1,832 R D Engineer jobs in Ireland
Product Development Engineer
Dublin, Leinster
Pale Blue Dot® Recruitment
Posted 8 days ago
Job Viewed
Job Description
Product Development Engineer – Medical Device Industry
We are seeking a highly skilled and motivated Product Development Engineer to join a fast-paced and innovative medical device team. This role is central to the design, development, and optimization of next-generation medical technologies, involving both hardware and software components. You will work cross-functionally to bring products from concept through to commercialization, ensuring compliance with regulatory standards and a strong focus on patient outcomes.
Responsibilities Include but are not Limited to:
Lead product development activities from design and prototyping to testing, validation, and market launch.
Collaborate with Operations, QA/RA, Technical Support, and Commercial teams to ensure smooth and compliant product development.
Partner with Product Management to define product strategies and technical requirements aligned with business goals.
Define design inputs, conduct feasibility studies, and contribute to the development of technical documentation including design history files and technical files.
Work on embedded systems, firmware, and software development to support fully integrated device functionality.
Conduct risk assessments and support the implementation of risk management strategies.
Optimize designs for manufacturability, scalability, and performance.
Manage the full product development lifecycle and ensure adherence to regulatory and quality requirements.
Participate in design reviews and prototype evaluations, offering technical guidance across departments.
Troubleshoot and resolve product issues during both development and post-market stages.
Degree in Engineering (Biomedical, Mechanical, Electrical, or a related discipline).
Minimum of 5 years' experience in product development, preferably in the medical device sector or a closely related field.
Strong experience with embedded systems, firmware, and software development.
Proven background in taking medical devices from concept to market launch.
Solid understanding of design controls, validation, and regulatory compliance (e.g., FDA, ISO 13485).
Proficient in both hardware and software product design, prototyping, and testing.
Knowledge of mechanical engineering principles, manufacturing processes, and materials.
Familiar with risk management techniques (e.g., FMEA) and regulatory documentation practices.
Skilled in CAD tools (e.g., SolidWorks, AutoCAD), MATLAB, C/C++, Python, and embedded platforms.
Core Competencies:
Strong analytical, problem-solving, and decision-making skills.
Excellent communication skills, both verbal and written.
Proven ability to work cross-functionally with engineering, regulatory, quality, and commercial teams.
Highly detail-oriented, proactive, and adaptable with a continuous improvement mindset.
Preferred & Desirable Qualifications:
Experience with auditory or wearable medical technologies.
Familiarity with FDA 21 CFR Part 820, ISO 13485, ISO 14971 standards.
Experience with PLM systems and product lifecycle documentation.
Lean/Six Sigma or other continuous improvement methodologies.
Ability to mentor and train junior team members.
Track record of process and product optimization with risk mitigation.
Flexibility to work in a dynamic and evolving environment.
Willingness to travel internationally as required.
Note: By applying for this position, you may also be considered by Pale Blue Dot® Recruitment for other or future related vacancies.
Pale Blue Dot® Recruitment
The Experts in STEM Workforce Solutions
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0
Senior Product Development Engineer
Galway, Connacht
Life Science Recruitment Ltd
Posted today
Job Viewed
Job Description
Job Title: Senior Product Development Engineer Location: Parkmore, Galway Benefits: Excellent salary, bonus, healthcare and pension. Company: My client are a trusted provider of design and contract manufacturing solutions dedicated primarily to the medical device field. They support the full lifecycle of medical product developmentfrom innovation, industrial design, and engineering, to component manufacturing, assembly, packaging, and supply chain managementserving both multinational corporations and agile start-ups. Duties & Responsibilities include but are not limited to: Lead product development activity for customer projects (which may include multiple simultaneous projects) to ensure that customer requirements are defined, resolved into solutions and translated into product specifications for transfer to production. Engineering development of user focused product solutions that are optimised for manufacture. Lead (and for certain program support) the following product development activities: Concept development, Engineering, Design Verification stages of new product developments. Delivery of Mechanical Design solutions for early stage and end stage product development. Risk assessment, Risk Management as per ISO14971. Prototyping and testing concept designs and initial engineering builds. CAD development & tolerance stack up analysis - SolidWorks 3D CAD proficient in complex assemblies, surface modelling - 2d drawings. Pilot production trials to assess concept feasibility & troubleshoot design risk. Development of Product Specification & Test Method Development and documentation of such in Product Input/Output format. Statistical analysis of product test data using Minitab or equivalent software. Design verification, including development of test protocols & conducting of testing as per ISO13485 / customer requirements. Work with Design team to define & complete product validation and usability testing. Work with customers to complete Design & Technical reviews. Work with Process Development team and Production teams to complete transfer to production and pre-production planning. Work with the PM to define, plan, track and report on Product Development projects; this should include use of Work Breakdown Structures, Project Plans, Costing etc. (for smaller program the engineering lead may be the PM). Lead development of project proposals outlining cost, schedule, risk etc. & liaise with customers to present and review proposals to secure project sale. Work with Quality team to evaluate product non-conformances to assist in root cause analysis and recommend design modifications if appropriate. Education & Experience Required : Minimum 5 years experience in product development for medical devices, ideally in highly regulated Class III devices. Demonstrated understanding of various types of manufacturing, mechanisms, materials, tolerance-analysis and design-for-manufacturing is required. Mechanical Design experience required. Highly experienced in product specification design; translation of design inputs to engineering outputs, tolerance stack up analysis, as well as product testing; limit challenge testing, test method development, test method validation etc. Experience of working under medical device design controls, with proven knowledge of design verification/validation and design/process FMEAs is required. Experience of medical device regulations including GMP (Good Manufacturing Practices), QSR (Quality Systems Regulations) and ISO quality requirements is required. Experienced in Risk Management for medical devices and associated documentation processes. Excellent problem solving, decision making, and root cause analysis skills are required. Experience designing for manufacturability particularly for plastics, and experience with related supplier management. Highly experienced in project management, from conception to delivery; strong initiative and follow through in executing project responsibilities, overcoming obstacles and balancing multiple priorities effectively through strong technical and/or project leadership experience is required. Excellent communication skills, both written and verbal; the ability to effectively communicate concepts, ideas and knowledge to all levels of the organisation is required. Experience in team management and a demonstrated track-record of being part of successful cross-functional product development teams is required. Proficiency in 3D CAD (e.g. Solidworks) and MS Office Suite is required. Does this sound like your next career move? To apply and For more info forward your application to the link provided or contact me on OR Benefits: Healthcare + Annual Bonus + Pension
This advertiser has chosen not to accept applicants from your region.
1
Senior product development engineer
Galway, Connacht
Life Science Recruitment Ltd
Posted today
Job Viewed
Job Description
Job Title: Senior Product Development Engineer Location: Parkmore, Galway Benefits: Excellent salary, bonus, healthcare and pension.
Company: My client are a trusted provider of design and contract manufacturing solutions dedicated primarily to the medical device field.
They support the full lifecycle of medical product developmentfrom innovation, industrial design, and engineering, to component manufacturing, assembly, packaging, and supply chain managementserving both multinational corporations and agile start-ups.
Duties & Responsibilities include but are not limited to: Lead product development activity for customer projects (which may include multiple simultaneous projects) to ensure that customer requirements are defined, resolved into solutions and translated into product specifications for transfer to production.
Engineering development of user focused product solutions that are optimised for manufacture.
Lead (and for certain program support) the following product development activities: Concept development, Engineering, Design Verification stages of new product developments.
Delivery of Mechanical Design solutions for early stage and end stage product development.
Risk assessment, Risk Management as per ISO14971.
Prototyping and testing concept designs and initial engineering builds.
CAD development & tolerance stack up analysis - Solid Works 3 D CAD proficient in complex assemblies, surface modelling - 2d drawings.
Pilot production trials to assess concept feasibility & troubleshoot design risk.
Development of Product Specification & Test Method Development and documentation of such in Product Input/Output format.
Statistical analysis of product test data using Minitab or equivalent software.
Design verification, including development of test protocols & conducting of testing as per ISO13485 / customer requirements.
Work with Design team to define & complete product validation and usability testing.
Work with customers to complete Design & Technical reviews.
Work with Process Development team and Production teams to complete transfer to production and pre-production planning.
Work with the PM to define, plan, track and report on Product Development projects; this should include use of Work Breakdown Structures, Project Plans, Costing etc.
(for smaller program the engineering lead may be the PM).
Lead development of project proposals outlining cost, schedule, risk etc.
& liaise with customers to present and review proposals to secure project sale.
Work with Quality team to evaluate product non-conformances to assist in root cause analysis and recommend design modifications if appropriate.
Education & Experience Required : Minimum 5 years experience in product development for medical devices, ideally in highly regulated Class III devices.
Demonstrated understanding of various types of manufacturing, mechanisms, materials, tolerance-analysis and design-for-manufacturing is required.
Mechanical Design experience required.
Highly experienced in product specification design; translation of design inputs to engineering outputs, tolerance stack up analysis, as well as product testing; limit challenge testing, test method development, test method validation etc.
Experience of working under medical device design controls, with proven knowledge of design verification/validation and design/process FMEAs is required.
Experience of medical device regulations including GMP (Good Manufacturing Practices), QSR (Quality Systems Regulations) and ISO quality requirements is required.
Experienced in Risk Management for medical devices and associated documentation processes.
Excellent problem solving, decision making, and root cause analysis skills are required.
Experience designing for manufacturability particularly for plastics, and experience with related supplier management.
Highly experienced in project management, from conception to delivery; strong initiative and follow through in executing project responsibilities, overcoming obstacles and balancing multiple priorities effectively through strong technical and/or project leadership experience is required.
Excellent communication skills, both written and verbal; the ability to effectively communicate concepts, ideas and knowledge to all levels of the organisation is required.
Experience in team management and a demonstrated track-record of being part of successful cross-functional product development teams is required.
Proficiency in 3 D CAD (e.g.
Solidworks) and MS Office Suite is required.
Does this sound like your next career move? To apply and For more info forward your application to the link provided or contact me on OR Benefits: Healthcare + Annual Bonus + Pension
Company: My client are a trusted provider of design and contract manufacturing solutions dedicated primarily to the medical device field.
They support the full lifecycle of medical product developmentfrom innovation, industrial design, and engineering, to component manufacturing, assembly, packaging, and supply chain managementserving both multinational corporations and agile start-ups.
Duties & Responsibilities include but are not limited to: Lead product development activity for customer projects (which may include multiple simultaneous projects) to ensure that customer requirements are defined, resolved into solutions and translated into product specifications for transfer to production.
Engineering development of user focused product solutions that are optimised for manufacture.
Lead (and for certain program support) the following product development activities: Concept development, Engineering, Design Verification stages of new product developments.
Delivery of Mechanical Design solutions for early stage and end stage product development.
Risk assessment, Risk Management as per ISO14971.
Prototyping and testing concept designs and initial engineering builds.
CAD development & tolerance stack up analysis - Solid Works 3 D CAD proficient in complex assemblies, surface modelling - 2d drawings.
Pilot production trials to assess concept feasibility & troubleshoot design risk.
Development of Product Specification & Test Method Development and documentation of such in Product Input/Output format.
Statistical analysis of product test data using Minitab or equivalent software.
Design verification, including development of test protocols & conducting of testing as per ISO13485 / customer requirements.
Work with Design team to define & complete product validation and usability testing.
Work with customers to complete Design & Technical reviews.
Work with Process Development team and Production teams to complete transfer to production and pre-production planning.
Work with the PM to define, plan, track and report on Product Development projects; this should include use of Work Breakdown Structures, Project Plans, Costing etc.
(for smaller program the engineering lead may be the PM).
Lead development of project proposals outlining cost, schedule, risk etc.
& liaise with customers to present and review proposals to secure project sale.
Work with Quality team to evaluate product non-conformances to assist in root cause analysis and recommend design modifications if appropriate.
Education & Experience Required : Minimum 5 years experience in product development for medical devices, ideally in highly regulated Class III devices.
Demonstrated understanding of various types of manufacturing, mechanisms, materials, tolerance-analysis and design-for-manufacturing is required.
Mechanical Design experience required.
Highly experienced in product specification design; translation of design inputs to engineering outputs, tolerance stack up analysis, as well as product testing; limit challenge testing, test method development, test method validation etc.
Experience of working under medical device design controls, with proven knowledge of design verification/validation and design/process FMEAs is required.
Experience of medical device regulations including GMP (Good Manufacturing Practices), QSR (Quality Systems Regulations) and ISO quality requirements is required.
Experienced in Risk Management for medical devices and associated documentation processes.
Excellent problem solving, decision making, and root cause analysis skills are required.
Experience designing for manufacturability particularly for plastics, and experience with related supplier management.
Highly experienced in project management, from conception to delivery; strong initiative and follow through in executing project responsibilities, overcoming obstacles and balancing multiple priorities effectively through strong technical and/or project leadership experience is required.
Excellent communication skills, both written and verbal; the ability to effectively communicate concepts, ideas and knowledge to all levels of the organisation is required.
Experience in team management and a demonstrated track-record of being part of successful cross-functional product development teams is required.
Proficiency in 3 D CAD (e.g.
Solidworks) and MS Office Suite is required.
Does this sound like your next career move? To apply and For more info forward your application to the link provided or contact me on OR Benefits: Healthcare + Annual Bonus + Pension
This advertiser has chosen not to accept applicants from your region.
2
New Product Development Technologist (Food)
Monaghan, Ulster
Ascension
Posted today
Job Viewed
Job Description
Role Purpose The Product Technologist will play a key role in supporting the development and launch of new food products, ensuring they meet customer, regulatory, and quality requirements. This role bridges product development and technical compliance, ensuring smooth project delivery from concept to launch. Key Responsibilities Support the end-to-end NPD process, from initial concept through to factory trials and product launch. Manage product specifications, ensuring accuracy and compliance with customer, legal, and internal requirements. Liaise with suppliers to obtain raw material information, certifications, and technical data. Prepare customer documentation including product specifications, artwork approvals, and product information packs. Assist with factory trials, capturing process data and ensuring scale-up feasibility. Maintain accurate records of trials, formulations, and technical documentation. Support the Technical and Quality teams with product-related queries and customer audits. Ensure adherence to food safety, HACCP, and allergen control requirements. Skills: npd food technologist new product development Benefits: Excellent
This advertiser has chosen not to accept applicants from your region.
3
New product development technologist (food)
Monaghan, Ulster
Ascension Executive
Posted today
Job Viewed
Job Description
Role Purpose The Product Technologist will play a key role in supporting the development and launch of new food products, ensuring they meet customer, regulatory, and quality requirements.
This role bridges product development and technical compliance, ensuring smooth project delivery from concept to launch.
Key Responsibilities Support the end-to-end NPD process, from initial concept through to factory trials and product launch.
Manage product specifications, ensuring accuracy and compliance with customer, legal, and internal requirements.
Liaise with suppliers to obtain raw material information, certifications, and technical data.
Prepare customer documentation including product specifications, artwork approvals, and product information packs.
Assist with factory trials, capturing process data and ensuring scale-up feasibility.
Maintain accurate records of trials, formulations, and technical documentation.
Support the Technical and Quality teams with product-related queries and customer audits.
Ensure adherence to food safety, HACCP, and allergen control requirements.
Skills: npd food technologist new product development Benefits: Excellent
This role bridges product development and technical compliance, ensuring smooth project delivery from concept to launch.
Key Responsibilities Support the end-to-end NPD process, from initial concept through to factory trials and product launch.
Manage product specifications, ensuring accuracy and compliance with customer, legal, and internal requirements.
Liaise with suppliers to obtain raw material information, certifications, and technical data.
Prepare customer documentation including product specifications, artwork approvals, and product information packs.
Assist with factory trials, capturing process data and ensuring scale-up feasibility.
Maintain accurate records of trials, formulations, and technical documentation.
Support the Technical and Quality teams with product-related queries and customer audits.
Ensure adherence to food safety, HACCP, and allergen control requirements.
Skills: npd food technologist new product development Benefits: Excellent
This advertiser has chosen not to accept applicants from your region.
4
Associate Director, Pen Injector Product Development
Dún Laoghaire, Leinster
embecta
Posted today
Job Viewed
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.
embecta, formerly part of BD, is one of the largest pure-play diabetes care companies in the world, leveraging its nearly 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.
This role leads the development of core technologies within R&D, guiding strategic direction across innovation projects. You'll evaluate emerging trends, advise on future technology choices, and help build lasting technical expertise to drive product advancement.
**Responsibilities**
+ Partner with key stakeholders across the various functions, to align objectives by understanding market opportunities, strategic goals and roadmaps
+ Develop, implement, and coordinate strategies as they relate to Pen Injectors and Auto Injectors
+ Understand the current market landscape of pen injectors and auto injectors, their strengths and weaknesses and associated opportunities for embecta.
+ Ensure that all new products are Designed For high volume Manufacturing and Assembly (DFMA)
+ Followsdesign, quality,and safetyguidelinesbasedonGMP, FDA, andISOguidelinesand relatedembecta Quality and Safety Standards and Practices
+ Leads and motivates a lean, high performing team in the development of new products that increase revenue for embecta with a short payback period and quick launch windows.
+ Leverage the Engineering Group in Dún Laoghaire, Ireland in alignment with the Director of the Engineering Group.
+ Bring an exciting energy to the Dún Laoghaire team, identifying high potential candidates for development and possible rotation through the Pen Injector Development Team.
**Education and Experience**
+ Bachelor's degree in Mechanical Engineering or related technical field is required; advanced degree is a plus
+ Minimum of 15 years relevant experience in successful cross-functional matrix organizations
+ 10+ years of experience in medical industries developing mechanical-based consumable Medical Devices
+ Experience working with and managing internal talent, as well as third-party consultants and service providers
+ Excellent presentation and communication skills, including executive presentation
+ Superior analytical, evaluative, and problem-solving abilities
#LI-HYBRID
#LI-DF1
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.
**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.
embecta, formerly part of BD, is one of the largest pure-play diabetes care companies in the world, leveraging its nearly 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.
This role leads the development of core technologies within R&D, guiding strategic direction across innovation projects. You'll evaluate emerging trends, advise on future technology choices, and help build lasting technical expertise to drive product advancement.
**Responsibilities**
+ Partner with key stakeholders across the various functions, to align objectives by understanding market opportunities, strategic goals and roadmaps
+ Develop, implement, and coordinate strategies as they relate to Pen Injectors and Auto Injectors
+ Understand the current market landscape of pen injectors and auto injectors, their strengths and weaknesses and associated opportunities for embecta.
+ Ensure that all new products are Designed For high volume Manufacturing and Assembly (DFMA)
+ Followsdesign, quality,and safetyguidelinesbasedonGMP, FDA, andISOguidelinesand relatedembecta Quality and Safety Standards and Practices
+ Leads and motivates a lean, high performing team in the development of new products that increase revenue for embecta with a short payback period and quick launch windows.
+ Leverage the Engineering Group in Dún Laoghaire, Ireland in alignment with the Director of the Engineering Group.
+ Bring an exciting energy to the Dún Laoghaire team, identifying high potential candidates for development and possible rotation through the Pen Injector Development Team.
**Education and Experience**
+ Bachelor's degree in Mechanical Engineering or related technical field is required; advanced degree is a plus
+ Minimum of 15 years relevant experience in successful cross-functional matrix organizations
+ 10+ years of experience in medical industries developing mechanical-based consumable Medical Devices
+ Experience working with and managing internal talent, as well as third-party consultants and service providers
+ Excellent presentation and communication skills, including executive presentation
+ Superior analytical, evaluative, and problem-solving abilities
#LI-HYBRID
#LI-DF1
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.
This advertiser has chosen not to accept applicants from your region.
5
Associate Director, Pen Injector Product Development
Dublin, Leinster
Embecta
Posted today
Job Viewed
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. 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. embecta, formerly part of BD, is one of the largest pure-play diabetes care companies in the world, leveraging its nearly 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. This role leads the development of core technologies within R&D, guiding strategic direction across innovation projects. You'll evaluate emerging trends, advise on future technology choices, and help build lasting technical expertise to drive product advancement. Responsibilities Partner with key stakeholders across the various functions, to align objectives by understanding market opportunities, strategic goals and roadmaps Develop, implement, and coordinate strategies as they relate to Pen Injectors and Auto Injectors Understand the current market landscape of pen injectors and auto injectors, their strengths and weaknesses and associated opportunities for embecta. Ensure that all new products are Designed For high volume Manufacturing and Assembly (DFMA) Follows design, quality, and safety guidelines based on GMP, FDA, and ISO guidelines and related embecta Quality and Safety Standards and Practices Leads and motivates a lean, high performing team in the development of new products that increase revenue for embecta with a short payback period and quick launch windows. Leverage the Engineering Group in Dn Laoghaire, Ireland in alignment with the Director of the Engineering Group. Bring an exciting energy to the Dn Laoghaire team, identifying high potential candidates for development and possible rotation through the Pen Injector Development Team. Education and Experience Bachelor's degree in Mechanical Engineering or related technical field is required; advanced degree is a plus Minimum of 15 years relevant experience in successful cross-functional matrix organizations 10+ years of experience in medical industries developing mechanical-based consumable Medical Devices Experience working with and managing internal talent, as well as third-party consultants and service providers Excellent presentation and communication skills, including executive presentation Superior analytical, evaluative, and problem-solving abilities #LI-HYBRID #LI-DF1 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.
This advertiser has chosen not to accept applicants from your region.
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6
Associate Director Pen Injector Product Development
Dublin, Leinster
Collins McNicholas
Posted today
Job Viewed
Job Description
Our client a global medical device company have a new leadership opportunity. We are looking for a seasoned Pen Injector Product Developer to join a leading global medical device company in South Dublin as an Associate Director. This is a senior leadership role within R&D, focused on guiding the development of core technologies for Pen Injectors and Auto Injectors. You will shape strategic directions across innovation projects, evaluate emerging trends, and help build lasting technical expertise to advance product development. Key Responsibilities of the Associate Director: Partner with stakeholders across multiple functions to align objectives, leveraging market insights, strategic goals, and product roadmaps. Develop, implement, and coordinate strategies related to Pen and Auto Injectors. Analyze the competitive landscape, identifying strengths, weaknesses, and opportunities in injector technologies. Ensure new products are designed for high-volume manufacturing and assembly (DFMA). Uphold design, quality, and safety standards in line with GMP, FDA, ISO, and internal quality practices. Lead and inspire a lean, high-performing team to deliver innovative products with short payback periods and rapid launch timelines. Collaborate closely with the Engineering Group in Dn Laoghaire to maximize talent development and technical impact. Mentor high-potential team members and identify opportunities for growth within the Pen Injector Development team. Qualifications & Experience Pen Injector Design Experience is highly desirable. Degree in Mechanical Engineering or a related technical field; advanced degree preferred. Minimum of 15 years of relevant experience in successful cross-functional matrix organizations. At least 10 years experience in the medical device industry, particularly developing mechanical-based consumable devices. Proven experience managing internal teams as well as third-party consultants and service providers. Exceptional presentation and communication skills, including executive-level presentations. Strong analytical, evaluative, and problem-solving capabilities. Why This Role is Exciting Lead breakthrough innovation in diabetes care devices impacting millions of lives globally. Work in a dynamic, inclusive environment that encourages curiosity, growth, and creativity. Shape the next generation of medical devices with high visibility and meaningful impact. For a confidential discussion about the role of Associate Director in South Dublin, please reach out to me directly Skills: associate director pen injector product developer pen injector
This advertiser has chosen not to accept applicants from your region.
7
Associate director, pen injector product development
Dublin, Leinster
Embecta
Posted today
Job Viewed
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.
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.
embecta, formerly part of BD, is one of the largest pure-play diabetes care companies in the world, leveraging its nearly 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.
This role leads the development of core technologies within R&D, guiding strategic direction across innovation projects.
You'll evaluate emerging trends, advise on future technology choices, and help build lasting technical expertise to drive product advancement.
Responsibilities Partner with key stakeholders across the various functions, to align objectives by understanding market opportunities, strategic goals and roadmaps Develop, implement, and coordinate strategies as they relate to Pen Injectors and Auto Injectors Understand the current market landscape of pen injectors and auto injectors, their strengths and weaknesses and associated opportunities for embecta.
Ensure that all new products are Designed For high volume Manufacturing and Assembly (DFMA) Follows design, quality, and safety guidelines based on GMP, FDA, and ISO guidelines and related embecta Quality and Safety Standards and Practices Leads and motivates a lean, high performing team in the development of new products that increase revenue for embecta with a short payback period and quick launch windows.
Leverage the Engineering Group in Dn Laoghaire, Ireland in alignment with the Director of the Engineering Group.
Bring an exciting energy to the Dn Laoghaire team, identifying high potential candidates for development and possible rotation through the Pen Injector Development Team.
Education and Experience Bachelor's degree in Mechanical Engineering or related technical field is required; advanced degree is a plus Minimum of 15 years relevant experience in successful cross-functional matrix organizations 10+ years of experience in medical industries developing mechanical-based consumable Medical Devices Experience working with and managing internal talent, as well as third-party consultants and service providers Excellent presentation and communication skills, including executive presentation Superior analytical, evaluative, and problem-solving abilities #LI-HYBRID #LI-DF1 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.
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.
embecta, formerly part of BD, is one of the largest pure-play diabetes care companies in the world, leveraging its nearly 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.
This role leads the development of core technologies within R&D, guiding strategic direction across innovation projects.
You'll evaluate emerging trends, advise on future technology choices, and help build lasting technical expertise to drive product advancement.
Responsibilities Partner with key stakeholders across the various functions, to align objectives by understanding market opportunities, strategic goals and roadmaps Develop, implement, and coordinate strategies as they relate to Pen Injectors and Auto Injectors Understand the current market landscape of pen injectors and auto injectors, their strengths and weaknesses and associated opportunities for embecta.
Ensure that all new products are Designed For high volume Manufacturing and Assembly (DFMA) Follows design, quality, and safety guidelines based on GMP, FDA, and ISO guidelines and related embecta Quality and Safety Standards and Practices Leads and motivates a lean, high performing team in the development of new products that increase revenue for embecta with a short payback period and quick launch windows.
Leverage the Engineering Group in Dn Laoghaire, Ireland in alignment with the Director of the Engineering Group.
Bring an exciting energy to the Dn Laoghaire team, identifying high potential candidates for development and possible rotation through the Pen Injector Development Team.
Education and Experience Bachelor's degree in Mechanical Engineering or related technical field is required; advanced degree is a plus Minimum of 15 years relevant experience in successful cross-functional matrix organizations 10+ years of experience in medical industries developing mechanical-based consumable Medical Devices Experience working with and managing internal talent, as well as third-party consultants and service providers Excellent presentation and communication skills, including executive presentation Superior analytical, evaluative, and problem-solving abilities #LI-HYBRID #LI-DF1 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.
This advertiser has chosen not to accept applicants from your region.
8
Senior Research & Development Engineer I Sustaining & Lifecycle
Galway, Connacht
J&J Family of Companies
Posted today
Job Viewed
Job Description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Function:**
R&D Product Development
**Job Sub** **Function:**
Biomedical Engineering
**Job Category:**
Scientific/Technology
**All Job Posting Locations:**
Galway, Ireland
**Job Description:**
**Role: Senior Research & Development Engineer I Sustaining & Lifecycle Management**
**Location:** Ballybrit, Galway
**Reports to:** R&D Project Manager
**Live Our Credo & Pursue Our Purpose:**
As part of the Johnson & Johnson family of companies, Our Purpose is 'We blend heart, science and ingenuity to profoundly change the trajectory of health for humanity.' We are guided by the values in Our Credo. With responsibility to patients, employees, communities, and stakeholders, Our Credo puts the needs of each of those first.
**Diversity, Equity & Inclusion:**
For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.
We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences.
That is why we in Ireland are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means "You Belong".
**JOHNSON AND JOHNSON MEDTECH, NEUROVASCULAR:**
JOHNSON AND JOHNSON MEDTECH, NEUROVASCULAR, part of Johnson & Johnson Medical Devices Companies, is a global leader in neurovascular care. Our commitment to changing the trajectory of stroke is inspired by our long heritage and dedication to helping physicians protect people from a lifetime of hardship. JOHNSON AND JOHNSON MEDTECH, NEUROVASCULAR offers a broad portfolio of devices used in the endovascular treatment of haemorrhagic and ischemic stroke.
**What is it like to work at JOHNSON AND JOHNSON MEDTECH, NEUROVASCULAR Galway?**
+ Culturally, we are putting the needs of Our Credo stakeholders first through pursuing the highest standards of quality, compliance, and ethics, ensuring everyday actions contribute to Our Purpose.
+ We are continuing to better our understanding of clot science through our Neuro Thromboembolic Initiative (NTI). This is a commitment to advance the treatment of stroke through interdisciplinary collaboration and investment in clot and stroke research. How we understand clots and their behaviour enhances our opportunity to design devices that improve patient outcomes and advance the treatment of acute ischemic stroke.
+ Strong new product pipeline and a fast-growing medical device company within J&J.
+ From a People perspective, we invest in our people, and take great pride in providing a positive work environment which respects diversity, supports wellbeing, and embraces innovation. This is empowered through our employee resource groups (ERGs) focused on further balances of gender, nationality, capability and more, including the additional attracting of qualified diverse candidates for our open roles.
**Job Summary:**
JOHNSON AND JOHNSON MEDTECH, NEUROVASCULAR a Johnson & Johnson company is recruiting for a Senior Research and Development Engineer, Sustaining and Lifecycle Management, in Galway Ireland.
The role of Senior R&D Engineer I supports managing and delivering R&D activities associated with the lifecycle management of the portfolio of products for treatment of acute ischemic stroke with significant technical challenges. Overall responsibility for various aspects of the product's lifecycle including material changes, process improvement, regulatory submissions, shelf-life studies, responding to sales & marketing requests, and returned product investigations.
**The responsibilities and the impact YOU will have:**
+ Acquire an in-depth knowledge of current products from a technical point of view: design, materials, performances, manufacturing process.
+ Product/Process optimization projects - in liaison with Supply Chain and Quality.
+ Support second supplier and/or technical transfer projects.
+ Manage project sub-parts, as part of a larger project team.
+ Provide direction to other team members, including mentoring and oversight of less experienced engineers or technicians.
+ Support regulatory submissions and lead additional Design Verification/Validation studies as required by regional authorities.
+ Lead product Shelf-Life studies through Design Verification testing.
+ Investigations on product complaints and analysis of returned devices
+ Support to CAPA and Non-Conformance process.
+ Evaluation and scoping of process changes, material changes, vendor changes.
+ Support to Labelling changes and implementation.
+ Support to Sales and Marketing for product characterization, competitive testing, field training.
+ Develop and deliver project plans to performance, time and cost targets.
+ Leverage and liaise with external resources, including suppliers, to achieve project goals.
+ Identify and manage of key risks throughout the product lifecycle.
+ Write procedures, protocols, specifications, and reports.
+ Evaluate and assess physician (user) techniques and develop product training materials.
+ Support developing marketing materials (presentations/videos/demos).
+ Other duties as assigned or required.
**We would love to hear from YOU, if you have the following essential requirements:**
+ A minimum of 4 years' experience in all stages of medical device design and development (including design with SolidWorks, prototyping, and testing) is required.
+ Specific experience on Medical Devices, cardiovascular or neurovascular implants or instruments including catheters, stents, delivery systems.
+ Strong design and technical ability based on a broad and deep knowledge of fundamental engineering principles.
+ Data review and statistical methods skills (Minitab).
+ Strong work ethic, creative problem solving, capable of working on own initiative.
+ Excellent writing, presentation, and verbal communication skills essential.
+ Results and deadline driven with an ability to handle multiple tasks and operate in a fast-paced environment.
+ Excellent interpersonal skills and ability to work with people to achieve results.
+ Highly motivated and an enthusiastic self-starter with the ability to work under own initiative and as a team player.
**Location & Travel**
+ This role will be an onsite role based in Galway, Ireland with flexible work arrangements from time to time in agreement with management and per the J&J Flexible Work policy.
+ As part of a global company, travel may be required from time to time, up to 20%.
**This is what awaits YOU:**
This is an opportunity to work with a ground-breaking biomedical. We are passionate about our work; we play vital roles across a range of professional disciplines, and care deeply about our customers and communities. At Johnson & Johnson, our culture enables dynamic and impactful careers.
Whether you're one of the people who already work here, or you're considering joining the team, we offer:
+ An opportunity to be part of a global market leader.
+ A dynamic and inspiring working environment.
+ Opportunities to work on challenging projects and assignments.
+ Possibilities for further personal and professional development/education.
**Equal Opportunity:**
All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
R&D Product Development
**Job Sub** **Function:**
Biomedical Engineering
**Job Category:**
Scientific/Technology
**All Job Posting Locations:**
Galway, Ireland
**Job Description:**
**Role: Senior Research & Development Engineer I Sustaining & Lifecycle Management**
**Location:** Ballybrit, Galway
**Reports to:** R&D Project Manager
**Live Our Credo & Pursue Our Purpose:**
As part of the Johnson & Johnson family of companies, Our Purpose is 'We blend heart, science and ingenuity to profoundly change the trajectory of health for humanity.' We are guided by the values in Our Credo. With responsibility to patients, employees, communities, and stakeholders, Our Credo puts the needs of each of those first.
**Diversity, Equity & Inclusion:**
For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.
We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences.
That is why we in Ireland are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means "You Belong".
**JOHNSON AND JOHNSON MEDTECH, NEUROVASCULAR:**
JOHNSON AND JOHNSON MEDTECH, NEUROVASCULAR, part of Johnson & Johnson Medical Devices Companies, is a global leader in neurovascular care. Our commitment to changing the trajectory of stroke is inspired by our long heritage and dedication to helping physicians protect people from a lifetime of hardship. JOHNSON AND JOHNSON MEDTECH, NEUROVASCULAR offers a broad portfolio of devices used in the endovascular treatment of haemorrhagic and ischemic stroke.
**What is it like to work at JOHNSON AND JOHNSON MEDTECH, NEUROVASCULAR Galway?**
+ Culturally, we are putting the needs of Our Credo stakeholders first through pursuing the highest standards of quality, compliance, and ethics, ensuring everyday actions contribute to Our Purpose.
+ We are continuing to better our understanding of clot science through our Neuro Thromboembolic Initiative (NTI). This is a commitment to advance the treatment of stroke through interdisciplinary collaboration and investment in clot and stroke research. How we understand clots and their behaviour enhances our opportunity to design devices that improve patient outcomes and advance the treatment of acute ischemic stroke.
+ Strong new product pipeline and a fast-growing medical device company within J&J.
+ From a People perspective, we invest in our people, and take great pride in providing a positive work environment which respects diversity, supports wellbeing, and embraces innovation. This is empowered through our employee resource groups (ERGs) focused on further balances of gender, nationality, capability and more, including the additional attracting of qualified diverse candidates for our open roles.
**Job Summary:**
JOHNSON AND JOHNSON MEDTECH, NEUROVASCULAR a Johnson & Johnson company is recruiting for a Senior Research and Development Engineer, Sustaining and Lifecycle Management, in Galway Ireland.
The role of Senior R&D Engineer I supports managing and delivering R&D activities associated with the lifecycle management of the portfolio of products for treatment of acute ischemic stroke with significant technical challenges. Overall responsibility for various aspects of the product's lifecycle including material changes, process improvement, regulatory submissions, shelf-life studies, responding to sales & marketing requests, and returned product investigations.
**The responsibilities and the impact YOU will have:**
+ Acquire an in-depth knowledge of current products from a technical point of view: design, materials, performances, manufacturing process.
+ Product/Process optimization projects - in liaison with Supply Chain and Quality.
+ Support second supplier and/or technical transfer projects.
+ Manage project sub-parts, as part of a larger project team.
+ Provide direction to other team members, including mentoring and oversight of less experienced engineers or technicians.
+ Support regulatory submissions and lead additional Design Verification/Validation studies as required by regional authorities.
+ Lead product Shelf-Life studies through Design Verification testing.
+ Investigations on product complaints and analysis of returned devices
+ Support to CAPA and Non-Conformance process.
+ Evaluation and scoping of process changes, material changes, vendor changes.
+ Support to Labelling changes and implementation.
+ Support to Sales and Marketing for product characterization, competitive testing, field training.
+ Develop and deliver project plans to performance, time and cost targets.
+ Leverage and liaise with external resources, including suppliers, to achieve project goals.
+ Identify and manage of key risks throughout the product lifecycle.
+ Write procedures, protocols, specifications, and reports.
+ Evaluate and assess physician (user) techniques and develop product training materials.
+ Support developing marketing materials (presentations/videos/demos).
+ Other duties as assigned or required.
**We would love to hear from YOU, if you have the following essential requirements:**
+ A minimum of 4 years' experience in all stages of medical device design and development (including design with SolidWorks, prototyping, and testing) is required.
+ Specific experience on Medical Devices, cardiovascular or neurovascular implants or instruments including catheters, stents, delivery systems.
+ Strong design and technical ability based on a broad and deep knowledge of fundamental engineering principles.
+ Data review and statistical methods skills (Minitab).
+ Strong work ethic, creative problem solving, capable of working on own initiative.
+ Excellent writing, presentation, and verbal communication skills essential.
+ Results and deadline driven with an ability to handle multiple tasks and operate in a fast-paced environment.
+ Excellent interpersonal skills and ability to work with people to achieve results.
+ Highly motivated and an enthusiastic self-starter with the ability to work under own initiative and as a team player.
**Location & Travel**
+ This role will be an onsite role based in Galway, Ireland with flexible work arrangements from time to time in agreement with management and per the J&J Flexible Work policy.
+ As part of a global company, travel may be required from time to time, up to 20%.
**This is what awaits YOU:**
This is an opportunity to work with a ground-breaking biomedical. We are passionate about our work; we play vital roles across a range of professional disciplines, and care deeply about our customers and communities. At Johnson & Johnson, our culture enables dynamic and impactful careers.
Whether you're one of the people who already work here, or you're considering joining the team, we offer:
+ An opportunity to be part of a global market leader.
+ A dynamic and inspiring working environment.
+ Opportunities to work on challenging projects and assignments.
+ Possibilities for further personal and professional development/education.
**Equal Opportunity:**
All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
This advertiser has chosen not to accept applicants from your region.
9