Process Engineer
Job in
Braunton, Barnstaple, Devon, EX31, England, UK
Listed on 2026-09-07
Listing for:
Perrigo
Full Time
position Listed on 2026-09-07
Job specializations:
-
Engineering
Process Engineer, Manufacturing Engineer, Quality Engineering -
Manufacturing / Production
Manufacturing Engineer, Quality Engineering
Job Description & How to Apply Below
Description Overview Description Overview We are excited to be recruiting for a Process Engineer to join our Process Engineering Team based in our Braunton manufacturing site.
This position will suit an engineering professional who is seeking a new challenge and has the technical capability, ingenuity and drive to make a difference by identifying and implementing process improvements.
This position reports to the Process & Project Engineering this role you will be responsible for designing, implementing, and optimizing processes used in the production of pharmaceutical oral solid dose products. You will help ensure that manufacturing operations are efficient, safe, cost-effective and compliant with regulatory standards.
Scope of the Role Process Subject Matter Expert:
Achieve and maintain expert process and equipment knowledge within a specific area of manufacturing Process Design and Optimisation:
Identify opportunities for process optimisation
Design process changes to realise the identified opportunities
Conduct engineering change management activities to assess proposed process changes
Contribute to pre-liminary financial analysis of improvements to quantify benefit
Evaluate potential improvements to ensure the most beneficial are prioritized
Oversee implementation of changes Regulatory Compliance:
Ensure processes meet EHS, Quality and other regulatory requirements
Conduct process and equipment assessments to identify risks and implement corrective actions Production Support:
Work with Maintenance, Production, Quality and Capital Project teams to design, implement and maintain production equipment and systems
Investigate and troubleshoot production issues and implement corrective actions Continuous Improvement:
Apply Lean and Six Sigma principles to enhance efficiency and reduce waste Documentation:
Contribute to the Engineering Documentation/Drawing management system
Contribute to the development of SOPs, validation protocols and user requirement specification
Write technical reports Experience Required Degree in a relevant engineering discipline required 3+ years of experience in a Process Engineering related role within a manufacturing environment required Experience working in an oral solid dose pharmaceutical manufacturing environment preferred
Experience with process optimisation required Experience writing technical reports required Experience working in a highly regulated industry preferred
Experience with industrial building services preferred Experience working in a cGMP environment preferred
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