Process Engineer (Braunton, GB, EX33 2DL)

Biopharma Careers; Braunton; On-site; GBP 40,000 - 60,000; Full time

Job summary

Biopharma Careers seeks a Process Engineer for our Braunton site to design, implement and optimise production processes for oral solid dose products. You will help ensure manufacturing operations are safe, compliant, and cost-effective, driving continuous improvements in a highly regulated environment.

In this role you will work with Maintenance, Production, Quality and Capital Projects to implement changes, perform technical reporting, and contribute to engineering documentation and SOP

Qualifications

• 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.

Responsibilities

• Design, implement and optimise processes used in production of pharmaceutical oral solid dose products.
• Contribute to pre-liminary financial analysis of improvements to quantify benefit.
• Evaluate potential improvements and oversee implementation of changes.
• Ensure processes meet EHS, Quality and regulatory requirements.
• Work with Maintenance, Production, Quality and Capital Project teams to design, implement and maintain equipment and systems.
• Apply Lean and Six Sigma to enhance efficiency and reduce waste.
• Contribute to Engineering Documentation, SOPs, validation protocols and user requirement specifications.

Skills

Lean Six Sigma

Process optimisation

Technical reports

cGMP

Education

Engineering degree

Job description

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.

Scope of the Role

Process Subject Matter Expert:

Achieveandmaintainexpertprocess and equipmentknowledgewithina specific area ofmanufacturing

Process Design and Optimisation:

Identifyopportunities 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

Regulatory Compliance:

Ensure processes meetEHS, Quality and other regulatory requirements

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

Production Support:

Work withMaintenance,Production, Quality andCapitalProject teamsto design, implementandmaintainproduction 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 EngineeringDocumentation/Drawing managementsystem

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