Senior Compliance Engineer
Northleach, Gloucestershire
£50,000 - £50,000/annum
Posted 2 days ago
About the role
Astor Bannermans Medical Device product line is continually evolving and growing. We require an experienced compliance engineer to help us navigate our regulatory requirements for new and existing products. If you want to be part of a company creating products that directly improve peoples lives, then this is a perfect opportunity.
Make sure to read the full description below, and please apply immediately if you are confident you meet all the requirements.
Requirements
Youll be a technically capable and detail orientated engineer with experience in medical device testing and certification, with a strong grasp of compliance standards.
A relevant degree i.e. Engineering (Elec eng. preferred), Medicine or another relevant scientific discipline or 6+ years experience in a compliance or regulatory affairs role.
Hands on experience in product testing and validation
Knowledge of regulatory requirements for Class I medical devices to MDD and MDR.
Experience and competence complying to ISO9001, ISO13485, ISO14971.
Experience testing and complying to IEC60601-1 and other parts (such as -2, -6, -11)
Strong analytical and documentation skills
Proactive, organised, self-starter & passionate about standards.
Confident communicator, able to work across function and to external agencies
Responsibilities:
Technical Content File creation, maintenance and ownership.
Support product classification levels of medical & machine products.
Plan, conduct and oversee all testing both internally and externally
Operate and maintain any testing equipment
Ensure compliance for the full product range, regularly updating where needed to UK, EU, USA and ROW.
Support Certification submissions and liaise with regulatory bodies and test houses.
Collect and analyse test data, providing detailed reports and recommendations
Carry out risk assessments and FMEAs to support safe and compliant design
Stay up to date on applicable standard and regulations
Drive improvements across R&D in test methods, documentation and compliance processes
Ensure documentation, drawings, labels, manuals, etc. are accurate and consistent.
Integrate best practice into the R&D engineering team
Our Company
We design, develop and manufacture paediatric medical equipment. Our products are primarily focused on washing, bathing, changing and handling solutions that directly improve peoples lives. We have been established for over 30 years but are now heavily investing in our future as we are expanding.
Why should you apply?
Competitive salary based on experience & flexible hours.
Working in a small, fun & dynamic R&D and Quality team.
Surrounded by the beautiful Cotswolds but close to Cheltenham (GL54).
Immediate start possible, on-site parking.
Healthcare scheme, bike to work & pension contribution. xwzovoh
Growing business where you can really make an impact on your career whilst improving other peoples wellbeing.
Make sure to read the full description below, and please apply immediately if you are confident you meet all the requirements.
Requirements
Youll be a technically capable and detail orientated engineer with experience in medical device testing and certification, with a strong grasp of compliance standards.
A relevant degree i.e. Engineering (Elec eng. preferred), Medicine or another relevant scientific discipline or 6+ years experience in a compliance or regulatory affairs role.
Hands on experience in product testing and validation
Knowledge of regulatory requirements for Class I medical devices to MDD and MDR.
Experience and competence complying to ISO9001, ISO13485, ISO14971.
Experience testing and complying to IEC60601-1 and other parts (such as -2, -6, -11)
Strong analytical and documentation skills
Proactive, organised, self-starter & passionate about standards.
Confident communicator, able to work across function and to external agencies
Responsibilities:
Technical Content File creation, maintenance and ownership.
Support product classification levels of medical & machine products.
Plan, conduct and oversee all testing both internally and externally
Operate and maintain any testing equipment
Ensure compliance for the full product range, regularly updating where needed to UK, EU, USA and ROW.
Support Certification submissions and liaise with regulatory bodies and test houses.
Collect and analyse test data, providing detailed reports and recommendations
Carry out risk assessments and FMEAs to support safe and compliant design
Stay up to date on applicable standard and regulations
Drive improvements across R&D in test methods, documentation and compliance processes
Ensure documentation, drawings, labels, manuals, etc. are accurate and consistent.
Integrate best practice into the R&D engineering team
Our Company
We design, develop and manufacture paediatric medical equipment. Our products are primarily focused on washing, bathing, changing and handling solutions that directly improve peoples lives. We have been established for over 30 years but are now heavily investing in our future as we are expanding.
Why should you apply?
Competitive salary based on experience & flexible hours.
Working in a small, fun & dynamic R&D and Quality team.
Surrounded by the beautiful Cotswolds but close to Cheltenham (GL54).
Immediate start possible, on-site parking.
Healthcare scheme, bike to work & pension contribution. xwzovoh
Growing business where you can really make an impact on your career whilst improving other peoples wellbeing.
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