Optimize pharmaceutical manufacturing processes in Kimberley with GMP expertise, validation knowledge, and process troubleshooting responsibilities. This hybrid role balances on-site involvement with off-site analysis.

The Process Engineer supports production of active pharmaceutical ingredients and finished dosage forms. You will improve yield, efficiency, and quality while supporting compliance with regulatory standards. The role includes process design, validation, documentation, and continuous improvement across manufacturing operations.

Key Responsibilities:

- Optimize processes for yield, efficiency, and product quality
- Develop SOPs, batch records, and validation protocols
- Troubleshoot production issues and implement effective solutions
- Participate in IQ, OQ,



and PQ validation activities
- Collaborate on current product introductions and improvements

Requirements:

- Bachelor's degree in Chemical Engineering or related science
- At least four years' pharmaceutical or biotechnology experience
- Strong GMP regulations and validation principles knowledge
- Experience with pharmaceutical unit operations
- Proficiency in process simulation and data analysis tools

Apply process engineering, GMP, validation, and analytical skills to improve pharmaceutical manufacturing performance in Kimberley.

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📌 Pharmaceutical Process Engineer GMP (Kimberley)
🏢 Placements24
📍 Kimberley