R&D Medical Device Design jobs
- EmbectaDún Laoghaire, County Dublin
- Experience with ISO standards, GMP guidelines, FDA regulations, medical device design controls, and manufacturing scale‑up processes.
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- Integer Holdings CorporationGalway, County GalwayAd
- This position provides product design & engineering support for new or existing catheter and guidewire products.
- As per skills & Knowledge section.
- AlconCork, County Cork
- Assist R&D Engineering in the specification, design and procurement of new equipment.
- The main responsibility is to support and drive R&D Engineering activities…
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R&D Engineer
NewJ&JGalway, County GalwayAd- A minimum of 2 years’ experience in all stages of medical device design and development (including design with SolidWorks, prototyping, testing).
- BDWexford, County Wexford
- Supports sustaining activities for existing medical devices.
- Participates and leads cross-functional teams in the design changes of a medical device and…
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View similar jobs with this employerLuminate MedicalGalway, County Galway- Previous experience working on the design of a new product that received medical device regulatory approval.
- Building prototypes to validate design concepts.
- ViatrisNorthern Cross, County Dublin
- Experience in quality management, ideally in the medical device industry or another regulated environment.
- Previous experience of Design Assurance in device…
View similar jobs with this employerICDS Recruitment ConsultantsSouth Dublin, County DublinAd- Process optimisation with strong background in design of experiments essential.
- High speed automation experience, test equipment fixture design and…
View similar jobs with this employerICDS Recruitment ConsultantsSouth Dublin, County DublinAd- Process optimisation with strong background in design of experiments essential.
- High speed automation experience, test equipment fixture design and…
View similar jobs with this employerICDS Recruitment ConsultantsSouth Dublin, County DublinAd- Process optimisation with strong background in design of experiments essential.
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- Abbott LaboratoriesGalway, County Galway
- Familiarity with medical device development processes and regulated environments is desirable.
- Analyse usability findings and support design recommendations.
- Cregg Recruitment LtdGalway, County GalwayAd
- Test design & interrogation and presentation of results for decisions.
- The successful candidate will lead end to end product design and concepts through NPI and…
- Cregg Recruitment LtdGalway, County GalwayAd
- Experience in materials selection and joining processes for medical devices.
- 3–7+ years’ experience in medical device R&D or product development preferred.
- MedtronicAthlone, County Westmeath
- Experience with disposable medical devices.
- This position is most suited for individuals with a broad background covering the total regulatory life cycle of…
- Boston ScientificClonmel, County Tipperary
- Experience with test method development, design verification, design validation, risk management, and design history file documentation.
Process & Product Development Engineer II for fixturing and tooling design (f/m/d)
Often replies in 1 dayTE ConnectivityGalway, County Galway- Employee stock purchase plan
- Wellness program
- Proven ability to conduct and contribute to FMEAs, verifications, and validations for medical device products and processes.
Job Post Details
Project Engineer R&D - job post
Job details
Job type
- Full-time
Location
Full job description
embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. For more information, visit embecta.com or follow our social channels on LinkedIn, Facebook, Instagram and X.
Why join us?
A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life’s purpose through the work that they do every day.
You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program – which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components – is designed to support the varying needs of our diverse and global employees.
The Project Engineer leads cross functional projects that support embecta’ s injection products portfolio. This role plays a key part in delivering projects that ensure regulatory compliance, support product changes, and enable business continuity and growth. The position offers the opportunity to manage initiatives that are critical to the long term success of the business.
About the Role
- Lead cross functional project teams delivering initiatives that impact compliance, form/fit/function, cost reduction, line extensions, and other business opportunities.
- Act as a primary liaison between business leadership, functional management, and project team members.
- Collaborate with functional managers to ensure appropriate resource allocation and discretionary spending to meet project timelines.
- Plan and facilitate regular project meetings to ensure all stakeholders are informed, aligned, and completing assigned actions.
- Work closely with Technical Subject Matter Experts (SMEs) to ensure all project tasks are clearly defined, planned, and executed.
- Assess the impact of change requests, including risks, costs, and schedule implications.
- Manage, and in some cases execute, engineering change deliverables through all stages of the Change Control process.
- Provide regular project status updates to senior management, covering quality, schedule, cost, and overall progress.
- Promote strong project planning, execution discipline, and rigor across all project activities to ensure successful outcomes.
What you bring
- Bachelor’s degree in an engineering or technology‑related discipline.
- Experience working in a regulated Medical Devices and/or Pharmaceutical industry environment
- Experience with product lifecycle management in high‑volume manufacturing environments.
- Solid understanding of structured product development processes, regulatory requirements, and quality systems.
- Experience with ISO standards, GMP guidelines, FDA regulations, medical device design controls, and manufacturing scale‑up processes.
- Excellent interpersonal and communication skills, with the ability to efficiently interact with diverse audiences and stakeholders
- Proven ability to work effectively both independently and as part of a cross‑functional team.
- Strong attention to detail and commitment to quality and compliance.
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embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.