Medical Devices engineer jobs
- Freudenberg Performance Materials LP (United...Ebbw Vale
- Company pension
- You will support our team as Senior Development Engineer, to be responsible for leading site projects utilising project management techniques to develop and…
- Bragg Life SciencesMaldon
- Sick pay
- Relocation assistance
- Life insurance
- Free parking
- Company pension
- Private medical insurance
- They are looking to expand the R&D team by adding a Senior Design Engineer to work on a business critical project focusing on refrigeration systems and…
View similar jobs with this employerSThreeBirmingham- These positions centre on ensuring that sophisticated medical devices meet rigorous regulatory standards through comprehensive testing and validation protocols…
- Reactive RecruitmentLisburn
- Annual leave
- We’re recruiting a Manufacturing Engineer for a medical device manufacturer to help launch new products and improve production.
- Xstrahl LtdWalsall WS8 7DG
- The engineer must be able to communicate clearly and confidently, technical aspects of their work to physicists, scientists, and medical specialists.
- HR Smith GroupHereford HR2 6JZ
- Life insurance
- Free parking
- Company pension
- On-site parking
- Casual dress
- Company events
- An understanding of medical device quality systems, particularly ISO 13485, would be advantageous.
- Are you an engineer or technical specialist who enjoys…
- Corin GroupCirencester
- Referral programme
- Company pension
- Private medical insurance
- Free flu jabs
- Several years experience in Medical device design in medical devices, orthopaedics, or other regulated industries.
- 25 days holiday plus bank holidays.
- Strain Measurement Devices LtdBury St. Edmunds IP29 4UQ
- Company pension
- On-site parking
- Experience in a regulated or high-tech manufacturing environment, preferably involving sensors, electronics, medical devices, semiconductors, thin-film…
- Strain Measurement Devices LtdBury St. Edmunds IP29 4UQ
- Company pension
- On-site parking
- Experience in a regulated or high-tech manufacturing environment, preferably involving sensors, electronics, medical devices, semiconductors, thin-film…
- Corin GroupCirencester GL7 1YJ
- Referral programme
- Company pension
- Private medical insurance
- Free flu jabs
- Support a global portfolio of medical devices, including orthopaedic implants, reusable instruments, and single-use devices.
- 25 days holiday plus bank holidays.
- System Validation Engineers in medical device settings could play a critical role in ensuring that Class III devices meet rigorous regulatory standards before…
- Experience with Class III medical devices or comparable regulated product development.
- Roles of this type may sit within a collaborative quality and engineering…
- Xstrahl LtdWalsall WS8
- Employee assistance programme
- This role will support existing and new product activities, contributing to the electrical and electronic design and development.
- Domain: Class III medical device · Validation and quality assurance.
- Involvement in validating medical device systems that support patient safety and clinical…
View similar jobs with this employerMedequip Assistive Technology LtdNorwich NR6 6AQ- As the Specialist Engineer for Medequip Assistive Technology Ltd you will be responsible for assessing, servicing, repairing, and maintaining a range of…
View similar jobs with this employerSThreeBirmingham- Involvement in bringing Class III devices through to commercial release.
- This is an opportunity to register your interest in future Validation Engineer…
Job Post Details
Senior Development Engineer
Senior Development Engineer
Job details
Full job description
Working at Freudenberg: "We will wow your world!" This is our promise. As a global technology group, we not only make the world cleaner, healthier and more comfortable, but also offer our 52,000 employees a networked and diverse environment where everyone can thrive individually. Be surprised and experience your own wow moments. Freudenberg Performance Materials is part of the Freudenberg Group and a leading global supplier of innovative technical textiles for a broad range of markets: From apparel, automotive, building materials, civil engineering, energy, filter media, healthcare and to building interiors and more. Join our team and shape the future of innovation with us! Discover our world at www.freudenberg-pm.com.
You will support our team as Senior Development Engineer, to be responsible for leading site projects utilising project management techniques to develop and improve products and processes.
Senior Development Engineer
Responsibilities
- You will lead and deliver R&D projects, overseeing the design and development of new materials and the optimisation of manufacturing processes through laboratory and production-scale trials.
- You will organise and manage business continuity projects, including the dual sourcing of key raw materials, by coordinating activities with internal stakeholders, customers, and suppliers.
- You will partner with cross-functional teams to drive site improvement initiatives, leading and supporting projects focused on process enhancement, operational efficiency, and the introduction of new equipment.
- You will prepare and approve documentation supporting design control and validation activities, ensuring compliance with ISO 13485, customer requirements, and internal stage-gate processes (e.g., CIC).
- You will provide technical leadership and project management support to team members, departments, and sites, ensuring activities align with the FPM strategy and are supported by appropriate project documentation.
- You will act as a mentor to new team members, including placement students, providing guidance and support on project delivery and professional development.
- You will identify and champion new opportunities through technological awareness (e.g. literature and patent reviews) and market insights gained from trade shows, conferences, supplier engagements, and customer visits, translating these into innovative product and process development opportunities.
- You will ensure all R&D documentation, including work instructions and forms, is regularly reviewed, maintained, and improved in compliance with internal procedures, ISO standards, and industry best practices.
- You will support the planning, prioritisation, and scheduling of laboratory and manufacturing trials across all site R&D projects.
- You will manage the site Quentic COSHH system, ensuring chemical records, risk assessments, and associated documentation are maintained, compliant, and up to date, while providing support to system users across the site.
- You will complete routine project administration activities for assigned projects, including product costing and the creation and maintenance of product data within SAP and QPDC.
Qualifications
- Degree in Chemistry, Chemical Engineering or Polymer Science
- A minimum of 5 years of industrial experience of technical product development and project management
- Project Management certification e.g. Prince 2, Agile
- Lean Systems Green Belt or equivalent Lean/OPEX certification
- Have an understanding of HSE and chemical safety regulation (COSHH, COMAH, REACH)
- Have an understanding of project management methods (Prince 2, Agile)
- Have an understanding of ISO 13485 Medical Device Standard and Regulatory Requirements
- Demonstrated working knowledge of Operational Excellence (OPEX) tools
- Have experience of working in a laboratory environment
- You will have a good IT knowledge including Microsoft Office
- You will have/ develop a deep technical knowledge of PU foam raw materials and manufacturing processes
Some of your Benefits
Company Pension
Diversity & Inclusion
We focus on providing an inclusive environment and recognize our diversity contributes to our success.
Performance Related Bonus
When you have an impact, you can reap the rewards.
Workwear
For your safety and well-being we provide the proper clothing and equipment.
Personal Development
We offer a variety of trainings to ensure you can develop in your career.
The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.