Validation Project Engineer
Posted 1 day ago by Adepto Technical Recruitment Ltd
£60 Per hour
Outside
Undetermined
West Yorkshire
Summary: The Validation Project Engineer role focuses on ensuring quality and compliance in medical device manufacturing within a 12-month contract in West Yorkshire, outside IR35. The position involves leading validation projects, crafting documentation, and collaborating with teams to drive success. Candidates will apply their GxP expertise in a dynamic environment that contributes to advancements in healthcare technology.
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.
Key Skills:
- 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.
- Knowledge of CNC (Computer Numerical Control) systems is highly regarded.
Salary (Rate): £60/hour
City: West Yorkshire
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: outside IR35
Seniority Level: undetermined
Industry: Other
Validation Project Engineer - Medical Device
Are you a seasoned Validation Project Engineer with a passion for the medical device sector? A new projects 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 include:
- 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.
Candidates must possess:
- 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.