12 New Product Development jobs in Ireland

Product Development Engineer

Dublin, Leinster Pale Blue Dot® Recruitment

Posted 8 days ago

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Job Description

full-time permanent

Product Development Engineer – Medical Device Industry

We are seeking a highly skilled and motivated Product Development Engineer to join a fast-paced and innovative medical device team. This role is central to the design, development, and optimization of next-generation medical technologies, involving both hardware and software components. You will work cross-functionally to bring products from concept through to commercialization, ensuring compliance with regulatory standards and a strong focus on patient outcomes.

Responsibilities Include but are not Limited to:

  • Lead product development activities from design and prototyping to testing, validation, and market launch.

  • Collaborate with Operations, QA/RA, Technical Support, and Commercial teams to ensure smooth and compliant product development.

  • Partner with Product Management to define product strategies and technical requirements aligned with business goals.

  • Define design inputs, conduct feasibility studies, and contribute to the development of technical documentation including design history files and technical files.

  • Work on embedded systems, firmware, and software development to support fully integrated device functionality.

  • Conduct risk assessments and support the implementation of risk management strategies.

  • Optimize designs for manufacturability, scalability, and performance.

  • Manage the full product development lifecycle and ensure adherence to regulatory and quality requirements.

  • Participate in design reviews and prototype evaluations, offering technical guidance across departments.

  • Troubleshoot and resolve product issues during both development and post-market stages.

  • Degree in Engineering (Biomedical, Mechanical, Electrical, or a related discipline).

  • Minimum of 5 years' experience in product development, preferably in the medical device sector or a closely related field.

  • Strong experience with embedded systems, firmware, and software development.

  • Proven background in taking medical devices from concept to market launch.

  • Solid understanding of design controls, validation, and regulatory compliance (e.g., FDA, ISO 13485).

  • Proficient in both hardware and software product design, prototyping, and testing.

  • Knowledge of mechanical engineering principles, manufacturing processes, and materials.

  • Familiar with risk management techniques (e.g., FMEA) and regulatory documentation practices.

  • Skilled in CAD tools (e.g., SolidWorks, AutoCAD), MATLAB, C/C++, Python, and embedded platforms.

Core Competencies:

  • Strong analytical, problem-solving, and decision-making skills.

  • Excellent communication skills, both verbal and written.

  • Proven ability to work cross-functionally with engineering, regulatory, quality, and commercial teams.

  • Highly detail-oriented, proactive, and adaptable with a continuous improvement mindset.

Preferred & Desirable Qualifications:

  • Experience with auditory or wearable medical technologies.

  • Familiarity with FDA 21 CFR Part 820, ISO 13485, ISO 14971 standards.

  • Experience with PLM systems and product lifecycle documentation.

  • Lean/Six Sigma or other continuous improvement methodologies.

  • Ability to mentor and train junior team members.

  • Track record of process and product optimization with risk mitigation.

  • Flexibility to work in a dynamic and evolving environment.

  • Willingness to travel internationally as required.

Note: By applying for this position, you may also be considered by Pale Blue Dot® Recruitment for other or future related vacancies.

 Pale Blue Dot® Recruitment

The Experts in STEM Workforce Solutions

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Senior Product Development Engineer

Galway, Connacht Life Science Recruitment Ltd

Posted today

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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
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Senior product development engineer

Galway, Connacht Life Science Recruitment Ltd

Posted today

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Job Description

permanent
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
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New Product Development Technologist (Food)

Monaghan, Ulster Ascension

Posted today

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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
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New product development technologist (food)

Monaghan, Ulster Ascension Executive

Posted today

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Job Description

permanent
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
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Associate Director, Pen Injector Product Development

Dún Laoghaire, Leinster embecta

Posted today

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Job Description

embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. For more information, visit  embecta.com  or follow our social channels on  LinkedIn ,  Facebook ,  Instagram  and X ( . 
**Why join us?**
A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work.  Here our employees can fulfill their life's purpose through the work that they do every day.
You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture.  Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees.
embecta, formerly part of BD, is one of the largest pure-play diabetes care companies in the world, leveraging its nearly 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships, and the passion of more than 2,000 employees around the globe.
This role leads the development of core technologies within R&D, guiding strategic direction across innovation projects. You'll evaluate emerging trends, advise on future technology choices, and help build lasting technical expertise to drive product advancement.
**Responsibilities**
+ Partner with key stakeholders across the various functions, to align objectives by understanding market opportunities, strategic goals and roadmaps
+ Develop, implement, and coordinate strategies as they relate to Pen Injectors and Auto Injectors
+ Understand the current market landscape of pen injectors and auto injectors, their strengths and weaknesses and associated opportunities for embecta.
+ Ensure that all new products are Designed For high volume Manufacturing and Assembly (DFMA)
+ Followsdesign, quality,and safetyguidelinesbasedonGMP, FDA, andISOguidelinesand relatedembecta Quality and Safety Standards and Practices
+ Leads and motivates a lean, high performing team in the development of new products that increase revenue for embecta with a short payback period and quick launch windows.
+ Leverage the Engineering Group in Dún Laoghaire, Ireland in alignment with the Director of the Engineering Group.
+ Bring an exciting energy to the Dún Laoghaire team, identifying high potential candidates for development and possible rotation through the Pen Injector Development Team.
**Education and Experience**
+ Bachelor's degree in Mechanical Engineering or related technical field is required; advanced degree is a plus
+ Minimum of 15 years relevant experience in successful cross-functional matrix organizations
+ 10+ years of experience in medical industries developing mechanical-based consumable Medical Devices
+ Experience working with and managing internal talent, as well as third-party consultants and service providers
+ Excellent presentation and communication skills, including executive presentation
+ Superior analytical, evaluative, and problem-solving abilities
#LI-HYBRID
#LI-DF1
embecta is an Equal Opportunity/Affirmative Action Employer.  We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
This advertiser has chosen not to accept applicants from your region.

Associate Director, Pen Injector Product Development

Dublin, Leinster Embecta

Posted today

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Job Description

embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. embecta, formerly part of BD, is one of the largest pure-play diabetes care companies in the world, leveraging its nearly 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships, and the passion of more than 2,000 employees around the globe. This role leads the development of core technologies within R&D, guiding strategic direction across innovation projects. You'll evaluate emerging trends, advise on future technology choices, and help build lasting technical expertise to drive product advancement. Responsibilities Partner with key stakeholders across the various functions, to align objectives by understanding market opportunities, strategic goals and roadmaps Develop, implement, and coordinate strategies as they relate to Pen Injectors and Auto Injectors Understand the current market landscape of pen injectors and auto injectors, their strengths and weaknesses and associated opportunities for embecta. Ensure that all new products are Designed For high volume Manufacturing and Assembly (DFMA) Follows design, quality, and safety guidelines based on GMP, FDA, and ISO guidelines and related embecta Quality and Safety Standards and Practices Leads and motivates a lean, high performing team in the development of new products that increase revenue for embecta with a short payback period and quick launch windows. Leverage the Engineering Group in Dn Laoghaire, Ireland in alignment with the Director of the Engineering Group. Bring an exciting energy to the Dn Laoghaire team, identifying high potential candidates for development and possible rotation through the Pen Injector Development Team. Education and Experience Bachelor's degree in Mechanical Engineering or related technical field is required; advanced degree is a plus Minimum of 15 years relevant experience in successful cross-functional matrix organizations 10+ years of experience in medical industries developing mechanical-based consumable Medical Devices Experience working with and managing internal talent, as well as third-party consultants and service providers Excellent presentation and communication skills, including executive presentation Superior analytical, evaluative, and problem-solving abilities #LI-HYBRID #LI-DF1 embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
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Associate Director Pen Injector Product Development

Dublin, Leinster Collins McNicholas

Posted today

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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
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Associate director, pen injector product development

Dublin, Leinster Embecta

Posted today

Job Viewed

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Job Description

permanent
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.
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Manager, Product Design, Impact

Dublin, Leinster ServiceNow, Inc.

Posted today

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It all started in sunny San Diego, California in 2004 when a visionary engineer, Fred Luddy, saw the potential to transform how we work. Fast forward to today - ServiceNow stands as a global market leader, bringing innovative AI-enhanced technology to over 8,100 customers, including 85% of the Fortune 500®. Our intelligent cloud-based platform seamlessly connects people, systems, and processes to empower organizations to find smarter, faster, and better ways to work. But this is just the beginning of our journey. Join us as we pursue our purpose to make the world work better for everyone.
**Team & Role**
At ServiceNow, we embrace representation in and from all professional and personal backgrounds and cultures. This diversity inspires passion and creativity among our teams and propels innovation in our products.
At ServiceNow, our Product Design team uses their superpower of empathizing, understanding, and applying our users' and customers' needs, with the mission to create product experiences they love. Our designers come from a diverse set of skills and backgrounds - design systems, visual, interaction, content, and product design. At ServiceNow, design has a very intentional seat at the table, so our team collaborates closely with both engineering and product management from the get-go.
Learn more about our team here the Impact team, we help customers realize value faster, adopt with ease, maintain platform health, and scale confidently-with expert guidance, AI agents, and continuous support. Designers here shape experiences that make complex tools simple, intuitive, and actionable for customers. The work directly influences how global enterprises engage with and succeed on ServiceNow.
**What you get to do in this role:**
+ Lead a team of product designers (junior to staff level) across established product areas, building on strong foundations while driving innovation and usability improvements.
+ Act as a player-coach: mentor designers in craft, critique, and problem-solving, while being comfortable stepping into design execution when needed to unblock the team.
+ Drive the UX vision and execution of a platform that supports and enhances ServiceNow's product line-simplifying complex, technical systems into clear and compelling user experiences.
+ Hold a sharp eye for design quality, raising the bar on execution in Figma and ensuring consistent, high-standard experiences across your team's work.
+ Navigate ambiguity and teach your team how to do the same-turning complex, technical, or uncertain product challenges into clear priorities and actionable paths forward.
+ Collaborate cross-functionally with product management, user research, engineering, and content, from strategic definition and planning through tactical execution of product roadmaps.
+ Inspire and guide your team, collaborate with peer managers across product areas, and communicate progress and strategy upward to VP/SVP leaders with clarity.
+ Translate complex enterprise and technical systems into simple, compelling stories-helping cross-functional partners, executives, and customers quickly understand the value of design decisions.
+ Evangelize design strategy and product vision across distributed design and product teams, while connecting design strategy to business strategy to influence priorities and outcomes.
**Preferred Qualifications: **
+ Experience in leveraging or critically thinking about how to integrate AI into work processes, decision-making, or problem-solving. This may include using AI-powered tools, automating workflows, analyzing AI-driven insights, or exploring AI's potential impact on the function or industry.
+ 8+ years of experience in UX/Product Design, with a strong portfolio demonstrating enterprise or technical design work.
+ 3+ years of experience managing and growing designers, with proven ability to coach, critique, and hold a high bar for design quality.
+ Hands-on design skills in Figma (or similar), with the ability to guide craft execution and step into design work when needed.
+ Experience leveraging or applying AI/ML to enhance product processes and workflows, or designing AI-native product experiences.
+ Strong storytelling skills-capable of translating complex, technical systems into clear, persuasive narratives for executives, peers, and customers.
+ Ability to navigate ambiguity, break down complex problems into clear priorities, and teach teams how to do the same.
+ Excellent communication, collaboration, and influence skills, with experience engaging 360°: upwards with execs, sideways with peers, and downwards with direct reports.
+ Demonstrated ability to connect design strategy with business strategy, advocating for users while driving measurable product outcomes.
+ Expected to demonstrate a high level of initiative, good sense of humor, and a "make it work" ethos
**Basic Qualifications:**
+ BA/BS degree or higher in Design, Design Communication, Human-Computer Interaction, or equivalent combination of education and experience in other related fields.
+ Experience participating in the complete product development lifecycle of web and/or software applications.
+ Experience in user experience design or industry experience (corporate, software, web or agency).
#UXD
**Work Personas**
We approach our distributed world of work with flexibility and trust. Work personas (flexible, remote, or required in office) are categories that are assigned to ServiceNow employees depending on the nature of their work and their assigned work location. Learn more here ( . To determine eligibility for a work persona, ServiceNow may confirm the distance between your primary residence and the closest ServiceNow office using a third-party service.
**Equal Opportunity Employer**
ServiceNow is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, sex, sexual orientation, national origin or nationality, ancestry, age, disability, gender identity or expression, marital status, veteran status, or any other category protected by law. In addition, all qualified applicants with arrest or conviction records will be considered for employment in accordance with legal requirements.
**Accommodations**
We strive to create an accessible and inclusive experience for all candidates. If you require a reasonable accommodation to complete any part of the application process, or are unable to use this online application and need an alternative method to apply, please contact for assistance.
**Export Control Regulations**
For positions requiring access to controlled technology subject to export control regulations, including the U.S. Export Administration Regulations (EAR), ServiceNow may be required to obtain export control approval from government authorities for certain individuals. All employment is contingent upon ServiceNow obtaining any export license or other approval that may be required by relevant export control authorities.
From Fortune. ©2025 Fortune Media IP Limited. All rights reserved. Used under license.
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  58. person_search Recruitment Consultancy
  59. store Retail
  60. point_of_sale Sales
  61. science Scientific Research & Development
  62. wifi Telecoms
  63. psychology Therapy
  64. pets Veterinary
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