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Placements24 is seeking a Process Development Engineer for our Mossel Bay, Western Cape-based client in the biopharmaceutical sector. The role focuses on optimizing and scaling manufacturing processes while ensuring product quality and robust process controls.
The ideal candidate has a chemical/process engineering background with 4+ years in pharma manufacturing, and strong data-driven problem-solving abilities for cross-functional teams.
Our client, a prominent player in the biopharmaceutical sector, is looking for a dedicated Process Development Engineer to join their innovative team based in Mossel Bay, Western Cape . This role is integral to optimizing and scaling up manufacturing processes for our diverse range of pharmaceutical products. You will leverage your engineering expertise to improve efficiency, ensure product quality, and implement robust process controls. The ideal candidate has a strong foundation in chemical or process engineering, coupled with experience in pharmaceutical manufacturing environments. This is an exciting opportunity to contribute to the advancement of manufacturing technologies within a company that prioritizes innovation and operational excellence in Mossel Bay, Western Cape .
Design, develop, and optimize manufacturing processes for pharmaceutical products, ensuring efficiency, scalability, and compliance. Conduct process validation studies and author associated documentation. Implement and monitor process control strategies to ensure consistent product quality and yield. Troubleshoot and resolve process-related issues, identifying root causes and implementing corrective actions. Collaborate with R&D, Quality Assurance, and Manufacturing teams to ensure seamless technology transfer and process implementation. Develop Standard Operating Procedures (SOPs) and provide training to manufacturing personnel. Evaluate and implement new process technologies and equipment to enhance manufacturing capabilities. Analyze process data to identify areas for improvement and cost reduction. Ensure all process development activities comply with cGMP, safety regulations, and environmental standards.
Bachelor's degree in Chemical Engineering, Process Engineering, Mechanical Engineering, or a related field. Minimum of 4 years of experience in process development or manufacturing within the pharmaceutical or biopharmaceutical industry. Proven experience with process scale-up, validation, and troubleshooting. Solid understanding of cGMP principles and regulatory requirements. Familiarity with process analytical technology (PAT) and continuous manufacturing concepts is a plus. Strong analytical and problem-solving skills, with a data-driven approach. Excellent communication and interpersonal skills, with the ability to work effectively in cross-functional teams. Proficiency in process simulation software and statistical analysis tools.