Mechanical Plant Engineer

JR United Kingdom; Aberdeen City; On-site; GBP 35,000 - 55,000; Full time

Job summary

A global CDMO organization is seeking a Mechanical Plant Engineer to maintain mechanical systems and production equipment. This role includes preventive maintenance, troubleshooting, and collaborating on capital projects to ensure compliance with GMP standards. Ideal candidates will have a strong educational background in Mechanical Engineering and significant experience in a regulated environment.

Qualifications

• 3-5 years of mechanical maintenance experience in a regulated environment.
• Experience with pharmaceutical or biotech manufacturing equipment.

Responsibilities

• Maintain mechanical systems and equipment in compliance with GMP.
• Collaborate on capital projects and provide engineering expertise.
• Troubleshoot and implement solutions for mechanical issues.

Skills

Mechanical system diagnostics

Troubleshooting

GMP standards knowledge

Interpreting 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.