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Product Development Specialist
2 weeks ago
We are seeking a highly skilled and experienced NPD Engineer to join our team in Longford. As an NPD Engineer, you will play a key role in the development of new medical products, working closely with cross-functional teams to design, develop, and launch innovative solutions.
Key Responsibilities:
- Design and develop new advanced wound care, ostomy, surgical/NPWT & skincare products
- Completion of design & development deliverables as per design & development planning process
- Co-ordination of internal testing reports, biocompatibility testing reports & technical file development
- Supporting product Bioburden, Bioburden validation & sterilisation validation activities during product development
- Prototyping of new products, internal reviews & external review for design freeze
- Supporting regular meetings with customers and internal functional groups for projects
- Generation & Maintenance of Product Design Files
- Management of new product introduction projects
- Material Research, Sourcing & Testing
- Responsible for the full co-ordination of trials from scheduling to line clearance post trial
- Product cost development with Finance
- Quality assurance reviews of R&D Documents
- Maintenance & improvement of the R&D Laboratory
- New process introductions, including identification of new equipment & test methods
- Participating in design reviews and the compilation of associated documentation
- Supporting product development validation planning, protocols and reports
- Generating Raw Material specifications, including artwork & label approvals as well as bill of Materials for new product developments and introductions
- Product, Packaging, Splice & Design Specification building during product development
We are looking for a candidate with a strong background in medical device development, preferably with experience in product design and R&D. The ideal candidate will have a degree in a science or engineering discipline, specializing in chemistry/physics/polymer fields, and excellent analytical and problem-solving skills.
The successful candidate will also have:
- 2-5 years' experience working in a medical device environment
- Working knowledge of ISO 13485 Design Control requirements
- Validation experience including sterilization, process, and packaging validations
- Excellent verbal communication skills
- Ability to work in a fast-paced dynamic environment
- Knowledge of medical device manufacturing environments, including GMP (Good Manufacturing Practice)
As a valued member of our team, you will receive a competitive salary and benefits package, including opportunities for professional growth and development.
This is a full-time, on-site position, and we do not offer remote working options.