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- Join an exciting well established Medical Device company based in Cambridge
- Build and develop the QMS to new standards for the company
About Our Client
My client has been manufacturing precision optical and electromechanical equipment and instrumentation. My client is a leader in the development of precision motion, automation, and optical systems, sub-systems, and components and has been for over 100 years.
Job Description
- To act as the company Quality manager and also Health & Safety and Environmental manager
- To be part of the Operational Management Team running the day-to-day operations
- To ensure that quality, health & safety and environmental procedures and standards are enforced and worked to at all times by all staff
- To ensure that the company is kept up to date with all relevant legislation and best practice in the areas of Quality, H&S and Environmental issues.
- Ensure all training relevant to HSE requirements takes place and that deadlines are met for new requirements and the renewal of qualifications.
- Maintain the company certification to ISO and other standards as required
- To manage and supervise the Quality Team
- To write and maintain the company's procedures in collaboration with the people working in the areas affected
- To audit the company against its own procedures and process instructions
- To represent the company in dealing with external bodies, suppliers and customers
- Lead / take part in customer or supplier audits, reporting, analysing and taking actions on results as required
- Managing Supplier Quality Agreements and ensuring these requirements are understood and met internally.
- To work towards reducing the company's carbon footprint and championing sustainable initiatives
- To report key performance indicators to the directors and plan and manage any actions arising as a result
- To work with all appropriate departments in the resolution of customer complaints / returns
- To be able to assess and give a decision on the quality of product being manufactured and/or components delivered
- To organise and lead the process of management review of the company's systems, procedures and results
- To check and assure compliance of both the company and product against legislation such as RoHS, Modern Slavery Act, REACH and other legal and ethical requirements as required by a countries laws.
- To carry out any other reasonable requests as deemed necessary by the management team.
The Successful Applicant
- Good experience in preparation for audits to ISO9001 and ISO13485
- Previous experience in a managerial capacity is beneficial
- Vast QMS Experience
- CAPAs, Change Controls, Non-conformance, Deviations
- Running ISO accreditation, someone who has previous experience adapting do different standards
- Implementation of ISO13485 is beneficial
- Previous experience managing compliance.
What's on Offer
This a a brilliant chance to adopt a number of key responsibilities which are not often included in the same position. My client is looking for someone manage, implement, develop and maintain a QMS which they get to improve. As Quality Manager you will be section head of the Quality team.
Contact
Alex Henman
Quote job ref
JN-042022-5584865
Phone number
+44 172 773 0105
Job summary
- Sector
- Life Sciences
- Subsector
- Medical
- Sector
- Healthcare / Pharmaceutical
- Location
- Cambridge
- Contract type
- Permanent
- Consultant name
- Alex Henman
- Consultant phone
- +44 172 773 0105
- Job reference
- JN-042022-5584865