Chemical Engineer - Pharmaceutical Manufacturing

About the Role

Our client is seeking a skilled Chemical Engineer to contribute to their state-of-the-art pharmaceutical manufacturing facility in Plymouth, Devon . This role is focused on the process development, scale-up, and optimization of drug substance manufacturing. You will ensure that all processes meet stringent regulatory requirements (e.g., GMP) and contribute to the efficient production of life-saving medicines. This is a significant opportunity to advance your career in a highly regulated and impactful industry, working within a dedicated team committed to quality and innovation in Plymouth .

Key Responsibilities

• Develop and optimize chemical synthesis and purification processes for pharmaceutical intermediates and APIs.
• Lead technology transfer activities from lab scale to pilot and commercial manufacturing.
• Ensure all processes comply with Good Manufacturing Practices (GMP) and regulatory guidelines.
• Conduct process validation studies and prepare associated documentation.
• Troubleshoot and resolve complex process issues encountered during manufacturing.
• Collaborate with cross-functional teams including R&D, QC, and QA.

Requirements

• Degree in Chemical Engineering or a related scientific field.
• Minimum of 6 years of experience in pharmaceutical process development and manufacturing.
• Strong understanding of GMP, FDA, and EMA regulatory requirements.
• Experience with process scale-up, validation, and tech transfer.
• Proficiency in process modeling and data analysis tools.
• Excellent problem-solving skills and attention to detail.

Benefits

• Competitive salary and annual bonus.
• Comprehensive health, dental, and vision benefits.
• Pension plan with generous employer contributions.
• Generous paid time off and holiday allowance.
• Opportunities for professional development and international conferences in Plymouth .