Process Engineer

Overview

In this role you will lead product transfers and drive process development to enable successful product introductions. You will optimize manufacturing processes, uphold GMP and regulatory standards, and provide technical leadership to resolve issues and improve performance. You’ll manage priorities, train manufacturing teams, and maintain safety and compliance. This is a chance to impact product quality and patient safety within a collaborative, fast-paced environment. You will work as a key technical contact, shaping transfer strategies and delivering measurable improvements.

Pay / Benefits

• site performance bonus
• pension scheme matching up to 8%
• life assurance
• generous holiday entitlement with tenure-based increases
• training and development
• LinkedIn Learning access

Responsibilities

• Lead product transfers, process development, and validation to ensure successful introductions
• Develop process specifications, optimize manufacturing processes, and drive continuous improvement
• Provide technical expertise to resolve process issues and enhance operational performance
• Ensure equipment, processes, and documents meet GMP, regulatory, and quality standards
• Manage project priorities and resources to meet business objectives and timelines
• Maintain safety, risk assessment, and regulatory compliance focus
• Train and support manufacturing teams on new processes and ensure training compliance
• Act as a key client contact, delivering technical updates, reports, and stakeholder communication

Key requirements

• Experience in pharmaceutical manufacturing, product development, or life sciences
• Knowledge of oral solid dosage (OSD) formulation and manufacturing processes
• Understanding of process scale-up, technology transfer, and GMP environments

• project leadership
• communication with stakeholders
• problem-solving
• Design of Experiments (DoE) and statistical analysis (desirable)
• technology transfer and process development
• GMP and regulatory compliance

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