Project Engineer

Maclivaro Limited; Leeds; On-site; GBP 40,000 - 60,000; Full time

Job summary

A global medical device manufacturer seeks a detail-oriented Project Engineer for a 12-month contract in Leeds. This hands-on role is pivotal in a regulated environment, ensuring compliance and driving engineering projects with a focus on quality and detail. Ideal candidates will possess solid GxP experience, excellent documentation skills, and a relevant engineering degree. If you value quality and impact, apply to be part of a meaningful initiative.

Qualifications

• Solid hands-on experience in a GxP-regulated environment.
• Proven track record of excellent document writing skills.
• Experience working within medical devices or similarly regulated industries.

Responsibilities

• Driving engineering projects within a highly regulated GxP environment.
• Owning and producing clear validation and technical documentation.
• Supporting and executing validation activities across equipment and processes.

Skills

Hands-on experience in a GxP-regulated environment

Excellent document writing skills

Strong understanding of validation

Education

Degree in Engineering (Mechanical, Electrical, Manufacturing, Systems)

Job description

Project Engineer – 12-Month Contract- Medical Devices

On-site | Leeds

A global medical device manufacturer is seeking a driven and detail-obsessed Project Engineer to join their Leeds site on a 12-month contract. This is a hands‑on role at the heart of a regulated manufacturing environment, ideal for someone who thrives in GxP settings, takes pride in flawless documentation, and enjoys turning complex engineering challenges into compliant, real‑world solutions.

If you like being close to the product, close to the process, and trusted to deliver, this role offers real impact from day one.

What You’ll Be Doing

• Driving engineering projects within a highly regulated GxP environment
• Owning and producing clear, robust validation and technical documentation
• Supporting and executing validation activities across equipment, processes, and changes
• Partnering closely with Quality, Manufacturing, and Engineering teams on site
• Ensuring every project meets the highest standards of compliance, safety, and performance

What We’re Looking For

• Solid, hands‑on experience in a GxP‑regulated environment (non‑negotiable)
• A proven track record of excellent document writing — protocols, reports, and change documentation
• Degree‑qualified in Engineering (Mechanical, Electrical, Manufacturing, Systems)
• or equivalent industry experience within regulated manufacturing
• Experience working within medical devices or similarly regulated industries
• Strong understanding and practical experience of validation

Nice to Have

• Exposure to CNC machining or CNC‑based manufacturing environments
• Experience working directly on the shop floor, not just from behind a desk

The Details

• Contract : 12 months
• Location : Fully on‑site, Leeds
• Environment : Fast‑paced, quality‑driven, and technically engaging

If you’re a Project Engineer who values quality, precision, and impact, we’d love to hear from you. Apply now to be part of something that truly matters.