Responsible for providing technical support across manufacturing and engineering operations to ensure efficient production performance, system compliance, and high-quality manufacturing standards. Supports process optimisation, control systems, continuous improvement, and technology transfer activities within a regulated environment.
Key Responsibilities
- Support DCS and process control systems to ensure performance, compliance, and data integrity.
- Troubleshoot process equipment and implement sustainable technical solutions.
- Manage CAPA activities and ensure timely execution and closure.
- Drive process optimisation, cost reduction, and energy efficiency initiatives.
- Lead Lean Six Sigma continuous improvement activities and performance reporting.
- Support technology transfer, commissioning, and startup of new systems and processes.
- Ensure compliance with cGMP, ISO, H&S, EMAS, and environmental requirements.
- Support validation, instrumentation, filtration, and purification activities.
Required Qualifications
- Bachelor’s degree in Chemical, Biochemical, or related Engineering discipline, or equivalent experience.
- Experience in process engineering within regulated manufacturing environments.
- Technical knowledge of control systems, validation, instrumentation, filtration, and purification processes.
- Proven ability to independently manage projects and technical engineering activities.
- Lean Six Sigma Yellow Belt or equivalent analytical/problem-solving capability.
Preferred Qualifications
- Experience within pharmaceutical or drug manufacturing operations.
- Experience in cGMP startup environments.
- Familiarity with DCS and PLC systems.
Work Environment
- Highly technical manufacturing environment focused on compliance, operational reliability, continuous improvement, and process optimisation.
