CREGG is seeking an experienced Principal R&D Engineer to join our Galway-based client.
The successful candidate will lead the technical architecture and development of regulated device and general wellness-based products from concept through commercialization.
This role owns product specifications, technical feasibility, design integrity, and external engineering coordination.
Responsibilities
Technical Architecture & Product Specification Ownership
Define and author Product Requirement Documents (PRD), User Requirement Specifications (URS), and Technical Specifications
Establish system architecture for electromechanical and general wellness-based products
Ensure traceability between design inputs, outputs, verification plans, and risk documentation
Approve final product specifications prior to design freeze
Design Control & Risk Management
Lead design risk analysis (DFMEA, PHA)
Define verification and validation strategy
Ensure compliance with design control requirements
Support regulatory submissions through technical documentation preparation
External Engineering & Consultant Management
Act as our client's technical authority in engagements with mechanical, firmware, electrical, industrial design, and testing consultants
Define scope of work and performance expectations
Review and approve drawings, firmware specifications, test reports, and technical deliverables
Escalate technical risks or scope deviations
Qualifications and Experience
Minimum of Bachelor's Degree in Engineering, Material Science, or equivalent
6+ years R&D/NPD experience in relevant industry, preferably medical device or other comparable industry (Electronics, Mechanical, Automotive, etc.)
Knowledge of engineering theories, methods and work measurement techniques
Knowledge of design principles, FMEA, project management, regulatory requirements and standards, test development
Ability to mentor and coach assigned employees
Experience in electromechanical devices an advantage
Demonstrated ability to balance compliance and commercial reality
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