Senior Process Engineer - Pharmaceutical Manufacturing

About the Role

Our client is seeking a highly experienced Senior Process Engineer to enhance their pharmaceutical manufacturing operations in Reading . This vital role involves optimizing existing manufacturing processes and developing new ones to ensure efficiency, quality, and compliance with stringent industry standards. You will play a key part in troubleshooting production issues, implementing process improvements, and ensuring the successful scale-up of new products. The hybrid nature of this role allows for essential on-site process monitoring and engineering work, complemented by remote capabilities for data analysis, documentation, and strategic planning, ensuring maximum operational effectiveness.

Key Responsibilities

• Analyze manufacturing processes to identify areas for improvement in efficiency, yield, and cost-effectiveness.
• Lead process validation activities and ensure compliance with GMP and regulatory requirements.
• Develop and implement Standard Operating Procedures (SOPs) for new and existing manufacturing processes.
• Troubleshoot process deviations and implement corrective and preventative actions (CAPAs).
• Collaborate with R&D, Quality Assurance, and Production teams to ensure seamless product lifecycle management.

Requirements

• BEng or MEng in Chemical Engineering, Mechanical Engineering, or a related discipline.
• Minimum of 6 years of experience in process engineering within the pharmaceutical or biotechnology industry.
• Strong understanding of GMP, validation principles, and regulatory affairs.
• Proficiency in process simulation and data analysis software.
• Excellent problem-solving, communication, and project management skills.

Benefits

• Competitive salary and performance-related bonus scheme.
• Comprehensive private medical and dental insurance.
• Generous pension plan and life assurance.
• Opportunities for professional growth and advanced training.
• Hybrid work model supporting a balanced lifestyle.