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Freudenberg

Senior Research & Development Engineer

LocationCarrick-on-Shannon, Co. Leitrim
Typefull-time
SenioritySenior
Experience4+ yrs
DepartmentEngineering
Company size10,000+ people
First seenOct 4, 2026 · 1w ago
Verified live1d ago
At a glanceSummarised by Seekless from the posting.
Must have14
Third-level qualification in Engineering or Science, preferably Mechanical or Biomedical; minimum Bachelor’s degree in Science, Technology, Engineering, or a related discipline (Mechanical, Manufacturing, Automation, or equivalent)
Proven design capability with CAD systems, ideally Solid Edge
Senior-level candidates should have a minimum of 4 years’ relevant experience
Excellent interpersonal and communication skills, with the ability to collaborate effectively across teams
Leads the design and development of complex medical devices from concept through to design freeze
Solves high-level engineering challenges using advanced materials knowledge, precision manufacturing methods, and data-driven decision making
Acts as a subject matter expert in catheter systems, extrusion-based assemblies, and biomaterials, influencing design direction and technical standards
Develops and executes verification and validation protocols (IQ/OQ/PQ), ensuring compliance with ISO 13485 and FDA 21 CFR Part 820
Manages cross-functional technical projects, balancing design intent, manufacturability, and regulatory requirements
Leads FMEA, risk analysis, and root cause investigations to ensure robust design and process outcomes
Provides technical mentoring and reviews for junior engineers and project teams, helping to build capability and ensure knowledge transfer
Drives innovation by exploring emerging technologies, novel components, and automation opportunities
Develops and maintains detailed documentation including DHFs, BOMs, drawings, and test reports in compliance with QMS requirements
Engages directly with customers to understand application needs, presenting technical solutions and leading design iterations
Skills
CAD
Solid Edge
ISO 13485
QMS
FMEA
Working at Freudenberg: We will wow your world!
Responsibilities:
•
Leads the design and development of complex medical devices from concept through to design freeze
•
Solves high-level engineering challenges using advanced materials knowledge, precision manufacturing methods, and data-driven decision making
•
Acts as a subject matter expert in catheter systems, extrusion-based assemblies, and biomaterials, influencing design direction and technical standards
•
Develops and executes verification and validation protocols (IQ/OQ/PQ), ensuring compliance with ISO 13485 and FDA 21 CFR Part 820
•
Manages cross-functional technical projects, balancing design intent, manufacturability, and regulatory requirements
•
Leads FMEA, risk analysis, and root cause investigations to ensure robust design and process outcomes
•
Provides technical mentoring and reviews for junior engineers and project teams, helping to build capability and ensure knowledge transfer
•
Drives innovation by exploring emerging technologies, novel components, and automation opportunities
•
Develops and maintains detailed documentation including DHFs, BOMs, drawings, and test reports in compliance with QMS requirements
•
Engages directly with customers to understand application needs, presenting technical solutions and leading design iterations
Qualifications:
•
Third-level qualification in Engineering or Science, preferably Mechanical or Biomedical; minimum Bachelor’s degree in Science, Technology, Engineering, or a related discipline (Mechanical, Manufacturing, Automation, or equivalent).
•
Proven design capability with CAD systems, ideally Solid Edge.
•
Senior-level candidates should have a minimum of 4 years’ relevant experience.
•
Excellent interpersonal and communication skills, with the ability to collaborate effectively across teams
Legal
The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.
VistaMed Ltd.
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