Technical Documentation Engineer
- Recruiter
- Confidential
- Location
- Merseyside
- Salary
- 35000.00 - 45000.00 GBP Annual
- Posted
- 14 Sep 2021
- Closes
- 12 Oct 2021
- Sectors
- Engineering
- Contract Type
- Permanent
- Hours
- Full Time
Serve Talent have partnered with a successful manufacturing business to recruit a Technical Documentation Engineer for their site in Saint Helens, Merseyside. The business specialises in both the Medical Device & Food and Drug administration sectors.
Reporting into the Technical Manager and working alongside the wider Technical team, your main job will be to produce Technical Documentation whilst ensuring that the requirements of the file are met.
Responsibilities will include but not be limited to:
Completion of technical documentation.
Ensuring the requirements of the technical file for MDR/FDA are met.
Filing of new products for CE review and approval.
Updating an existing technical documents with new information.
Assist with CE audits.
Ideally you'll have:
A degree in an Engineering discipline, Physics or similar. Or you'll have the equivalent experience.
Experience of working in a Technical approvals function, ideally covering medical or electronics products.
Demonstrable experience in generating and submitting documentation.
Project management experience
This is a fantastic opportunity for a Technically focused person to take the next step in their career, by joining an established team of experienced Engineers and developing your career long term.
Alongside a competitive salary and benefits package, is a carved out career development plan with significant scope for promotion and development for those who want it.
If you have the skills and experience required and would like to be considered, apply now
Reporting into the Technical Manager and working alongside the wider Technical team, your main job will be to produce Technical Documentation whilst ensuring that the requirements of the file are met.
Responsibilities will include but not be limited to:
Completion of technical documentation.
Ensuring the requirements of the technical file for MDR/FDA are met.
Filing of new products for CE review and approval.
Updating an existing technical documents with new information.
Assist with CE audits.
Ideally you'll have:
A degree in an Engineering discipline, Physics or similar. Or you'll have the equivalent experience.
Experience of working in a Technical approvals function, ideally covering medical or electronics products.
Demonstrable experience in generating and submitting documentation.
Project management experience
This is a fantastic opportunity for a Technically focused person to take the next step in their career, by joining an established team of experienced Engineers and developing your career long term.
Alongside a competitive salary and benefits package, is a carved out career development plan with significant scope for promotion and development for those who want it.
If you have the skills and experience required and would like to be considered, apply now