, North West.
Benefits
- Competitive salary and benefits package, including medical aid and retirement fund.
- Opportunities for professional growth and advanced training in pharmaceutical sciences.
- Work in a modern, well‑equipped facility with cutting‑edge technology.
- Contribute to the development of impactful pharmaceutical products.
- Stable and secure employment in a growing industry.
- Supportive team environment in Klerksdorp, North West.