63 Ild Product Manager jobs in Ireland

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

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

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

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

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.

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.

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

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.

Optum is a global organisation that delivers care, aided by technology to help millions of people live healthier lives. The work you do with our team will directly improve health outcomes by connecting people with the care, pharmacy benefits, data and resources they need to feel their best. Here, you will find a culture guided by diversity and inclusion, talented peers, comprehensive benefits and career development opportunities. Come make an impact on the communities we serve as you help us advance health equity on a global scale. Join us to start **Caring. Connecting. Growing together.**
In healthcare, evolution doesn't just happen. It takes innovation, imagination, and a passion for solving problems in new and better ways. And innovation is taking place at a lightning-fast pace every day at Optum. 
As the fastest growing part of the UnitedHealth Group family of businesses, we're expanding our team in Ireland and creating excellent opportunities for those who want greater purpose and more impact in their work. We'll provide the investment, support, and resources to advance your career. You'll provide the talent, ambition, and drive.
Optum Rx is looking for an experienced, curious, and self-motivated individual to lead a team that will be responsible for the development of new products and services for the organization. Partnering with business stakeholders, data science teams and technology teams, you will build strong relationships with our internal stakeholders, acquiring knowledge of the business and driving strategic platform build. 
You will join a team of product managers, product owners, data scientists, and analysts who are responsible for building the pricing platform for over $100 Billion of prescription drug spend in the US Market annually. The team bring integrity, experience and calmness to what is a mammoth business. We have thousands of US clients, each with thousands of FDA approved drug prices to be managed.  We are using our predictive models to optimize millions of individual drug prices to ensure we deliver value for clients and ultimately people who are filling over 150 million prescriptions per year.
We are accountable to manage one of the most complex areas of UnitedHealth Group, one of the largest companies in the world. We have to bring initiative, innovative thinking and curiosity to constantly evolve in a highly regulated environment. The changes we make have impact the next day for millions of people in the US market. 
Our team culture is built on trust. We give our team the space they need to deliver results and the environment to ensure they can have fun doing it.
**Primary Responsibilities:  **
+ Roadmap ownership and prioritization 
+ Writing clear product requirements (PRDs, user stories) 
+ Stakeholder communication and alignment 
+ Familiarity with AI/ML concepts (model accuracy, training data, inference)
+ Own the product lifecycle from discovery to delivery 
+ Collaborate with the Lead Data Scientist to ensure AI features are feasible, ethical, and valuable 
+ Work closely with Product Owners to manage backlogs and sprint planning 
+ Represent the voice of the users in all product decisions 
+ Agile mindset product development
_You will be rewarded and recognised for your performance in an environment that will challenge you and give you clear direction on what it takes to succeed in your role, as well as providing development for other roles you may be interested in._
**Required Qualifications:**
+ Bachelor's degree (or higher) in a relevant subject or equivalent experience.
+ Proven extensive experience in product management 
+ Scaling Agile for Enterprise frameworks certifications ( SA, SP,  POPM)
+ Proven track record of managing all aspects of a successful product throughout its lifecycle 
+ Proven stakeholder management skills across multiple levels 
**Please note you must currently be eligible to work and remain indefinitely without any restrictions in the country to which you are making an application. Proof will be required to support your application.**
_All telecommuters will be required to adhere to the UnitedHealth Group's Telecommuter Policy._
_At UnitedHealth Group, our mission is to help people live healthier lives and make the health system work better for everyone. We believe everyone-of every race, gender, sexuality, age, location and income-deserves the opportunity to live their healthiest life. Today, however, there are still far too many barriers to good health which are disproportionately experienced by people of color, historically marginalised groups and those with lower incomes. We are committed to mitigating our impact on the environment and enabling and delivering equitable care that addresses health disparities and improves health outcomes - an enterprise priority reflected in our mission._
_Diversity creates a healthier atmosphere: Optum is an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to gender, civil status, family status, sexual orientation, disability, religion, age, race, and membership of the Traveller community, or any other characteristic protected by law. Optum is a drug-free workplace. © 2024 Optum Services (Ireland) Limited. All rights reserved._
#RPO #BBMEMEA