Validation Project Engineer

Adepto Technical Recruitment Ltd; Leeds; On-site; GBP 80,000 - 100,000; Full time

Job summary

A recruitment agency is seeking a Validation Project Engineer for a 12-month contract in West Yorkshire. The role focuses on ensuring GxP compliance in medical device manufacturing and involves leading validation projects, creating detailed documentation, and collaborating with diverse teams. Candidates should have extensive GxP experience, excellent documentation skills, and a degree or relevant experience in engineering disciplines. This position offers a chance to contribute to advancements in healthcare technology.

Qualifications

• Extensive experience in GxP compliance is required.
• Exceptional skills in documentation are essential.
• Degree or substantial experience in medical devices or engineering needed.

Responsibilities

• Lead validation projects to ensure industry compliance.
• Craft detailed documentation to support validation.
• Collaborate with teams to ensure project success.

Skills

GxP experience

Document writing skills

Validation experience

Education

Degree in relevant engineering discipline

Tools

CNC systems knowledge

Job description

Validation Project Engineer - Medical Device

Are you a seasoned Validation Project Engineer with a passion for the medical device sector? A new project awaits in West Yorkshire, offering a 12‑month contract outside IR35. This position promises an enriching experience, working on cutting‑edge projects that make a real difference in healthcare.

The role centres around ensuring the highest standards of quality and compliance in medical device manufacturing. Your expertise will be pivotal in maintaining GxP (Good Practice) standards, a critical aspect of this position. This is an excellent chance to apply and further hone your skills in a dynamic and impactful environment.

Key Responsibilities

• Leading validation projects to ensure compliance with industry standards.
• Crafting detailed and precise documentation to support validation processes.
• Collaborating with cross‑functional teams to drive project success.

Required Qualifications

• Extensive GxP experience, a non‑negotiable requirement for this role.
• Exceptional document writing skills, essential for maintaining rigorous standards.
• A degree or substantial experience in medical devices or relevant engineering disciplines such as electrical, mechanical, systems, or manufacturing engineering.
• Proven validation experience, demonstrating a thorough understanding of validation processes and protocols.

While not mandatory, knowledge of CNC (Computer Numerical Control) systems will be highly regarded and could set you apart from other candidates.

This role is ideal for professionals seeking to leverage their expertise in a challenging and rewarding setting. The contract offers stability and the chance to contribute to significant advancements in medical technology.

Engage in a role that not only values your skills but also provides a platform for professional growth and development.