Job title: Senior R&D Engineer
Location: Parkmore Business Park, Galway (Hybrid working)
Benefits: Excellent salary, 10% bonus, Hybrid working, Full family healthcare and pension contribution


Company:
My client are a rapidly growing medical device company offering a highly differentiated solution in SFA interventions. Their culture of innovation helps each individual develop both professionally and personally, their culture of respect means that they all work in a collaborative, empowering, and exciting environment.



Role:
Responsible for the co-ordination, development and design of new products and the co-ordination of resources as delegated by the R&D Technical Director and to complete assigned work in a manner which complies with the standards and procedures to which the company adheres.



Job Requirements:

• To perform project tasks as delegated by the relevant manager in adherence to the company’s procedures which have been developed in compliance with ISO13485, the Medical Device Directives/Regulations and FDA 21 CFR 820.
• To manage and co-ordinate assigned procedures, protocols, reports and purchases relevant to the R&D tasks and deliverables.
• To propose and lead the technical assessment of new product design inputs, collaborating closely and effectively with the cross-functional team, delivering high quality, original and elegant solutions to meet physician and patient needs.
• To provide design, development and technical input to the Company’s development projects.
• To ensure that other project team members are aware of their role and function within that team and to communicate the results and findings of relevant work to the team in a clear and comprehensible manner.
• Coordination of resources assigned by the relevant manager(s) to complete designated tasks.
• Mentors and trains junior staff or acts as a resource for colleagues with less experience.
• Cooperate with the QA and Design Assurance Department in developing test, verification and validation (including design review) procedures.

• Degree level qualification in engineering or a strongly related field.
• Professional Project Management certification desirable.

• A minimum of 5 experience in the area of medical devices, ideally within R&D/Product Development.
• Strong communication skills both written and verbal.
• Excellent organisational and time management skills with the ability to prioritise workload and work to tight deadlines.
• Exceptional attention to detail.