A vacancy has arisen for an experienced Senior Quality Engineer working within Renishaw Mayfield based in Chassieu, in Lyon region.
The successful candidate will be required to provide Quality Engineering support for Mayfield manufactured or subcontract manufactured current and development products, these include a robot used in neurosurgery and supporting devices.
Key tasks will include the review and/or generation of non-conformance reports, CAPA, audit, validation protocols/reports, risk management and design change documentation.
The successful candidate will be required to work closely with the team in Lyon, as well as across teams based in Gloucestershire (England) and Swords (Ireland).
The candidate will be required to be on-site a minimum of 3 days a week.
Main ResponsibilitiesWith the support of the QM, implement, maintain and control the Quality Management System and maintain its effectiveness
Prepare, organize and carry out internal and supplier audits
Support notified body audits, and lead on follow-up tasks from the audits
Line management of the Quality Technician
Review and approve CAPAs, non-conformances and complaints
Participate in projects as the quality representative, reviewing and approving associated documents
Provide training to staff on the procedures and instructions put in place
Prepare, organize and lead management reviews
Monitor Quality indicators related to the company's processes
Participate in post-market surveillance activities
Review DHR, inspection/build paperwork and release product
Daily support to operational teams especially for the handling of non-conforming products
Define and implement quality process improvements
Fostering the team’s quality mindset
Key Requirements:
4-6 years’ experience in a medical device Quality Engineering role
Detailed knowledge of ISO13485, ISO 14971 and 21CFR Part 820 Quality System Regulation (QSR) and MDSAP
Experience in nonconforming product management, CAPA, design change activities, risk and validation activities
Strong root cause analysis skills
Ability to write documents and speak fluently in French and English.
Travel to subsidiary sites and suppliers will be a requirement of the position.
Desirable requirements:
Life science, engineering, medically related degree or appropriate experience
Experience in neurological devices
Knowledge of Quality tools and statistics
Additional validation experience (process, equipment, cleaning, sterilisation, Test Method Validation)
Lead auditor trained for ISO 13485 / Internal auditor trained to ISO 13495 / MDSAP
NPI
6 sigma green belt or above
Experience in line managing
The successful applicant will be organised and self-motivated, possessing an eye for detail and excellent communication skills.
Embracing change is essential, as it allows the applicant to adapt and thrive in a dynamic environment.
As a team player, the applicant will be self-determined and have a strong voice for Quality, ensuring high standards are maintained.
Working to strict deadlines is crucial, and the applicant will encourage and facilitate others to do the same.
Finally, the ability to cope with pressured situations and to be flexible in working hours is an essential requirement of this role, ensuring the applicant can handle the demands of the position effectively.
Location: Chassieu, Lyon region
Salary: in accordance with experience and qualifications
Permanent and full-time contract
Laptop, mobile phone
Immediate incorporation
and additional benefits, such as:
- Discretionary annual bonus
- Training customized initiatives
- Long-term opportunities for professional development in an international company
- Referral program with paid compensation
- Online wellbeing benefits
- A collaborative and inclusive culture of sharing and teamwork
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At Renishaw we believe that our success is powered by welcoming a workforce of diverse and talented people. Through encouraging an inclusive culture, where all our employees are free to be themselves, we can achieve our core values: Innovation, Inspiration, Integrity, and Involvement. We believe in a culture of diversity to attract the best people, be part of the best environments and adapt to our diverse customers. We provide equal consideration for employment to all qualified applicants without regards to race, colour, religion, sex, gender identity, sexual orientation, experience, background, age, perspectives and abilities. Renishaw is an equal opportunity employer and is committed to provide any reasonable accommodation for differently abled candidates. Should you have any difficulty during the recruitment process, or require any reasonable adjustments please contact the recruitment team at [email protected]. Please click here for further information about diversity and inclusion at Renishaw.
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What We Do
Renishaw is one of the world's leading engineering and scientific technology companies, with expertise in precision measurement and healthcare. The company supplies products and services used in applications as diverse as jet engine and wind turbine manufacture, through to dentistry and brain surgery. It is also a world leader in the field of additive manufacturing (also referred to as 3D printing), where it designs and makes industrial machines which ‘print' parts from metal powder.
The Renishaw Group currently has 80 offices in 36 countries, with over 5,000 employees, of which over 3,000 people are employed within the UK. The majority of the company's R&D and manufacturing is carried out in the UK and for the year ended June 2019, Renishaw achieved sales of £574 million of which 94% was due to exports. The company's largest markets are USA, China, Japan and Germany









