Process Engineer; Braunton, GB, EXDL

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 Manager.

In 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.

Achieveandmaintainexpertprocess and equipmentknowledgewithina specific area of manufacturing

Identify opportunities forprocessoptimisation

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

Ensure processes meetEHS, Quality and other regulatory requirements

Conduct process and equipment assessments to identify risks and implement corrective actions

Work with Maintenance,Production, Quality and Capital

Project teamsto design, implementandmaintainproduction equipment and systems

Investigate and troubleshoot production issues and implement corrective actions

Apply Lean and Six Sigma principles to enhance efficiency and reduce waste

Contribute to the Engineering Documentation/Drawing management system

Contribute to the development of SOPs, validation protocols and user requirement specification

Write technical reports

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