Mechanical Plant Engineer

JR United Kingdom; Wakefield; On-site; GBP 40,000 - 55,000; Full time

Job summary

A global CDMO organization in the UK is seeking a Mechanical Plant Engineer. The successful candidate will be responsible for maintaining mechanical systems, ensuring compliance with GMP standards, and supporting process improvements across the organization. Ideal candidates will have a degree in Mechanical Engineering and at least 3-5 years of relevant experience in a regulated environment.

Qualifications

• Minimum of 3–5 years of mechanical maintenance experience in a regulated environment.
• Proven experience with mechanical system diagnostics and maintenance in pharma or biotech.
• Proficient in reviewing and interpreting engineering drawings.

Responsibilities

• Perform preventive, predictive, and corrective maintenance on mechanical systems.
• Troubleshoot mechanical issues and implement effective solutions.
• Collaborate on capital and investment projects.

Skills

Mechanical system diagnostics

Troubleshooting

GMP standards knowledge

Reviewing engineering drawings

Automation systems understanding

Education

Bachelor's degree in Mechanical Engineering or related discipline

Job description

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Randstad Sourceright, a leading provider of RPO & MSP Recruitment Services are currently recruiting for an Mechanical Plant Engineer on behalf of a global CDMO organization.

The successful candidate will be responsible for maintaining mechanical systems and production equipment in accordance with GMP standards, while also contributing to capital investment projects and process improvements.

Key accountabilities:

• Perform preventive, predictive, and corrective maintenance on mechanical systems and pharmaceutical production equipment including chemical reactors, centrifuges, dryers and HVAC systems.
• Troubleshoot mechanical issues to root cause and implement effective, permanent solutions in compliance with safety and GMP regulations.
• Collaborate on capital and investment projects by providing mechanical engineering expertise, reviewing equipment specifications, layouts, and utility requirements.
• Participate in the review and verification of technical documentation including P&IDs, equipment drawings, datasheets, installation qualifications (IQ), and design documents to ensure compliance with cGMP and site standards.
• Maintain detailed maintenance logs and ensure all documentation is accurate, timely, and compliant with cGMP standards.
• Work closely with cross-functional teams (Production, Quality Assurance, Validation, and Engineering) to support equipment qualification, validation activities, and process improvements.

Key requirements:

• Bachelor's degree in Mechanical Engineering, Industrial Engineering, or related discipline (or equivalent technical qualification).
• Minimum of 3–5 years of mechanical maintenance experience in a regulated pharmaceutical, biotech, or CMO manufacturing environment.
• Proven experience with mechanical system diagnostics, troubleshooting, and equipment maintenance.
• Strong knowledge of GMP standards, chemical equipment, and facility systems (e.g., WFI, HVAC, clean steam, compressed air).
• Proficient in reviewing and interpreting engineering drawings, P&IDs, and technical documentation.
• Experience in GMP manufacturing environments.
• Understanding of automation systems and basic instrumentation
• Must be available for occasional weekend or after-hours support.