CR
R&D Manager
Cpl Resources - Science & Engineering
Wexford · On-site Full-time Lead 1mo ago
About the role
Job Summary
We are partnering with a leading global organisation within the delivering innovative medical technologies across vascular, oncology, and renal care. They are seeking an experienced R&D Manager to lead new product development activities from concept through to commercialisation, managing cross-functional teams and driving innovation within a highly regulated environment. This is a key leadership role offering the opportunity to influence strategy, oversee product delivery, and contribute to meaningful advancements in medical device technology.
Responsibilities
- Lead and coordinate all aspects of product development across cross-functional teams including RA, QA, Operations, Clinical, Marketing, and Manufacturing
- Manage end-to-end project delivery, including timelines, budgets, and resource allocation
- Oversee design, development, and transfer to manufacturing of new medical device products
- Drive process development, including vendor selection, validation, and optimisation of manufacturing processes
- Review and approve technical documentation, validation protocols, and product development plans
- Ensure robust verification, validation, and testing strategies are implemented
- Mentor and lead R&D teams, providing coaching, performance management, and development support
- Manage departmental budgets and cost analysis, identifying opportunities for efficiency improvements
- Support cross-functional teams in ensuring compliance with regulatory and quality standards
- Contribute to root cause investigations, product improvements, and innovation initiatives
Requirements
- Bachelor’s degree in Mechanical, Biomedical, Chemical Engineering or related discipline (Biomedical preferred)
- 8+ years’ experience in R&D or process development, ideally within medical devices or a regulated industry (FDA/QSR/ISO)
- Proven experience in product development and manufacturing processes
- Strong knowledge of process validation (IQ, OQ, PQ) and verification/validation activities
- Demonstrated ability to lead cross-functional teams and manage complex projects
- Strong analytical mindset with experience using statistical tools/software
- Excellent communication and stakeholder management skills
- Six Sigma or Design for Six Sigma training is highly desirable
Benefits
- Family Healthcare Cover
- 9.75% employer pension contribution + 5% employee contribution
- Performance Bonus targeted at 8%
- Global Share Investment Program
- Life Assurance Cover
- 24 days annual leave + 10 public holidays
Skills
CommercializationDesign HistoryProcess DevelopmentProcess ValidationProduct DevelopmentProduct lifecycleR&D
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