15 Research Development jobs in Ireland

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, IE013 Ballybritt Galway
**Job Description:**
**Johnson & Johnson MedTech** is seeking a **Research & Development Engineer** based in Galway, Ireland.
**Who are we?**
At Johnson & Johnson MedTech, 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 of the role**
You will play a pivotal role will play a key role in the development and support of innovative MedTech in a constantly evolving research field. This position involves supporting new indications for existing products, the development of new neurovascular MedTech products and supporting lifecycle management activities for commercialised products. You will work cross-functionally with internal teams and external partners to ensure robust product design, regulatory compliance, and effective implementation of product and process improvements.
**What to expect:**
Provide technical support for regulatory submissions and regional launches; and lead additional engineering studies as the need arises by regional authorities.
Support updates and improvements for existing products through design changes, process optimization, and technical investigations.
Build and update user documentation including procedures, protocols, reports and component specifications
Collaborate with and lead interfaces between cross-functional teams including Supply Chain, Regulatory Affairs, Quality Assurance and Manufacturing to ensure successful project execution.
Contribute to the project team to deliver key objectives while meeting performance, time and cost targets.
Assist in the development and execution of test methods and laboratory experiments.
Support feasibility studies, design verification and validation, and risk management in accordance with applicable regulatory standards.
Contribute to design and development activities for new neurovascular medical devices.
Develop a deep understanding of disease state and user techniques through engagement with physicians (Voice of Customer).
**Who are we looking for?**
Honours degree or equivalent experience in mechanical / biomedical engineering, or related field, with strong technical competence.
A proven ability in medical device design and development is required.
Design experience with SolidWorks
Excellent interpersonal skills and ability to work with people to achieve results.
Strong work ethic, creative problem solving, capable of working on own initiative.
Strong design and technical ability based on knowledge of fundamental engineering principles.
Excellent writing, presentation, and verbal communication skills essential.
Results and deadline driven with an ability to prioritise multiple tasks and operate in a fast-paced environment.
Highly motivated and a hardworking self-starter with the ability to work under own initiative and as a teammate.
Experience working in R&D in an established medical device manufacturer. Experience with neurovascular devices would be an advantage.
Experience in Life Cycle Management.
Experience working with chemistry / material science / liquid embolization products.
**What type of mark will** **YOU** **make?**
By joining **Johnson & Johnson** you will find boundless opportunities to craft your path & amplify your impact inside & outside our walls. And with our commitment to be the world's healthiest workforce you can strengthen your body as well and your mind. When you work at Johnson & Johnson you can touch over a Billion lives worldwide every day. And when you apply your talent to our collective purpose there's no end to the lasting impact we can make together. And that changes everything.

Overview The primary responsibility of this position is to support / lead on the design, development and taking to market of medical devices for Cook Medical. Reporting to: Team Lead, Research and Development / Manager, Research and Development Responsibilities Perform Duties of Research & Development Engineer 2: Design development, prototyping, test method design, design evaluation, design reviews, design specifications, design verification and validation, design protocols and reports, transfer to production activities in a timely effective manner. Product testing and evaluation, completion of test reports to support design selection. Preparation and presentation of design reviews. Product risk analysis and risk management. Contribute towards process development during introduction /development of new equipment and production processes as required for any new manufacturing techniques. Source new materials components and equipment. Development of component specifications, inspection methods, bills of materials and manufacturing processes. Introduction of new equipment, materials and technologies. As required work closely with Key Opinion Leaders, physicians, product managers and team to develop innovative medical devices to improve patient care. Work closely with Project Lead and take responsibility for assigned research and development project tasks: Manage and drive assigned project tasks to ensure timely completion of project milestones. Work closely with cross functional groups to achieve project and company goals. Product performance evaluations. Contribute to innovation and creativity within team through filing of disclosures and patents. Hold regular project meetings and document minutes and actions. Ensure project milestones are achieved to meet business metrics. Communications: Regular communication to cross-functional teams and senior management. Project status communications and reporting. Remain on the forefront of emerging industry practices. Educating oneself in the medical area for which the new devices are being developed in order to have an appreciation for what needs to be achieved with these products. Support other cross functional groups to deliver company goals. Ensure that Cook's Code of Conduct is considered in all business matters carried out on Cook's behalf. Qualifications Bachelor's degree is required, preferably in engineering or a related field. Minimum of 3 years' relevant experience is desired. Project planning/execution skills. Execution of project in a timely effective manner. Knowledge of anatomy and physiology. Good mechanical design and understanding of engineering fundamentals with medical device materials knowledge. Statistical understanding and experience. Manufacturing design and process understanding. Good working knowledge of Solidworks and/or Pro Engineer CAD. Strong technical writer. Knowledge of relevant ISO, EU, FDA medical device standards regulations is required. Willingness and availability to travel on company business. About Cook Limerick Cook Medical has been in Limerick since 1996, starting out with labeling and distribution and steadily growing and evolving to include manufacturing, centralised customer support and on to collaborative product development in the Innovation Centre. The Ireland location is our European headquarters and houses our EMEA Support Centre. This location currently employs more than 1000 people and manufactures 10% of Cook's products for global markets. Research and Development in Limerick Our mission with R&D is to invent, manufacture, and deliver a unique portfolio of medical devices to the healthcare systems of the world. Our R&D team in Limerick is split into two divisions, Vascular and Medsurg. The R&D engineering teams are responsible for bringing a product from idea or concept all the way to market launch. The MedSurg R&D team in Limerick has two programs, Endoscopy/EndoSurgery and Otolaryngology Head and Neck Surgery (OHNS) that it is responsible for designing and developing new and innovative products for. The R&D engineers and scientists have the opportunity to explore and create novel ideas within feasibility, bring a medical device through verification and validation phase and be a part of bringing a new product to the market. The MedSurg R&D team works in collaboration with Cook's sister site in Winston Salem, North Carolina. Our employee benefits include: Hybrid Work Model Company sponsored Defined Contribution pension scheme Medical Health Insurance cover for you and your immediate family Life Assurance and Income Protection cover Educational Assistance Performance related Bonus Extensive health & wellness program including Indian head massages, healthy lifestyle seminars, mindfulness courses, physio sessions, flu vaccinations, nutrition talks Fully equipped gym on site 39-hour week with flexible start & finish times Paid time off to participate in volunteer activities Free parking Subsidised restaurant Sports & Social club #LI-Hybrid To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process click the Continue to Application or Login/Register to apply button below.

Description
AWS Resilience owns service to prevent and response to availability and security issues for all AWS Services. In other words, we're the people who keep the cloud running. We work on the most challenging problems, with constant new services and possible failure modes to prevent - and we're looking for talented people who want to help.
You'll join a diverse team of software, security experts, operations managers, and other vital roles. You'll collaborate with people across AWS to help us deliver the highest standards for safety and security and availability. You'll experience an inclusive culture that welcomes bold ideas and empowers you to own them to completion.
AWS Incident Response is at the heart of the high availability of Amazon Web Services. We make customer impacting events shorter and less frequent by driving large scale event and incident response. Our automated tooling quickly identifies the cause of an issue and helps mitigate its impact, and much of our engineer time is spent on projects to improve the tooling and automation. We also provide manual incident management for AWS and other Amazon groups, directing the resolution of an issue with service teams, and diving deep into those events to drive improvements to the tooling. It's an exciting time to join our team as we are growing and expanding our offerings.
Key job responsibilities
You will own the organisation strategy relative to the usage of ML, GenAI and propose the best technology to advance our ability to better detect, faster root cause ,and correlate to prior incidents to shorten customer facing AWS incidents. Your work will enable us to identify gaps in our current strategy, learnings from past incidents. You will contribute to shortening incident response through deep analysis and introduction of new technology.
About the team
AWS Infrastructure Services (AIS)
AWS Infrastructure Services owns the design, planning, delivery, and operation of all AWS global infrastructure. In other words, we're the people who keep the cloud running. We support all AWS data centers and all of the servers, storage, networking, power, and cooling equipment that ensure our customers have continual access to the innovation they rely on. We work on the most challenging problems, with thousands of variables impacting the supply chain - and we're looking for talented people who want to help.
You'll join a diverse team of software, hardware, and network engineers, supply chain specialists, security experts, operations managers, and other vital roles. You'll collaborate with people across AWS to help us deliver the highest standards for safety and security while providing seemingly infinite capacity at the lowest possible cost for our customers. And you'll experience an inclusive culture that welcomes bold ideas and empowers you to own them to completion.
About AWS
Diverse Experiences
AWS values diverse experiences. Even if you do not meet all of the preferred qualifications and skills listed in the job description, we encourage candidates to apply. If your career is just starting, hasn't followed a traditional path, or includes alternative experiences, don't let it stop you from applying.
Why AWS?
Amazon Web Services (AWS) is the world's most comprehensive and broadly adopted cloud platform. We pioneered cloud computing and never stopped innovating - that's why customers from the most successful startups to Global 500 companies trust our robust suite of products and services to power their businesses.
Inclusive Team Culture
Here at AWS, it's in our nature to learn and be curious. Our employee-led affinity groups foster a culture of inclusion that empower us to be proud of our differences. Ongoing events and learning experiences, including our Conversations on Race and Ethnicity (CORE) and AmazeCon (gender diversity) conferences, inspire us to never stop embracing our uniqueness.
Mentorship & Career Growth
We're continuously raising our performance bar as we strive to become Earth's Best Employer. That's why you'll find endless knowledge-sharing, mentorship and other career-advancing resources here to help you develop into a better-rounded professional.
Work/Life Balance
We value work-life harmony. Achieving success at work should never come at the expense of sacrifices at home, which is why we strive for flexibility as part of our working culture. When we feel supported in the workplace and at home, there's nothing we can't achieve.
Basic Qualifications
- Masters degree (or European advanced degree equivalent) or PhD in Computer Science, or related technical, math, economics, or scientific field
- Several years of relevant experience in developing large scale machine learning or deep learning models and/or systems in a production environment
- Experience in using Python, R or Matlab or other statistical/machine learning software language
- Several year experience specifically with deep learning (e.g., CNN, RNN, LSTM, etc.)
- Experience hiring or mentoring more junior colleagues
Preferred Qualifications
- PhD degree in computer science, engineering, mathematics, economics, or related technical/scientific field
- Hands on experience building models with deep learning frameworks like PyTorch, or similar
- Experience with machine learning, time series, NLP and CV solutions
- Proven communication skills, presentation skills, and attention to detail
- Comfortable working in a fast paced, highly collaborative, dynamic work environment
- Scientific thinking and the ability to invent, a track record of thought leadership and contributions that have advanced the field.
Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a longstanding top priority for Amazon. Please consult our Privacy Notice ( ) to know more about how we collect, use and transfer the personal data of our candidates.
Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status.
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
**Job Description**
**Assoc Research Scientist - Biopharma**
At PPD, part of Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.
We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research, our work spans laboratory, digital and decentralized clinical trial services.
Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
We have a great opportunity for an Associate Research Scientist to join our growing Biopharmaceutical team. This role is a Technical Lead position based at our Analytical GMP facility in Athlone, Ireland.
**Location/Division Specific Information**
Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic guides. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.
**Discover Impactful Work:**
The role of Associate Research Scientist is responsible for the regulatory and scientific conduct of development and stability projects in the Biopharmaceutical Laboratory. Performs troubleshooting across multiple assay formats, clients and cell lines. Calculates and interprets data and records data in adherence with PPD SOPs and any additional requirements specific to the lab and/or client.
**A day in the life:**
+ Independently performs analytical testing, method optimization/validation, and/or other speciality technologies studies OR method transfers for pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or delivery systems. Understands and conforms to methods, and protocols applicable to assigned tasks. Designs and completes experiments independently.
+ Reviews and critiques study protocols, project status reports, final study reports and other project-related technical documents.
+ Prepares and reviews study protocols, project status reports, final study reports and other project-related technical documents.
+ Communicates data and technical issues to clients on a weekly basis (or as needed).
+ Provides technical mentorship and training to staff.
+ Leads analytical (procedural and instrumental) troubleshooting sessions.
+ Assists in preparation and implementation of SOPs and quality systems.
+ Reviews, interprets, and analyses data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.
**Education and Experience**
+ Degree or equivalent in Chemistry or Biochemistry
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
+ Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
**Knowledge, Skills, Abilities**
+ Knowledge of general chemistry, biochemistry techniques (Western Blot, total protein by BCA or micro BCA assay, ELISA, HPLC/UPLC)
+ Proven experience of method development of identity and purity assays by Western Blot.
+ Ideally experience in leading CMC studies for biopharmaceutical products including method validation
+ Proficiency on technical operating systems (including Image Lab software)
+ Proven problem solving and troubleshooting abilities
+ Ability to independently perform root cause analysis for method investigations
+ Proven ability in technical writing skills
+ Time management and project management skills
+ Good written and oral communication skills
+ Ability to work in a collaborative work environment with a team
+ Ability to train junior staff
**Work Environment**
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
+ Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
+ Able to work upright and stationary and/or standing for typical working hours.
+ Able to lift and move objects up to 25 pounds.
+ Able to work in non-traditional work environments.
+ Able to use and learn standard office equipment and technology with proficiency.
+ May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
+ Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today!** ** Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
**Accessibility/Disability Access**
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1- *. Please include your contact information and specific details about your required accommodation to support you during the job application process.
+ This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.
**_We welcome and encourage applicants from outside of Ireland. We can provide support with immigration and visa needs for successful applicants and dependents, tax consultations and other basic destination services. All other relocation costs are at the expense of the applicant._**
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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

Job Opportunity at Keohane Seafoods At Keohane Seafoods, our mission is to provide, consistent, high-quality seafood year-round. We create the products our customers ask for and make it easy with convenient formats that are easy to prepare. Our products honour the best the ocean has to offer and deliver the topmost value to our customers. Job Summary The successful candidate will join a dynamic team that develops branded and private label seafood products for the Irish & European retail market. The role involves working closely with the Technical, Production and Market & Sales departments to launch high quality added value seafood products. Working with a team of technical & commercial professionals, you will get involved in the latest innovation projects, ensuring new products are technically safe and legal with the correct specifications. To succeed in this role, you will need a culinary arts/food technology/science background and be able to apply your knowledge in a commercial setting. Key Responsibilities Ensuring all new products are consistently delivering for the consumer while meeting the agreed standards for the product To take lead and assist on NPD & EPD projects through the NPD process for concept to Launch, working cross functionally to deliver innovation and renovation projects. Ensuring 100% compliance with all policies and legislation Coordinate the day to day NPD process of line extension and brand pack -resizing projects from project brief, right through to launch Monitoring compliance with stage gate product development process and implementing Lean NPD techniques Ensuring that the Process and Product are protected and continuously improved Developing a clear and concise understanding of the business priorities and playing a vital part in delivering the guiding principle of lowest cost Liaising with Key Account Retail Customers and delivering NPD projects at Customer meetings. Contributing to, and taking lead on innovative NPD Projects Experience Required A Third level degree in Food Technology, Food Science or Food Business 3+ years hands on experience in the FMCG sector/food manufacturing environment in a transferable role such as Quality/ Technical/ Development Functional experience in: Quality systems e.g. BRC Standard, HACCP systems, Allergen control, ETC Supplier and product selection. Product quality optimisation Skills: Innovation

As part of Quality Tractor Parts Ltd. strategic growth and expansion plan a New Product Development Specialistis required.This is a full-time permanent role with a competitive salary based on experience. You will report to Head of Supply Chain. Duties Develop new products and services intended to assist in strategic planning. Gathering and analysing market research data. Monitor market trends and information collected by sales team to identify potential products for the development of new portfolio, and the restructuring of existing products. Take new and modified commercial lines products from concept to implementation across all lines of business for the target market. Remain current on market trends, product positioning, successes and competition and recommend appropriate actions based on analysis. Provide regular feedback on product requirements for foreign markets, including product specifications functionality, pricing, and translation needs. Prepare and execute local product launches and report on expectations of market size, market uptake, market share and expected budgeted sales. Define product promotion and positioning for defined segments. Produce financial analyses, projections, based on these proposed solutions. Define customer segmentation and target groups. Assess customer needs and requirements for defined segments and target accordingly. Candidate Profile Agri Machinery market knowledge a distinct advantage. Project Management experience with an Ability to establish credibility and rapport with all stakeholders. Degree level with focus on Mechanical Engineering, Business administration or NPD Familiarity with all aspects of product development and launches. 2-4 years experience in project planning and management 2-4 years experience in New Product Development Skills: Product Development Product Knowledge Project Management Agri Machinery Market Research Benefits: Pension Fund Parking Death in Service

Product Development Specialist - German Market Location: Dublin or Market-Based | Industry: Insurance | Language Requirement: Native German, Fluent English A leading international insurance company is seeking a Product Development Specialist to join its growing Commercial Division, focused on the German and Austrian markets. This is a key role in shaping innovative product propositions and enhancing an extensive insurance product portfolio. You must be fluent in German, as the position is focussed on developing insurance products & solutions for the German & Austrian Markets. Key Responsibilities: Develop and enhance insurance products for the German and Austrian markets. Draft, review, and manage policy wordings and customer-facing documentation (T&Cs, IPIDs, certificates, etc.) ensuring both clarity and technical accuracy. Propose and implement product improvements and changes to strengthen market offerings. Lead internal processes for documentation standards and technical content improvements. Collaborate with cross-functional teams to design product concepts, prepare briefs, and support product lifecycle management. Conduct market research, competitive analysis, and customer insights to inform product development. Prepare internal documentation for product sign-offs and present findings to senior stakeholders. Provide technical expertise to support sales, marketing, and training efforts. Contribute to overall product strategy, innovation, and regulatory alignment. Key Skills & Experience Sought: Native-level German with fluent English (both written and spoken). Strong background in insurance product development (life or non-life). Proven experience drafting and managing insurance policy documents and customer materials. Familiarity with insurance regulation and compliance in Germany and/or Austria. Strong command of MS Office; experience with Adobe InDesign is an advantage. Analytical thinker with high attention to detail. Comfortable presenting complex information clearly to stakeholders. Able to manage deadlines and adapt in a fast-paced, evolving environment. Self-starter with the ability to work independently and as part of a team. Must have Insurance / Financial Services industry experience What else is on offer: A key role in a respected, global insurance business Hybrid working flexibility Opportunity to work on innovative insurance solutions for the DACH region Collaborative, international work environment with career development potential If you're a detail-oriented insurance professional with a passion for product innovation and fluency in German, apply now to join a market leader shaping the future of insurance in the DACH region. Salary: €55-65K + benefits Hybrid work environment - Dublin based office Although a hybrid role, YOU MUST be living & based in Ireland for the duration of this role. NO SPONSORSHIP provided, so You MUST hold EU/EEA citizenship or a valid Irish work visa already. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy. Skills: Product Development Specialist - German Market Insurance German fluent Benefits: + excellent benefits

Job Description We are seeking an experienced Programme Manager to lead our New Product Development initiatives in Ballina, Ireland. This pivotal role will drive innovation and guide cross-functional teams through the entire product development lifecycle, from concept to launch. Develop and implement comprehensive programme plans for NPD projects, aligning with organisational goals and strategies Lead and motivate cross-functional teams, fostering a collaborative and innovative environment Manage programme budgets, timelines, and resources, ensuring efficient allocation and utilisation Identify and mitigate risks throughout the product development process, implementing effective solutions Collaborate with customers at all levels, including senior management, to ensure programme success and alignment with business objectives Oversee the product development lifecycle, from ideation to market launch, ensuring quality and timely delivery Analyse market trends and customer feedback to inform product development strategies Establish and monitor key metrics to measure programme success and drive continuous improvement Present regular progress reports and updates to senior management and key partners. Facilitate effective communication and knowledge sharing across teams and departments Qualifications Bachelor's degree in Engineering, Business Administration, or a related field Minimum 5-7 years of experience in programme management or product development roles Proven track record of successfully delivering complex projects or programmes Strong knowledge of project management methodologies (e.g., Agile, Scrum, Waterfall) Expertise in product development lifecycle management Proficiency in budgeting, financial planning, and risk management Excellent stakeholder management and communication skills Advanced problem-solving and decision-making abilities Proficiency in project management software (e.g., Microsoft Project, Jira) Experience in leading and motivating cross-functional teams In-depth understanding of industry trends and best practices in NPD Knowledge of manufacturing processes and supply chain management (depending on the industry) Project Management Professional (PMP) certification or equivalent is preferred Demonstrated ability to work effectively in a fast-paced, dynamic environment Strong analytical skills with a meticulous approach Additional Information LGC is a top life science tools company, offering important solutions in growing markets. Our values PASSION CURIOSITY INTEGRITY BRILLIANCE RESPECT Benefits 25 days holidays Life assurance & health allowance Discounts with local and national retailers Free 24/7 Employee Assistance Programme Recognition schemes and monetary awards Great long-term career opportunities At LGC, we foster a culture of inclusion and collaboration. We believe that diverse perspectives lead to better outcomes and encourage applicants from all backgrounds to apply. We are an equal opportunity employer and offer reasonable accommodations to individuals with disabilities. If you require any adjustments throughout the recruitment process, please let us know. Join us in this unique opportunity to be part of a company that is leading advancements in the industry! #lgcij To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.