Pharma Process Engineer - Lean, CI & Compliance

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

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