184 Product Engineer jobs in Ireland

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.
The Lead Product Engineer will be an integral part of the product lifecycle engineering team responsible for supporting the various product lines in the $1 Billion embecta diabetes business. The Lead Product Engineer's primary role would be to provide support on a global basis for Product Engineering working closely with product development, regulatory affairs, marketing, operations, manufacturing plants, and quality utilizing the support of a small team of engineers.
**_RESPONSIBILITIES:_**
+ Utilizing best-in class project management practices, plan and execute product lifecycle engineering R&D projects which impact form/fit/function, business growth, cost reduction and compliance.
+ Lead engineering projects through embecta's change control processes.
+ Communicate project updates and escalations as appropriate to line management and to cross functional stakeholders within the embecta business.
+ Ensure compliance with all local, international and embecta quality and safety regulations, policies, and procedures.
+ Collaborate with manufacturing plants to assist in problem solving and issue resolution.
+ Augment and maintain robust design history files for the current diabetes products and line extensions.
+ Plan and conduct ongoing competitive product analysis and device compatibility testing to provide key insights into the competitive landscape and device compatibility.
+ Design test equipment and create validated test procedures for product testing to demonstrate compliance with internal and external requirements, such as ISO standards.
+ Manage, coach, and mentor junior product engineers as appropriate.
**_EXPERIENCE & EDUCATION:_**
+ Bachelor's degree in Engineering or Science, preferably in Mechanical, Biomedical, or Chemical Engineering.
+ Project Management qualification an advantage
+ 10+ years' experience in medical device design or R&D with a successful track record of delivering products to market and successfully supporting products in the market after launch
+ Experience leading technical resources
+ Practical experience with implementing product changes through a structured, phase-gated product development process within a regulated framework
+ Experience in technical Problem Solving
+ Medical product design, research, and development.
+ High volume manufacturing desired
+ Polymer material science and injection molding processes.
+ GD&T 3D CAD modeling.
+ Statistical analysis
+ Project management
**KNOWLEDGE, SKILLS AND ABILITIES:**
+ Leadership and team building skills
+ Disciplined and well organized
+ Ability to manage competing simultaneous priorities effectively
+ Ability to clearly communicate ideas and knowledge to other individuals and teams - both in writing and verbally
+ Demonstrated deep understanding of establishing project and product requirements
+ Highly collaborative both within the function and with other functions
+ Advanced technical and managerial judgment; advanced problem-solving skills
+ Self-initiator, results driven and action & detail oriented
embecta is an Equal Opportunity/Affirmative Action Employer.  We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. The Lead Product Engineer will be an integral part of the product lifecycle engineering team responsible for supporting the various product lines in the $1 Billion embecta diabetes business. The Lead Product Engineer's primary role would be to provide support on a global basis for Product Engineering working closely with product development, regulatory affairs, marketing, operations, manufacturing plants, and quality utilizing the support of a small team of engineers. RESPONSIBILITIES: Utilizing best-in class project management practices, plan and execute product lifecycle engineering R&D projects which impact form/fit/function, business growth, cost reduction and compliance. Lead engineering projects through embecta's change control processes. Communicate project updates and escalations as appropriate to line management and to cross functional stakeholders within the embecta business. Ensure compliance with all local, international and embecta quality and safety regulations, policies, and procedures. Collaborate with manufacturing plants to assist in problem solving and issue resolution. Augment and maintain robust design history files for the current diabetes products and line extensions. Plan and conduct ongoing competitive product analysis and device compatibility testing to provide key insights into the competitive landscape and device compatibility. Design test equipment and create validated test procedures for product testing to demonstrate compliance with internal and external requirements, such as ISO standards. Manage, coach, and mentor junior product engineers as appropriate. EXPERIENCE & EDUCATION: Bachelor's degree in Engineering or Science, preferably in Mechanical, Biomedical, or Chemical Engineering. Project Management qualification an advantage 10+ years' experience in medical device design or R&D with a successful track record of delivering products to market and successfully supporting products in the market after launch Experience leading technical resources Practical experience with implementing product changes through a structured, phase-gated product development process within a regulated framework Experience in technical Problem Solving Medical product design, research, and development. High volume manufacturing desired Polymer material science and injection molding processes. GD&T 3D CAD modeling. Statistical analysis Project management KNOWLEDGE, SKILLS AND ABILITIES: Leadership and team building skills Disciplined and well organized Ability to manage competing simultaneous priorities effectively Ability to clearly communicate ideas and knowledge to other individuals and teams - both in writing and verbally Demonstrated deep understanding of establishing project and product requirements Highly collaborative both within the function and with other functions Advanced technical and managerial judgment; advanced problem-solving skills Self-initiator, results driven and action & detail oriented embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. The Product Engineer will be an integral part of the product lifecycle engineering team responsible for supporting the various product lines in the $1 Billion embecta diabetes business. The Product Engineer's primary role would be to provide support on a global basis for Product Engineering, working closely with regulatory affairs, marketing, operations, manufacturing plants, and quality Support engineering projects through embecta's change control processes. Write protocols and execute testing to support product changes . Communicate project updates and escalations as appropriate to line management and to cross functional stakeholders within the embecta business. Conduct competitive product analysis and device compatibility testing to provide key insights into the competitive landscape and device compatibility. Collaborate with manufacturing plants to assist in problem solving and issue resolution. Design test equipment and validate test procedures for product testing . Augment and maintain robust design history files for the current diabetes products and line extensions. Ensure compliance with all local, international and embecta quality and safety regulations, policies, and procedures. Education Bachelor's degree in Engineering or Science, preferably in Mechanical, Biomedical, or Chemical Engineering Project Management qualification an advantage 3+ years' experience in medical device design or R&D with a successful track record of delivering products to market and successfully supporting products in the market after launch. Medical product design, research, and development. Exposure to high volume manufacturing desired. Polymer material science and injection moulding processes desired. Design verification GD&T 3D CAD modeling. Statistical analysis Test method validation Project management Fixed Term Contract (Fixed Term) 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.

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 Description Summary**
This position is for a Security Engineering role within BD's Product Security Organisation. The future candidate would be responsible for/supporting the Inffusion OUS portfolio, including projects like BD neXus and the BD Infusion legacy portfolio. The candidate should be strong in software documentation and technical security aspects.
**Job Description**
**We are the makers of possible**
BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
**Why join us?**
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
Become a **maker of possible** with us!
**Our vision for Medication Management Solutions at BD**
With our technical capabilities, the Medication Management Solutions (MMS) team are able to manage multiple systems and our operational capabilities enable us to have medications available when and where needed, reducing inefficiency and waste for nursing and pharmacy teams.
**About the role**
We are seeking a **Product Security Engineer** to join our multi-functional team and play a critical role in ensuring the security and compliance of our medical device platforms. In this role, you will work closely with Regulatory, Quality, Medical Affairs, R&D, and other key team members to guide secure product development and reduce risk across our product portfolio. You will lead product security risk assessments, support secure architecture and coding practices, and drive the implementation of industry-standard security measures across existing and new products.
Your contributions will be instrumental in maintaining compliance with global regulatory standards (FDA, MDR), enhancing vulnerability management processes, and supporting documentation efforts. You will also be vital in promoting secure software development through collaboration, education, and hands-on technical guidance. We encourage you to apply if you are passionate about product security, regulatory compliance, and making a difference in the healthcare industry.
**Main responsibilities will include:**
+ Work closely with Regulatory, Quality, Medical Affairs, and other teams and support them with security knowledge to improve our product platforms.
+ Alignment with Regulations: Guarantee products align with relevant security standards and regulations.
+ Risk Management: Lead product security risk assessments and implement effective mitigation strategies.
+ Support & Collaboration: Partner with multi-functional teams to resolve vulnerabilities in current products and uphold continuous security compliance.
+ Support teams in reducing product risk by finding practical solutions on how to increase security in new and existing products
+ Work in a team supporting R&D in implementing secure software solutions by ensuring the architecture follows industry-accepted standards for medical device security, including encryption, disaster recovery, authentication, audit logging, hardening measures, patch management, and vulnerability monitoring.
+ Assist in product security risk assessments and provide vulnerability remediation guidance to product development software engineers, both on and off-site.
+ Develop and ensure that software engineering procedures are aligned with product security requirements
+ Supporting the Product Security Documentation process, including:
+ Providing standardised Product Security documentation
+ Organise and support the document review and approval process
+ Ensure that work is completed punctually and to the required level of quality
+ Interface and oversee product security aspects of technical departments such as Systems Hardware, Quality, and technical services
+ Collaborate with other BD resources to ensure effective design and implementation goals.
+ Assure alignment to BD development policies and software quality procedures.
**About you**
+ BS degree in Computer Science, Computer Engineering, Electrical Engineering, or other related engineering field or equivalent work experience required
+ Experience in IT-Security, Cybersecurity, secure software development and designs, and risk management. Solid understanding of current regulatory Compliance & Standards
+ Working experience with various encryption algorithms and PKI solutions
+ Experience in creating documentation for software products
+ High level of self-organisation and delivering required inputs on time
+ Experience with Dynamic and static code analysis tools
+ Knowledge of completing a track, Trace and plan using a Security Requirements Traceability Matrix (SRTM) or similar tool with the goal of tracking
+ Security Requirements, Source of Requirement, Requirement Objective and Verification Method experience
+ Understanding of vulnerability scans and static code analysis results
+ Understanding proper secure coding practices to drive standards within the software engineering organisation
+ Experience working in a regulated environment
+ Basic understanding of network security fundamentals (IP protocol, firewalls etc.)
+ Recognised Security certifications are a plus (CISSP, CASP+, CSSLP, etc)
+ Understanding of security issues and solutions for embedded devices
+ Good understanding of networking and related security aspects, and common attacks
+ Demonstrated knowledge of developing in a regulated environment and adhering to a quality management system
+ Excellent written and verbal communication and interpersonal skills are critical
+ Demonstrated positive work ethic with a strong commitment to achieving project goals
+ Good understanding of Microsoft Office products and tools
**Click on apply if this sounds like you!**
Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to 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, and other legally-protected characteristics.
**To learn more about BD visit:** ** Skills
Optional Skills
.
**Primary Work Location**
IRL Limerick - Castletroy
**Additional Locations**
**Work Shift**
At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You ( .
Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed.
The salary or hourly rate offered to a successful candidate is determined by their experience, education, and skills, as well as the labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location.
**Salary Range Information**
43,300.00 - 73,600.00 EUR Annual
Becton, Dickinson and Company 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.

Job Description Summary This position is for a Security Engineering role within BD's Product Security Organisation. The future candidate would be responsible for/supporting the Inffusion OUS portfolio, including projects like BD neXus and the BD Infusion legacy portfolio. The candidate should be strong in software documentation and technical security aspects. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. Why join us? A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place. Become a maker of possible with us! Our vision for Medication Management Solutions at BD With our technical capabilities, the Medication Management Solutions (MMS) team are able to manage multiple systems and our operational capabilities enable us to have medications available when and where needed, reducing inefficiency and waste for nursing and pharmacy teams. About the role We are seeking a Product Security Engineer to join our multi-functional team and play a critical role in ensuring the security and compliance of our medical device platforms. In this role, you will work closely with Regulatory, Quality, Medical Affairs, R&D, and other key team members to guide secure product development and reduce risk across our product portfolio. You will lead product security risk assessments, support secure architecture and coding practices, and drive the implementation of industry-standard security measures across existing and new products. Your contributions will be instrumental in maintaining compliance with global regulatory standards (FDA, MDR), enhancing vulnerability management processes, and supporting documentation efforts. You will also be vital in promoting secure software development through collaboration, education, and hands-on technical guidance. We encourage you to apply if you are passionate about product security, regulatory compliance, and making a difference in the healthcare industry. Main responsibilities will include: Work closely with Regulatory, Quality, Medical Affairs, and other teams and support them with security knowledge to improve our product platforms. Alignment with Regulations: Guarantee products align with relevant security standards and regulations. Risk Management: Lead product security risk assessments and implement effective mitigation strategies. Support & Collaboration: Partner with multi-functional teams to resolve vulnerabilities in current products and uphold continuous security compliance. Support teams in reducing product risk by finding practical solutions on how to increase security in new and existing products Work in a team supporting R&D in implementing secure software solutions by ensuring the architecture follows industry-accepted standards for medical device security, including encryption, disaster recovery, authentication, audit logging, hardening measures, patch management, and vulnerability monitoring. Assist in product security risk assessments and provide vulnerability remediation guidance to product development software engineers, both on and off-site. Develop and ensure that software engineering procedures are aligned with product security requirements Supporting the Product Security Documentation process, including: Providing standardised Product Security documentation Organise and support the document review and approval process Ensure that work is completed punctually and to the required level of quality Interface and oversee product security aspects of technical departments such as Systems Hardware, Quality, and technical services Collaborate with other BD resources to ensure effective design and implementation goals. Assure alignment to BD development policies and software quality procedures. About you BS degree in Computer Science, Computer Engineering, Electrical Engineering, or other related engineering field or equivalent work experience required Experience in IT-Security, Cybersecurity, secure software development and designs, and risk management. Solid understanding of current regulatory Compliance & Standards Working experience with various encryption algorithms and PKI solutions Experience in creating documentation for software products High level of self-organisation and delivering required inputs on time Experience with Dynamic and static code analysis tools Knowledge of completing a track, Trace and plan using a Security Requirements Traceability Matrix (SRTM) or similar tool with the goal of tracking Security Requirements, Source of Requirement, Requirement Objective and Verification Method experience Understanding of vulnerability scans and static code analysis results Understanding proper secure coding practices to drive standards within the software engineering organisation Experience working in a regulated environment Basic understanding of network security fundamentals (IP protocol, firewalls etc.) Recognised Security certifications are a plus (CISSP, CASP+, CSSLP, etc) Understanding of security issues and solutions for embedded devices Good understanding of networking and related security aspects, and common attacks Demonstrated knowledge of developing in a regulated environment and adhering to a quality management system Excellent written and verbal communication and interpersonal skills are critical Demonstrated positive work ethic with a strong commitment to achieving project goals Good understanding of Microsoft Office products and tools Click on apply if this sounds like you! Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to 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, and other legally-protected characteristics.

Mechanical Design Engineer Location: Dublin (Hybrid) Salary: €4000- €5000 An expanding international M&E consultancy is seeking a Mechanical Design Engineer to lead and deliver innovative design solutions across a range of projects. Responsibilities: Lead and manage mechanical engineering project teams from concept to completion. Oversee project design, coordination, cost management, and profit delivery. Support Directors with business strategy, sector growth, and office management. Maintain strong client relationships and actively contribute to business development. Manage tender and procurement of MEP contractors and equipment Provide technical leadership in design, calculations, controls, and operating systems. Contribute to risk management, internal controls, and project reporting. Requirements: Degree (BSc/BEng) in Mechanical/Building Services Engineering or equivalent. Significant experience delivering mechanical design for diverse building types. Strong knowledge of Irish building regulations, BS/EN standards, and health & safety. Skilled in MS Office and engineering calculation software. Excellent presentation, communication, and client-facing skills. Ethical conduct and commitment to professional standards. Benefits: 23 days annual leave, rising to 28 after 5 years. Salary: 00- 000 Hybrid working model. Contributory pension scheme. Company healthcare scheme. Non-contractual bonuses. Training sponsorship and career development. Interested? Email or call for a confidential chat. Skills: Mechanical Design Engineer

If you are aMechanical Design Engineerwho is looking for your next career move, please send your CV toGrace Birchor callfor a confidential discussion. Duties: Assist in the development of mechanical designs, drawings, and 3D models under guidance to meet project requirements and standards. Collaborate with team members to support the integration of mechanical systems into project designs. Perform basic calculations and support simulations to help optimize system performance and efficiency. Contribute to the preparation and review of technical documentation to ensure alignment with codes and standards. Participate in design reviews, risk assessments, and site inspections to learn and contribute to quality and safety outcomes. Requirements: Hold a degree in Mechanical Engineering. Must have 3+ years of experience as a Mechanical Design Engineer with an Irish consultancy (local knowledge essential for the role). Demonstrate excellent communication skills. Proficiency in AutoCAD is required, and experience with Revit is a plus. Salary & Benefits: €45K to €60K DOE 24 annual leave days a year Annual Bonus Health Insurance If you are aMechanical Design Engineerwho is looking for your next career move, please send your CV toGrace Birchor callfor a confidential discussion. Skills: Mechanical Design Engineer

Opportunity to join leading global industrial and automotive electronics component organisation in their city center office. Reporting to the Mech. Design Lead, involved in producing 3D models, 2D drawings and documented work instructions according to Design Standards using SolidWorks. Knowledge of 3D printing and FEA an advantage To be accurate and consistent in the production of work instructions and drawings. Must be able to work in a team environment. Work with design engineers in other manufacturing locations to release new products. Cooperate with engineering teams in customers during custom design projects. To positively contribute towards the continuous improvement philosophies, in work and work-related activities. Degree in Mechanical Engineering or equivalent. 1-5 years mechanical design experience ideally for a similar product range. Demonstrated knowledge and experience in SolidWorks. Good planning and organisational skills and ability to prioritise. Deadline and detail oriented. Benefits: Group Life Assurance Medical Aid / Health Care Paid Holidays Pension Fund