Process Engineer

Perrigo Company; Braunton; On-site; GBP 45,000 - 65,000; Full time

Job summary

Perrigo Company in Braunton is recruiting a Process Engineer to join the Process Engineering Team. You will design, implement and optimise processes for oral solid dose pharmaceutical manufacturing, ensuring efficiency, safety, cost-effectiveness and regulatory compliance.

You will work with cross-functional teams to identify opportunities, manage changes and support production equipment and systems while applying Lean and Six Sigma to reduce waste and improve performance.

Qualifications

• Degree in an engineering discipline is required.
• Experience with process optimisation is essential.
• Experience writing technical reports is required.
• Experience in a highly regulated industry is preferred.

Responsibilities

• Achieve and maintain expert process and equipment knowledge within a manufacturing area.
• Identify opportunities for process optimisation and design changes to realise benefits.
• Conduct change management and preliminary financial analyses of improvements.
• Ensure regulatory compliance with EHS and Quality standards.
• Collaborate with Maintenance, Production, Quality and Capital Projects to support equipment and systems.
• Apply Lean and Six Sigma to drive efficiency and reduce waste.
• Contribute to engineering documentation, SOPs and validation protocols.

Skills

Process Engineering

Lean Six Sigma

Regulatory Compliance

Documentation

Continuous Improvement

Production Support

Education

Engineering degree

Job description

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:

• 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