64 Research And Development Engineer jobs in Ireland
Senior Research & Development Engineer I Sustaining & Lifecycle
Galway, Connacht
J&J Family of Companies
Posted 3 days ago
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.
0
Principal Research & Development Engineer - Interventional Vascular Technologies
Galway, Connacht
J&J Family of Companies
Posted 3 days ago
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:**
R&D Mechanical Engineering
**Job Category:**
Scientific/Technology
**All Job Posting Locations:**
Galway, Ireland
**Job Description:**
**Role: Principal Research & Development Engineer - Interventional Vascular Technologies**
**Location:** Ballybrit, Galway
**Reports to:** Director of R&D or Senior R&D 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.
**About Johnson & Johnson MedTech**
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at is it like to work at Johnson & Johnson Medtech | Neurovascular**
+ 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, overall, advance the treatment of acute ischemic stroke.
+ Strong new product pipeline and one of fastest growing areas 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 & Johnson Medtech | Neurovascular is recruiting for a **Principal R&D Engineer** in Galway, Ireland.
The Principal R&D Engineer will be responsible for providing technical leadership in the design and development of vascular interventional devices from early stage to commercialization. Overall responsibility for technical aspects of new product development projects, including product specification generation and identification of optimal solution through design development, technical risk management and test capability development.
**The responsibilities and the impact YOU will have:**
**Technical Leadership, Product & Process Development:**
+ Cross project ownership of device design and development, working with design engineers to identify novel solutions to meet product performance requirements while leveraging existing capabilities to meet cost of goods targets.
+ Provide technical leadership and take ownership of critical technical tasks in the execution of product development projects.
+ Design new products, optimise product performance and refine product design to meet technical specifications and unit cost target.
+ Leading and developing project engineers, identifying and implementing best practice in the design and development of catheters
+ Identify and manage technical risk across projects, in partnership with project leads.
+ Build and test prototypes, analyse test data and interpret to identify optimal solution(s).
+ Develop test capability to evaluate product performance and safety requirements.
+ Identify and support development of processes for new products.
**Culture -Improving the Way We Work & Building Capability**
+ Foster a culture of creativity; generate creative product solutions to address unmet needs.
+ Mentor those around you to grow in capability by open questioning to drive self-reflection and development.
+ Actively identify technical and adaptive opportunities for improvements and take action to address.
**Customer Connection to Drive Innovation:**
+ Liaise with key opinion leaders to develop a deep understanding of the disease state, gather user needs; and articulate throughout the team.
+ Attend external meetings with key opinion leaders to present the product portfolio and gain feedback on new product development.
+ Support generation of Intellectual Property by filing new ideas and drafting patents as required.
**We would love to hear from YOU, if you have the following essential requirements:**
**Qualifications -**
+ Honours degree in Mechanical or Biomedical Engineering or equivalent.
+ Extensive experience in the medical device industry.
**Experience and skills -**
+ Strong technical leadership capability in the development of new products, expert understanding of disease state and generates creative product solutions to address unmet needs.
+ Specific experience in cardiovascular, peripheral or neurovascular implants an advantage.
+ Excellent technical problem solving and analytical ability.
+ Strong device design, development and technical ability is essential, based on a solid foundation of fundamental engineering principles.
+ Data review and statistical methods expertise.
+ Experience of intellectual property generation and filing.
+ Ability to communicate clearly, accurately, and directly, both verbally and in writing, to a widely varied audience.
+ Creative problem solver.
+ 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 will be required from time to time, up to 20%
**This is what awaits YOU at J&J:**
This is an opportunity to work with a ground-breaking biomedical operation and to be a member of a Johnson & Johnson company, with an excellent record in employee continuous professional development and business improvement.
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.
+ Excellent benefits.
**Equal Opportunity:**
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. 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:**
R&D Mechanical Engineering
**Job Category:**
Scientific/Technology
**All Job Posting Locations:**
Galway, Ireland
**Job Description:**
**Role: Principal Research & Development Engineer - Interventional Vascular Technologies**
**Location:** Ballybrit, Galway
**Reports to:** Director of R&D or Senior R&D 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.
**About Johnson & Johnson MedTech**
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at is it like to work at Johnson & Johnson Medtech | Neurovascular**
+ 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, overall, advance the treatment of acute ischemic stroke.
+ Strong new product pipeline and one of fastest growing areas 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 & Johnson Medtech | Neurovascular is recruiting for a **Principal R&D Engineer** in Galway, Ireland.
The Principal R&D Engineer will be responsible for providing technical leadership in the design and development of vascular interventional devices from early stage to commercialization. Overall responsibility for technical aspects of new product development projects, including product specification generation and identification of optimal solution through design development, technical risk management and test capability development.
**The responsibilities and the impact YOU will have:**
**Technical Leadership, Product & Process Development:**
+ Cross project ownership of device design and development, working with design engineers to identify novel solutions to meet product performance requirements while leveraging existing capabilities to meet cost of goods targets.
+ Provide technical leadership and take ownership of critical technical tasks in the execution of product development projects.
+ Design new products, optimise product performance and refine product design to meet technical specifications and unit cost target.
+ Leading and developing project engineers, identifying and implementing best practice in the design and development of catheters
+ Identify and manage technical risk across projects, in partnership with project leads.
+ Build and test prototypes, analyse test data and interpret to identify optimal solution(s).
+ Develop test capability to evaluate product performance and safety requirements.
+ Identify and support development of processes for new products.
**Culture -Improving the Way We Work & Building Capability**
+ Foster a culture of creativity; generate creative product solutions to address unmet needs.
+ Mentor those around you to grow in capability by open questioning to drive self-reflection and development.
+ Actively identify technical and adaptive opportunities for improvements and take action to address.
**Customer Connection to Drive Innovation:**
+ Liaise with key opinion leaders to develop a deep understanding of the disease state, gather user needs; and articulate throughout the team.
+ Attend external meetings with key opinion leaders to present the product portfolio and gain feedback on new product development.
+ Support generation of Intellectual Property by filing new ideas and drafting patents as required.
**We would love to hear from YOU, if you have the following essential requirements:**
**Qualifications -**
+ Honours degree in Mechanical or Biomedical Engineering or equivalent.
+ Extensive experience in the medical device industry.
**Experience and skills -**
+ Strong technical leadership capability in the development of new products, expert understanding of disease state and generates creative product solutions to address unmet needs.
+ Specific experience in cardiovascular, peripheral or neurovascular implants an advantage.
+ Excellent technical problem solving and analytical ability.
+ Strong device design, development and technical ability is essential, based on a solid foundation of fundamental engineering principles.
+ Data review and statistical methods expertise.
+ Experience of intellectual property generation and filing.
+ Ability to communicate clearly, accurately, and directly, both verbally and in writing, to a widely varied audience.
+ Creative problem solver.
+ 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 will be required from time to time, up to 20%
**This is what awaits YOU at J&J:**
This is an opportunity to work with a ground-breaking biomedical operation and to be a member of a Johnson & Johnson company, with an excellent record in employee continuous professional development and business improvement.
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.
+ Excellent benefits.
**Equal Opportunity:**
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. 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.
1
Principal Research and Development Engineer
Galway, Connacht
€125000 - €150000 Annually
Life Science Recruitment
Posted 6 days ago
Job Viewed
Job Description
Overview
Job title: Principal Research & Development Engineer - Interventional Vascular Technologies
Location: Ballybrit, Galway
Benefits: Top salary, bonus, pension and healthcare
Company:
My client are experts in the Medical Device Technology fueled by innovation at the intersection of biology and technology. Continuing to better their understanding of clot science, through our Neuro Thromboembolic Initiative (NTI). Strong new product pipeline and takes great pride in providing a positive work environment which respects diversity, supports wellbeing, and embraces innovation.
As a Principal R&D Engineer you will be responsible for providing technical leadership in the design and development of vascular interventional devices from early stage to commercialization. Overall responsibility for technical aspects of new product development projects, including product specification generation and identification of optimal solution through design development, technical risk management and test capability development.
Responsibilities- Cross project ownership of device design and development, working with design engineers to identify novel solutions to meet product performance.
- Provide technical leadership and take ownership of critical technical tasks in the execution of product development projects.
- Design new products, optimise product performance and refine product design to meet technical specifications and unit cost target.
- Leading and developing project engineers, identifying and implementing best practice in the design and development of catheters
- Develop test capability to evaluate product performance and safety requirements.
- Identify and support development of processes for new products.
- Liaise with key opinion leaders to develop a deep understanding of the disease state, gather user needs; and articulate throughout the team.
- Attend external meetings with key opinion leaders to present the product portfolio and gain feedback on new product development.
- Strong technical leadership capability in the development of new products, expert understanding of disease state and generates creative product solutions to address unmet needs.
- Specific experience in cardiovascular, peripheral or neurovascular implants an advantage.
- Excellent technical problem solving and analytical ability.
- Strong device design, development and technical ability is essential, based on a solid foundation of fundamental engineering principles.
- Ability to communicate clearly, accurately, and directly, both verbally and in writing, to a widely varied audience.
- Creative problem solver.
- 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.
- 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.
- Excellent benefits.
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
This advertiser has chosen not to accept applicants from your region.
2
Senior Engineer , Research and 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.
Join embecta, a global leader in diabetes care, as Principal Engineer driving innovation across our product and technology development programs. This is a high-impact role where you'll lead complex engineering initiatives, mentor technical talent, and shape the future of healthcare solutions.
**Responsibilities**
+ Lead the development of novel technologies and product concepts that align with embecta's strategic roadmap.
+ Solve advanced technical challenges and ensure the success of R&D deliverables across multiple projects.
+ Manage technology budgets, resource planning, and cross-functional collaboration.
+ Drive innovation and process effectiveness while ensuring compliance with quality and safety standards.
+ Represent R&D in core team meetings and external engagements.
+ Mentor technical talent, promote continuous learning, and foster a culture of innovation.
+ Build partnerships with internal and external stakeholders to accelerate technology transfer and product development.
+ Promote inclusive collaboration and lead with courage and clarity in ambiguous environments.
**Experience and Education**
+ Bachelor's degree in Mechanical or Biomedical Engineering
+ 10+ years in product development, including 5+ years in medical devices.
+ Proven leadership in complex R&D programs.
+ Strong technical and organizational capabilities across:
+ **Execution & Planning** : Deliver milestones on time and budget.
+ **Risk & Budget Management** : Lead mitigation strategies and manage R&D budgets.
+ **Communication & Collaboration** : Foster cross-functional alignment and clarity.
+ **Analytical Thinking & Problem Solving** : Break down complex challenges and drive solutions.
+ **Customer Understanding & Product Architecture** : Translate user needs into impactful designs.
+ **Innovation & Initiative** : Champion new ideas and take ownership in ambiguity.
+ **Diversity & Inclusion** : Build inclusive teams and welcome diverse perspectives.
+ **Flexibility & Resilience** : Thrive in dynamic environments and adapt to change.
#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.
Join embecta, a global leader in diabetes care, as Principal Engineer driving innovation across our product and technology development programs. This is a high-impact role where you'll lead complex engineering initiatives, mentor technical talent, and shape the future of healthcare solutions.
**Responsibilities**
+ Lead the development of novel technologies and product concepts that align with embecta's strategic roadmap.
+ Solve advanced technical challenges and ensure the success of R&D deliverables across multiple projects.
+ Manage technology budgets, resource planning, and cross-functional collaboration.
+ Drive innovation and process effectiveness while ensuring compliance with quality and safety standards.
+ Represent R&D in core team meetings and external engagements.
+ Mentor technical talent, promote continuous learning, and foster a culture of innovation.
+ Build partnerships with internal and external stakeholders to accelerate technology transfer and product development.
+ Promote inclusive collaboration and lead with courage and clarity in ambiguous environments.
**Experience and Education**
+ Bachelor's degree in Mechanical or Biomedical Engineering
+ 10+ years in product development, including 5+ years in medical devices.
+ Proven leadership in complex R&D programs.
+ Strong technical and organizational capabilities across:
+ **Execution & Planning** : Deliver milestones on time and budget.
+ **Risk & Budget Management** : Lead mitigation strategies and manage R&D budgets.
+ **Communication & Collaboration** : Foster cross-functional alignment and clarity.
+ **Analytical Thinking & Problem Solving** : Break down complex challenges and drive solutions.
+ **Customer Understanding & Product Architecture** : Translate user needs into impactful designs.
+ **Innovation & Initiative** : Champion new ideas and take ownership in ambiguity.
+ **Diversity & Inclusion** : Build inclusive teams and welcome diverse perspectives.
+ **Flexibility & Resilience** : Thrive in dynamic environments and adapt to change.
#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.
3
Process Development Engineer
Cork, Munster
Meta
Posted 3 days ago
Job Viewed
Job Description
**Summary:**
At Meta Reality Labs, we are developing the future of Wearables and Mixed Reality products. This team focuses on developing µLED technologies for Meta products. We are seeking a Process Engineer to join our R&D team. In this role you will work closely with internal research teams, academic institutions, external partners and vendors. You will be the process/tool owner for a set of process tools known as the 'Back-End toolset' You will help define requirements and deliverables, schedule and track project progress. To be successful, you will eliminate barriers to your team's success, clearly communicate their work to all stakeholders. The successful candidate should demonstrated capacity to maintain high standards of quality and accuracy across multiple projects, demonstrated success in driving impact across stakeholders that have different perspectives or approaches and demonstrated experience of resourcefulness and adaptability in problem-solving and pivoting according to changes.
**Required Skills:**
Process Development Engineer Responsibilities:
1. Process ownership: process development and optimization for the back-end tools including but not limited to Bonding, CMP, Dice and grinding
2. Work cross-functionally with process development, device and process integration teams to define process requirements for micro-LED processes
3. Plan, execute, and analyze Design Of Experiments
4. Tool ownership: define tool configuration and acceptance criteria, selection, start-up, and qualifications
5. Establish, monitor, and maintain process tool controls
6. Develop and maintain Standard Operation Procedures, Out-of-Control Action Plan
7. Cross functional collaboration with industrial and academic partners
**Minimum Qualifications:**
Minimum Qualifications:
8. Bachelor's degree in Mechanical, Electrical, Materials, Physics, or Optics Engineering and/or equivalent experience
9. Experience with µLED processing with 2+ years hands-on experience
10. Understanding of µLED /semiconductor processing and integration
11. Experience with statistical process control (SPC setup and monitoring)
12. Experience with Design of Experiments 1+ years
**Preferred Qualifications:**
Preferred Qualifications:
13. Background in LED or micro-LED processing (GaN and Phosphide-based materials)
14. 3+ years of experience in research and manufacturing environments
15. Experience with root cause analysis, Failure Mode and Effects Analysis
16. Good communication skills
17. Problem-solving aptitude
18. Ability to work on ones own initiative with proven analytical and organizational skills
**Industry:** Internet
At Meta Reality Labs, we are developing the future of Wearables and Mixed Reality products. This team focuses on developing µLED technologies for Meta products. We are seeking a Process Engineer to join our R&D team. In this role you will work closely with internal research teams, academic institutions, external partners and vendors. You will be the process/tool owner for a set of process tools known as the 'Back-End toolset' You will help define requirements and deliverables, schedule and track project progress. To be successful, you will eliminate barriers to your team's success, clearly communicate their work to all stakeholders. The successful candidate should demonstrated capacity to maintain high standards of quality and accuracy across multiple projects, demonstrated success in driving impact across stakeholders that have different perspectives or approaches and demonstrated experience of resourcefulness and adaptability in problem-solving and pivoting according to changes.
**Required Skills:**
Process Development Engineer Responsibilities:
1. Process ownership: process development and optimization for the back-end tools including but not limited to Bonding, CMP, Dice and grinding
2. Work cross-functionally with process development, device and process integration teams to define process requirements for micro-LED processes
3. Plan, execute, and analyze Design Of Experiments
4. Tool ownership: define tool configuration and acceptance criteria, selection, start-up, and qualifications
5. Establish, monitor, and maintain process tool controls
6. Develop and maintain Standard Operation Procedures, Out-of-Control Action Plan
7. Cross functional collaboration with industrial and academic partners
**Minimum Qualifications:**
Minimum Qualifications:
8. Bachelor's degree in Mechanical, Electrical, Materials, Physics, or Optics Engineering and/or equivalent experience
9. Experience with µLED processing with 2+ years hands-on experience
10. Understanding of µLED /semiconductor processing and integration
11. Experience with statistical process control (SPC setup and monitoring)
12. Experience with Design of Experiments 1+ years
**Preferred Qualifications:**
Preferred Qualifications:
13. Background in LED or micro-LED processing (GaN and Phosphide-based materials)
14. 3+ years of experience in research and manufacturing environments
15. Experience with root cause analysis, Failure Mode and Effects Analysis
16. Good communication skills
17. Problem-solving aptitude
18. Ability to work on ones own initiative with proven analytical and organizational skills
**Industry:** Internet
This advertiser has chosen not to accept applicants from your region.
4
Software Development Engineer
Galway, Connacht
CVS Health Ireland
Posted today
Job Viewed
Job Description
CVS Health, the parent company of Signify Health, is increasing investments in digital, data, analytics and technology and Signify Health is excited to be involved! We are hiring for a dynamic new initiative for CVS Health that will run out of our state-of-the-art offices at Bonham Quay. This is your opportunity to be involved with a pioneering business that is transforming health care in the United States by making customer experiences more seamless, convenient and personalised. CVS Health is focused on driving business agility and growth through technology, data, digital and experiential innovations. 'Digital First, Technology Forward and Data Driven' is not simply an aspirational goal for the company, but a prerequisite to accelerated growth. Bring your heart to CVS Health. Every one of us at CVS Health shares a single, clear purpose: Bringing our heart to every moment of your health. This purpose guides our commitment to deliver enhanced human-centric health care for a rapidly changing world. Anchored in our brand - with heart at its center - our purpose sends a personal message that how we deliver our services is just as important as what we deliver. Our Heart At Work Behaviors support this purpose. We want everyone who works at CVS Health to feel empowered by the role they play in transforming our culture and accelerating our ability to innovate and deliver solutions to make health care more personal, convenient and affordable. As we reflect on our learnings and successes from remote work, we aim to provide a new state of the art flexible work environment in our Galway facility at Bonham Quay to support those objectives. Careers with offer flexible work arrangements and individuals who live and work in the Republic of Ireland will have the opportunity to divide their time between our Galway office and their home office. Position Summary The Retail Consumer Analytics team is helping lead the effort to transform and drive improved front store consumer experience by partnering with key business areas across CVS Health to deliver impactful analytic solutions and insights. As a member of the Analytics & Behavior Change Pricing Analytics team, you will deliver high visibility analytics projects for key CVS Retail strategic priorities. Within our team, we believe a cutting-edge AI product can only be delivered if every aspect of the solution from data to model to front end UI is fully designed and developed by SMEs within the team. As an Engineer, you will be joining a team designing, building, and delivering data science solutions for optimal retail pricing for CVS stores. Responsibilities include: You will drive revenue and customer satisfaction in CVS Health's Front Store business using advanced analytic solutions to optimizing merchandising and pricing decisions. You will solve complex problems and deliver decision support tools to improve customer experience. Collaborate with business stakeholders to understand business needs and convert them into requirements for solution enhancements or ad hoc analyses. Help guide the overall roadmap for enterprise optimal pricing solutions that deploy complex data science models through interactive user interfaces. Work with teams of data scientists, analysts, data engineers, and developers to execute both solution upgrades and analyses. Architect scalable and efficient data pipelines to ingest, transform, and analyze large volumes of structured and unstructured data within Palantir Foundry. Ensure compliance with best practices, security standards, and data governance policies throughout the development lifecycle. Provide technical guidance, mentorship, and support to junior developers and team members. Proactively identify opportunities for process improvements and optimization within Palantir Foundry ecosystem. We are a dynamic team focused on building innovative analytic solutions using AI/ML and cloud capabilities. We are looking for talented individuals who have a strong sense of ownership, accountability, and a desire to deliver high quality end to end intuitive and impactful analytic products using advanced data driven approaches. Required Qualifications 2+ years of software development experience building and delivering customer facing cloud-based analytic solutions 2+ years of end-to-end application development experience on Palantir foundry or similar systems, leveraging tools such as Workshop, Code Repositories, Pipeline Builder, Ontology objects/actions and Typescript functions Foundry applications or similar systems to meet business requirements and objectives. 2+ year of experience collaborating with cross-functional teams including data analysts, engineers, and business stakeholders to gather requirements and define project scope. 2+ years coding in Python/PySpark, SQL, and LLM modeling 2+ years in cloud-based platforms such as Azure, GCP and AWS. Preferred Qualifications 3+ years of software development experience building and delivering customer facing cloud-based analytic solutions 3+ years of experience leading the design, development, and deployment of applications on Palantir Foundry Platform Retail merchandising domain expertise including category management, assortment optimization, product clustering, product price sensitivity and promotion affinity evaluation, store clustering and localization Experience with Prompt Engineering developing solutions leveraging LLM models Education BA/BS degree required To Apply Please forward your CV via the APPLY Now button below.
This advertiser has chosen not to accept applicants from your region.
5
Product Development Engineer
Dublin, Leinster
Pale Blue Dot® Recruitment
Posted 13 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
This advertiser has chosen not to accept applicants from your region.
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6
Sr Software Development Engineer
Cork, Munster
Trellix
Posted 3 days ago
Job Viewed
Job Description
**_Job Title:_**
Sr Software Development Engineer
**About** **Trellix:**
**Trellix, the trusted CISO ally, is redefining the future of cybersecurity and soulful work.** Our comprehensive, GenAI-powered platform helps organizations confronted by today's most advanced threats gain confidence in the protection and resilience of their operations. Along with an extensive partner ecosystem, we accelerate technology innovation through artificial intelligence, automation, and analytics to empower over 53,000 customers with responsibly architected security solutions.
We also recognize the importance of closing the 4-million-person cybersecurity talent gap. We aim to create a home for anyone seeking a meaningful future in cybersecurity and look for candidates across industries to join us in soulful work. More at .
**_Role Overview:_**
We are looking for a passionate and experienced Senior Software Development Engineer to join our dynamic and fast-paced team. This role offers an opportunity to shape large-scale, automated test environments that directly impact Trellix's product quality and speed of delivery while engineering solutions for complex business challenges.
You'll be at the center of building services that support automated deployment and validation of our products. Your solutions will streamline our CI/CD pipeline and ensure our testing environments scale across tools, Trellix products, and platforms.
**Location: Cork - Hybrid**
**About the Role:**
+ Design, develop, and maintain robust, scalable, and high-performance software applications primarily using Groovy and C#.
+ Collaborate with global cross-functional teams across time zones to deliver impactful solutions that meet evolving product and QA needs.
+ Participate in architecture discussions and technical design reviews to improve system performance, reliability, and scalability.
+ Write efficient, maintainable code and unit tests that adhere to engineering best practices.
+ Create modular components with well defined APIs to enable flexible and easy integration into existing development infrastructures and workflows
+ Champion Agile best practices and contribute to continuous improvement in the software development lifecycle.
**Senior Software-specific:**
+ Identify and address technical debt and refactor existing codebase as necessary to improve system maintainability and scalability.
+ Conduct thorough code reviews, provide feedback, and help raise the quality bar for the entire team.
+ Proactively research and evaluate emerging technologies that can be leveraged for future development.
+ Influence architectural direction and technical strategy.
+ Drive open and effective communication across teams, helping guide decisions and technical alignment.
**About You:**
+ You have 5+ years of experience with a BS/BE in Computer Science, Computer Engineering or related field.
+ Proficiency in any of the following languages: Java or C#, or C++, with strong fundamentals in object-oriented design and design patterns.
+ Solid experience with VMware vSphere for managing and provisioning virtual infrastructure.
+ Experience with relational databases such as SQL Server or similar.
+ Familiarity with scripting languages such as PowerShell, Bash, or equivalent.
+ Working knowledge of Windows, Linux and Mac OS.
+ Ability to work both independently and collaboratively in a fast-paced environment.
+ Excellent problem solving and troubleshooting skills.
+ Working knowledge of cloud technologies, especially AWS and/or Google Cloud Platform (GCP).
+ Experience in Agile software development practices and Github for source control and collaboration.
+ Ability to collaborate and work with multiple teams across different time-zones.
+ Strong communication skills - able to articulate technical concepts to non-technical stakeholders and influence decisions.
+ Experience building enterprise-grade, distributed systems with a focus on performance, reliability, and scalability.
**_Company Benefits and Perks:_**
We believe that the best solutions are developed by teams who embrace each other's unique experiences, skills, and abilities. We work hard to create a dynamic workforce where we encourage everyone to bring their authentic selves to work every day. We offer a variety of social programs, flexible work hours and family-friendly benefits to all of our employees.
+ Retirement Plans
+ Medical, Dental and Vision Coverage
+ Paid Time Off
+ Paid Parental Leave
+ Support for Community Involvement
We're serious about our commitment to a workplace where everyone can thrive and contribute to our industry-leading products and customer support, which is why we prohibit discrimination and harassment based on race, color, religion, gender, national origin, age, disability, veteran status, marital status, pregnancy, gender expression or identity, sexual orientation or any other legally protected status.
Sr Software Development Engineer
**About** **Trellix:**
**Trellix, the trusted CISO ally, is redefining the future of cybersecurity and soulful work.** Our comprehensive, GenAI-powered platform helps organizations confronted by today's most advanced threats gain confidence in the protection and resilience of their operations. Along with an extensive partner ecosystem, we accelerate technology innovation through artificial intelligence, automation, and analytics to empower over 53,000 customers with responsibly architected security solutions.
We also recognize the importance of closing the 4-million-person cybersecurity talent gap. We aim to create a home for anyone seeking a meaningful future in cybersecurity and look for candidates across industries to join us in soulful work. More at .
**_Role Overview:_**
We are looking for a passionate and experienced Senior Software Development Engineer to join our dynamic and fast-paced team. This role offers an opportunity to shape large-scale, automated test environments that directly impact Trellix's product quality and speed of delivery while engineering solutions for complex business challenges.
You'll be at the center of building services that support automated deployment and validation of our products. Your solutions will streamline our CI/CD pipeline and ensure our testing environments scale across tools, Trellix products, and platforms.
**Location: Cork - Hybrid**
**About the Role:**
+ Design, develop, and maintain robust, scalable, and high-performance software applications primarily using Groovy and C#.
+ Collaborate with global cross-functional teams across time zones to deliver impactful solutions that meet evolving product and QA needs.
+ Participate in architecture discussions and technical design reviews to improve system performance, reliability, and scalability.
+ Write efficient, maintainable code and unit tests that adhere to engineering best practices.
+ Create modular components with well defined APIs to enable flexible and easy integration into existing development infrastructures and workflows
+ Champion Agile best practices and contribute to continuous improvement in the software development lifecycle.
**Senior Software-specific:**
+ Identify and address technical debt and refactor existing codebase as necessary to improve system maintainability and scalability.
+ Conduct thorough code reviews, provide feedback, and help raise the quality bar for the entire team.
+ Proactively research and evaluate emerging technologies that can be leveraged for future development.
+ Influence architectural direction and technical strategy.
+ Drive open and effective communication across teams, helping guide decisions and technical alignment.
**About You:**
+ You have 5+ years of experience with a BS/BE in Computer Science, Computer Engineering or related field.
+ Proficiency in any of the following languages: Java or C#, or C++, with strong fundamentals in object-oriented design and design patterns.
+ Solid experience with VMware vSphere for managing and provisioning virtual infrastructure.
+ Experience with relational databases such as SQL Server or similar.
+ Familiarity with scripting languages such as PowerShell, Bash, or equivalent.
+ Working knowledge of Windows, Linux and Mac OS.
+ Ability to work both independently and collaboratively in a fast-paced environment.
+ Excellent problem solving and troubleshooting skills.
+ Working knowledge of cloud technologies, especially AWS and/or Google Cloud Platform (GCP).
+ Experience in Agile software development practices and Github for source control and collaboration.
+ Ability to collaborate and work with multiple teams across different time-zones.
+ Strong communication skills - able to articulate technical concepts to non-technical stakeholders and influence decisions.
+ Experience building enterprise-grade, distributed systems with a focus on performance, reliability, and scalability.
**_Company Benefits and Perks:_**
We believe that the best solutions are developed by teams who embrace each other's unique experiences, skills, and abilities. We work hard to create a dynamic workforce where we encourage everyone to bring their authentic selves to work every day. We offer a variety of social programs, flexible work hours and family-friendly benefits to all of our employees.
+ Retirement Plans
+ Medical, Dental and Vision Coverage
+ Paid Time Off
+ Paid Parental Leave
+ Support for Community Involvement
We're serious about our commitment to a workplace where everyone can thrive and contribute to our industry-leading products and customer support, which is why we prohibit discrimination and harassment based on race, color, religion, gender, national origin, age, disability, veteran status, marital status, pregnancy, gender expression or identity, sexual orientation or any other legally protected status.
This advertiser has chosen not to accept applicants from your region.
7
Process Development Engineer Student
Wicklow, Leinster
Takeda Pharmaceuticals
Posted 3 days ago
Job Viewed
Job Description
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
Are you looking for a patient-oriented, innovation-driven company that inspires you and promotes your career? Then take your future in your hands and become part of Takeda as a
**_Process Development Engineer Student_**
The intern will gain experience in the pharmaceutical manufacturing industry within the Manufacturing Sciences Group. This role offers a unique opportunity to gain hands-on experience with cutting-edge analytical techniques in a dynamic, supportive team at Takeda's world-class facilities in Bray. Join us to develop your skills, contribute to life-changing medicines, and grow your career in an environment that values innovation, safety, and personal development.
**_How you will contribute_** **:**
+ Collaborate with the process engineers and compliance engineers on new product introduction (NPI) and process improvement projects;
+ Use statistical software packages in the identification and reporting of shifts, signals and trends in critical process parameters and product quality attributes;
+ Conduct production-based trials and studies, including in-process testing of product and creation of associated reports;
+ Creation of standard procedures for continuous improvement including non-value adding (NVA) analysis and redesign of existing standard Manufacturing Sciences procedures;
+ Preparation, review and/or execution of Risk Assessments, GMP assessments, Manufacturing Instructions, Annual Product Reviews and Validation Protocols / Reports;
+ Contribute to Technical Studies, Optimisation Studies, Process, Hold Time and Cleaning Validations;
+ Management of internal systems: requalification's, periodic reviews, sample orders, trial material, process recipes, Investigation & Test Plans, 5S, product sample management and Change Records.
In this position you will report to the **Process Development Engineer, Manufacturing Sciences Dept.**
**_What you bring to Takeda_** **:**
+ A self-starter with initiative and good interpersonal skills is required;
+ The applicant should also have excellent communication, report writing, time management skills and be highly IT proficient;
+ Attention to detail is also required to comply with the relevant industry and Company quality standards and the cGMP rules pertaining to production.
+ Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business;
+ Ensure timely completion of all SOP training and assessment;
+ Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.
+ Knowledge of the pharmaceutical industry and pharmaceutical Oral Solid Dosage (OSD) would be preferable but not essential.
**What Takeda can offer you:**
+ Flexible working arrangements
+ 26 vacation days plus additional days for service milestones
+ Employee Assistance Program
+ Wellbeing and engagement teams
+ Development opportunities
+ Coaching and mentoring
+ Humanitarian volunteering leave options
+ Subsidized canteen
+ Electric charging points available at parking locations
**More about us:**
Takeda is focused on creating better health for people and a brighter future for the world. We aim to discover and deliver life-transforming treatments in our core therapeutic and business areas, including gastrointestinal and inflammation, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines.
Takeda Ireland was established in 1997. Our story in Ireland is one of substantial growth, rapid change, and innovation. Over the past years, Takeda Ireland has invested over 55 million in Ireland to develop our manufacturing sites. Solidifying our commitment in our people and contributing to the local economy. Takeda in Ireland has commercial operations, corporate services, and manufacturing facilities across four locations: Baggot St, Bray, Citywest, and Grange Castle. We have been certified as Top Employer for several consecutive years.
**How we will support you:**
Takeda is proud of its commitment to create a diverse workforce and to provide equal employment opportunities to all employees and applicants for employment without regard to ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status or any other characteristic protected by law. If you are living with disabilities, chronic illness, or neurodiversity, please feel free to let us know so that we can provide you with appropriate support during the application process.
**Locations**
Bray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Paid Intern (Fixed Term) (Trainee)
**Time Type**
Full time
**Job Description**
Are you looking for a patient-oriented, innovation-driven company that inspires you and promotes your career? Then take your future in your hands and become part of Takeda as a
**_Process Development Engineer Student_**
The intern will gain experience in the pharmaceutical manufacturing industry within the Manufacturing Sciences Group. This role offers a unique opportunity to gain hands-on experience with cutting-edge analytical techniques in a dynamic, supportive team at Takeda's world-class facilities in Bray. Join us to develop your skills, contribute to life-changing medicines, and grow your career in an environment that values innovation, safety, and personal development.
**_How you will contribute_** **:**
+ Collaborate with the process engineers and compliance engineers on new product introduction (NPI) and process improvement projects;
+ Use statistical software packages in the identification and reporting of shifts, signals and trends in critical process parameters and product quality attributes;
+ Conduct production-based trials and studies, including in-process testing of product and creation of associated reports;
+ Creation of standard procedures for continuous improvement including non-value adding (NVA) analysis and redesign of existing standard Manufacturing Sciences procedures;
+ Preparation, review and/or execution of Risk Assessments, GMP assessments, Manufacturing Instructions, Annual Product Reviews and Validation Protocols / Reports;
+ Contribute to Technical Studies, Optimisation Studies, Process, Hold Time and Cleaning Validations;
+ Management of internal systems: requalification's, periodic reviews, sample orders, trial material, process recipes, Investigation & Test Plans, 5S, product sample management and Change Records.
In this position you will report to the **Process Development Engineer, Manufacturing Sciences Dept.**
**_What you bring to Takeda_** **:**
+ A self-starter with initiative and good interpersonal skills is required;
+ The applicant should also have excellent communication, report writing, time management skills and be highly IT proficient;
+ Attention to detail is also required to comply with the relevant industry and Company quality standards and the cGMP rules pertaining to production.
+ Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business;
+ Ensure timely completion of all SOP training and assessment;
+ Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.
+ Knowledge of the pharmaceutical industry and pharmaceutical Oral Solid Dosage (OSD) would be preferable but not essential.
**What Takeda can offer you:**
+ Flexible working arrangements
+ 26 vacation days plus additional days for service milestones
+ Employee Assistance Program
+ Wellbeing and engagement teams
+ Development opportunities
+ Coaching and mentoring
+ Humanitarian volunteering leave options
+ Subsidized canteen
+ Electric charging points available at parking locations
**More about us:**
Takeda is focused on creating better health for people and a brighter future for the world. We aim to discover and deliver life-transforming treatments in our core therapeutic and business areas, including gastrointestinal and inflammation, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines.
Takeda Ireland was established in 1997. Our story in Ireland is one of substantial growth, rapid change, and innovation. Over the past years, Takeda Ireland has invested over 55 million in Ireland to develop our manufacturing sites. Solidifying our commitment in our people and contributing to the local economy. Takeda in Ireland has commercial operations, corporate services, and manufacturing facilities across four locations: Baggot St, Bray, Citywest, and Grange Castle. We have been certified as Top Employer for several consecutive years.
**How we will support you:**
Takeda is proud of its commitment to create a diverse workforce and to provide equal employment opportunities to all employees and applicants for employment without regard to ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status or any other characteristic protected by law. If you are living with disabilities, chronic illness, or neurodiversity, please feel free to let us know so that we can provide you with appropriate support during the application process.
**Locations**
Bray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Paid Intern (Fixed Term) (Trainee)
**Time Type**
Full time
This advertiser has chosen not to accept applicants from your region.
8
Staff Process Development Engineer
Cork, Munster
Stryker
Posted 3 days ago
Job Viewed
Job Description
**Staff Process Development Engineer**
**23 months FTC**
**Position Summary**
Independently determines and develops approaches to a variety of technical problems of moderate scope and complexity.
Uses latest engineering techniques to reduce product time to market whilst adhering to regulatory requirements, project deadlines and product costs.
Builds productive internal and external working relationships and may periodically provide guidance and train other team members.
**What you will do:**
+ Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures.
+ Ensure quality of process and product as defined in the appropriate operation and material specifications.
+ Will select components and equipment based on analysis of specifications, reliability and regulatory requirements. Work with quality engineers to develop component specific testing and inspection protocols.
+ May lead/support capital acquisition activity from specifying equipment, contract negotiation, Installation and validation.
+ Will analyse equipment to establish operating data, conduct experimental test and result analysis. Lead and/or participate in process review meetings.
+ Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers and launches.
+ Complete capability studies for in process inspection and generate subsequent Inspection documentation.
+ Conduct MSA studies for new products and new processes.
+ Provide training for manufacturing team members.
+ Ensure adherence to GMP and safety procedures.
+ Review and approval of validation documentation.
+ All other duties as assigned.
**What you will need:**
+ B.S in Mechanical Engineering or related engineering discipline with 4 or more years' experience.
+ Proven track record of working in a team based environment.
+ Excellent Interpersonal Skills - able to express ideas and collaborate effectively with multidisciplinary teams. Be open minded with the ability to recognise good ideas.
+ Innovative thinker - should be able to envisage new and better ways of doing things.
+ Experience in executing complex problem solving techniques related to manufacturing/design technical issues. Good instincts and sound judgement for mechanical and structural design.
+ Good understanding of Design for Manufacturing (DFM), related statistical tools and validation/verification techniques.
+ Analytical skills, ability to plan, organise and implement concurrent tasks.
+ Good knowledge of manufacturing processes, materials, product and process design.
+ Be able to read and interpret complex engineering drawings and have the ability to understand geometrical dimensioning and tolerancing.
+ Experience in validation activities.
+ #IJ
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
**23 months FTC**
**Position Summary**
Independently determines and develops approaches to a variety of technical problems of moderate scope and complexity.
Uses latest engineering techniques to reduce product time to market whilst adhering to regulatory requirements, project deadlines and product costs.
Builds productive internal and external working relationships and may periodically provide guidance and train other team members.
**What you will do:**
+ Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures.
+ Ensure quality of process and product as defined in the appropriate operation and material specifications.
+ Will select components and equipment based on analysis of specifications, reliability and regulatory requirements. Work with quality engineers to develop component specific testing and inspection protocols.
+ May lead/support capital acquisition activity from specifying equipment, contract negotiation, Installation and validation.
+ Will analyse equipment to establish operating data, conduct experimental test and result analysis. Lead and/or participate in process review meetings.
+ Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers and launches.
+ Complete capability studies for in process inspection and generate subsequent Inspection documentation.
+ Conduct MSA studies for new products and new processes.
+ Provide training for manufacturing team members.
+ Ensure adherence to GMP and safety procedures.
+ Review and approval of validation documentation.
+ All other duties as assigned.
**What you will need:**
+ B.S in Mechanical Engineering or related engineering discipline with 4 or more years' experience.
+ Proven track record of working in a team based environment.
+ Excellent Interpersonal Skills - able to express ideas and collaborate effectively with multidisciplinary teams. Be open minded with the ability to recognise good ideas.
+ Innovative thinker - should be able to envisage new and better ways of doing things.
+ Experience in executing complex problem solving techniques related to manufacturing/design technical issues. Good instincts and sound judgement for mechanical and structural design.
+ Good understanding of Design for Manufacturing (DFM), related statistical tools and validation/verification techniques.
+ Analytical skills, ability to plan, organise and implement concurrent tasks.
+ Good knowledge of manufacturing processes, materials, product and process design.
+ Be able to read and interpret complex engineering drawings and have the ability to understand geometrical dimensioning and tolerancing.
+ Experience in validation activities.
+ #IJ
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
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