Senior Engineer, Process Development, Advanced Operations page is loaded## Senior Engineer, Process Development, Advanced Operationslocations: Cork, Irelandtime type: Full timeposted on: Posted Todayjob requisition id: R551882Work Flexibility: Onsite**Permanent hybrid role based in Carrigtwohill, Cork****Position Summary:*** Independently determines and develops approaches to a variety of technical problems of moderate scope and complexity.* Uses latest engineering techniques to reduce product time to market whilst adhering to regulatory requirements, project deadlines and product costs.* Builds productive internal and external working relationships and may periodically provide guidance and train other team members.**Key Areas of Responsibility:*** Process development and characterisation of machining & manufacturing processes for R&D / NPD on multi-axis CNC machines. Create production programs (G code / CADCAM), conduct experimental tests and analyse results to establish optimum process operating parameters. Lead and/or participate in process review meetings.* Work with tooling suppliers to identify and optimise tooling and fixturing for CNC manufacturing processes. May lead/support capital acquisition activity from specifying equipment, testing, liaising with equipment / component suppliers.* Input into process technology road-mapping activities and drive innovation to ensure alignment with future planned product launches.* Work with quality & metrology engineers to develop component specific testing and inspection protocols. Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product launches.* Complete capability studies for process control and generate subsequent production documentation ensuring that all activities are completed and documented in accordance with Stryker new product development procedures.* Complete process qualification (IQ/OQ/PQ) of multi axis CNC manufacturing processes and any other processes as required by the project. Review and approval of validation documentation.* Provide engineering support for new product and process introductions. Provide training to manufacturing team members and other Engineers.* Ensure adherence to GMP and safety procedures.* All other duties as assigned.## Qualifications Knowledge Skills:* B.S in Mechanical / Manufacturing / Precision Engineering or related engineering discipline with 2 or more years’ industry experience.* **Passion for CNC machining** and **high precision manufacturing processes**. Hands-on machining experience with multi-axis CNC machining (**grinding** / mill-turn / sliding head etc. ) would be advantageous.* Knowledge of CAD/CAM and CNC coding would be advantageous.* Must be able to read and interpret complex engineering drawings and have the ability to understand geometrical dimensioning and tolerancing.* Excellent interpersonal skills – must be able to express ideas to the wider cross functional team, collaborate with cross functional teams to achieve project goals, and be open minded with the ability to recognise good ideas.* Innovative thinker - should be able to envisage new and better ways of doing things. Continuous improvement and lean 6 sigma mindset advantageous.* Experience in executing complex problem solving techniques related to manufacturing/design technical issues. Good instincts and sound judgement for mechanical and structural design.* Excellent analytical skills, ability to accurately plan, organise and implement concurrent tasks.* Good knowledge of manufacturing processes, inspection equipment, materials and process design.* Experience in an FDA regulated or regulated industry beneficial.* Excellent attention to detail.Travel Percentage: 10% #J-18808-Ljbffr
A leading medical device company in Cork is seeking a Quality Engineer to work within the quality operations team. This role involves ensuring quality performance of products and processes, supporting manufacturing transfers, and maintaining quality KPIs. A Bachelor of Science or Engineering is required, along with 0-2 years of industry experience. This is a hybrid position with a contract of 18 months and full company benefits. #J-18808-Ljbffr
Principal Engineer, R&D page is loaded## Principal Engineer, R&Dlocations: Cork, Irelandtime type: Full timeposted on: Posted Todayjob requisition id: R557402Work Flexibility: Hybrid**Who we want:**We are seeking an R&D Engineer who is passionate about innovation and motivated by solving complex clinical challenges to help develop our next generation of neurosurgical products in the cranial space. This role offers a unique opportunity to work at the intersection of advanced engineering and life-saving medical technology.The ideal candidate is driven by the desire to make a meaningful difference in patients’ lives and is energized by translating engineering principles into safe, effective, and intuitive solutions for surgeons. You will contribute to the design and development of cutting-edge technologies, working closely with cross-functional teams including clinicians, researchers, and manufacturing partners.Through creativity, technical rigor, and a strong sense of purpose, you will help push the boundaries of what is possible in neurosurgery—delivering innovations that directly improve patient outcomes and quality of life.**What you will do:**Technical Responsibilities:• Lead technical team members in research, design, development, modification and evaluation of modules, assemblies, or subsystems • Apply advanced engineering theories, principles, and concepts across various products within business • Translate user needs to design inputs/ specifications and produce system/architectural level layouts and platform designs • Assess new technologies and capabilities (prototyping, testing, et.al.) for the organization • Mentor and influence in correction of complex product design issues • Navigate the Intellectual landscape for filings and protection Business Responsibilities: • Possess an in-depth knowledge of the industry and competitive landscape • Partner with customers, internal and external key opinion leaders to develop technical strategies that meet clinical needs • Strategize and execute customer facing activities like voice of customer and customer centric design across the business • Collaborate on Financial /business modeling and supports business reviews to validate a technical approach Med Device Compliance: • Divisional expert with extensive experience applying industry standards for device development • Independent reviewer and advisor for the creation or refinement of engineering documentation, such as the Design History file • Lead the development of standards and regulations, working closely with functions within and across business General Responsibilities: • Lead cooperative efforts with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success • Lead and support team members to create or improve procedures, policies, processes, systems, and technology requirements • Develop and utilize tools to enhance the company’s product/process development or performance • Identify and implement design and process solutions and ensures they are sustained over time • Lead and support complex product development for cross functional teams, influencing multiple technical areas of expertise • Hold team accountable to deliver high quality results with passion, energy and drive to meet business priorities • Mentor, develop and influence across the business, intentionally building divisional relationships **Minimum Qualifications (Required):** • Bachelor of Science in Engineering, Mechanical Engineering, BioMedical Engineering or similar & 8+ years of work experience **Preferred Qualifications (Strongly desired):** Technical Skills: • Broad base of experience in Implementing design methodologies such as DFM, Reliability, Systems Design • High degree of experience in medical device design (or designing in a highly regulated industry) and ability to utilize Solid Modeling and CAE tools to optimize the design • In-depth knowledge of materials, manufacturing and processing methods and technologies to support complex product development • Ability to communicate complex plans and technical information to team members within and across businessesTravel Percentage: 20% #J-18808-Ljbffr
A leading medical technology company in Cork, Ireland, is seeking a Principal Engineer, R&D to innovate and develop neurosurgical products. The role requires a passion for solving clinical challenges and transforming engineering principles into effective solutions. The ideal candidate will lead technical teams, ensure compliance with industry standards, and collaborate across business units to improve patient outcomes. A Bachelor’s degree in engineering with over 8 years of experience is required. This position supports a hybrid work model. #J-18808-Ljbffr
Quality Engineer page is loaded## Quality Engineerlocations: Cork, Irelandtime type: Full timeposted on: Posted Yesterdayjob requisition id: R556325Work Flexibility: Hybrid or OnsiteThis is an 18 month contract with full Stryker benefits.This is a Hybrid role with 2 days a week from home.**What you will do:** Will work within the quality operations team, with moderate supervision and mentoring, with responsibility for quality related activities, including, but not limited to the following:* Work closely with operations and the business functions to ensure quality performance of product and processes.* Approval of NC, builds proficient in problem solving and root causing activities.* Participate in the development and improvement of the manufacturing processes for existing and new products.* Review of change management activities.* Maintain KPIs for monitoring of process quality, perform analysis and interpret trends, take action as necessary.* Support execution and analysis of QATs.* Advocate of Human Factor practices, familiarity in the science of Human Factor identification, reduction and mitigation.* Develop understanding of risk management practices and concepts, ability to become proficiency in process risk.* Develop understanding of optimization of inspection methods and sampling. Support First Article Inspections.* Developing proficiency in statistical methods and application.* Participate and interface in internal audits providing effective narrative and description of topic of expertise, participate in external audits preparation building confidence and proficiency in interactions with same.* Assist in the development and review of process and equipment validation/qualification. Build proficiency in validation processes.* Support manufacturing transfers to other plants/facilities, execution quality activities.* Responsible for initiation, internal containment and support of ship and product holds for potential product escapes. **What you will need:*** Masters or Bachelor of Science, Engineering or related subject- Level 8 Degree* 0-2 years experience in industry desirable Travel Percentage: 0% #J-18808-Ljbffr
A global medical technology company in Carrigtwohill is seeking a Senior Staff Engineer, Mechanical Design to lead the development of electro-mechanical devices. You will work closely with a dedicated R&D team to innovate surgical solutions while managing project timelines and mentoring engineers. The ideal candidate has over 6 years of engineering experience, particularly in mechanical design and DFM principles, with a strong background in creating complex systems. This hybrid position offers a unique opportunity to impact patient care and surgical outcomes. #J-18808-Ljbffr
Senior Project Engineer page is loaded## Senior Project Engineerlocations: Carrigtwohill, Irelandtime type: Full timeposted on: Posted Todayjob requisition id: R550166Work Flexibility: Hybrid or Onsite**Position Summary:**In this role, you will design and develop solutions for Orthopaedic and Trauma applications, while leading technical execution across cross-functional teams through the new product development process. You’ll also provide oversight on adjacent project efforts and take ownership of technical aspects across the broader program pipeline. **What you will do:*** Independently design and implement complex concepts and systems including system architectural design, relevant design documentation, test planning and execution* Specialize in various technology domains and evaluates new technologies* Support designs and the selection of platform technologies* Work independently with surgeon customers in a user setting, clearly communicate design goals and incorporate feedback into designs* Ensure compliance with the relevant requirements in cooperation with other engineering disciplines, QA/RA/AO, etc.* Maintain and improve engineering methods and practices* Train and mentor regarding established engineering best practices, design principles, processes and tools* Work with core team to determine project schedules and time commitments of self and other functional project team members and be able to clearly communicate status of assignments to project management.* Perform holistic problem analysis* Design and implement solutions to address identified problems* Support the implementation of state-of-the-art technologies**What you will need:*** Bachelor's degree in science, prefer Mechanical or Biomedical Engineering, prefer Masters Degree in a technical discipline* Minimum of 2 years industry experience* Product design experience in Orthopaedics in the medical device industry or related Engineering/Manufacturing industry experience* Demonstrated leadership of technical work groups* Experience in the function, clinical issues and performance requirements of Orthopaedic implants* Experience leading complex product development initiatives from concept through release* Experience in design controls and risk management within a regulated industry* Experience with a parametric CAD design package. Prefer ProE* Demonstrated understanding of Finite Element Analysis (FEA) and its application#IJTravel Percentage: 20% #J-18808-Ljbffr
A leading medical device company in Carrigtwohill, Ireland is seeking a Senior Project Engineer to design and develop Orthopaedic and Trauma applications. The role involves leading cross-functional teams, ensuring compliance with engineering requirements, and mentoring others in established practices. Candidates should have a Bachelor's degree in Mechanical or Biomedical Engineering, with a minimum of 2 years of industry experience and expertise in product design and leadership. Hybrid or onsite work flexibility is offered. #J-18808-Ljbffr
Senior Staff Engineer, Mechanical Design - R&D page is loaded## Senior Staff Engineer, Mechanical Design - R&Dlocations: Carrigtwohill, Irelandtime type: Full timeposted on: Posted Todayjob requisition id: R556681Work Flexibility: Hybrid or OnsiteStryker presents an exciting opportunity to join a highly motivated R&D team in developing key technology to enable the evolution of new surgical techniques in electrosurgery. The successful candidate will work with a multi-disciplined team at our Innovation Centre in Cork and focus on establishing the needs of our customers while designing and bringing innovative solutions for electrosurgery applications to market.The Innovation Centre, which features unique design and collaboration workspaces, state-of-the-art prototyping and test facilities, and a simulated operating room, is the first of its kind in Ireland. The centre focuses on the development of new technologies and products to improve patient safety and outcomes during surgery, and increase operating room efficiency across multiple surgical specialties including neuro, spine, ENT and orthopaedic surgery.The successful candidate will design, develop, refine and evaluate electro-mechanical components, assemblies or subsystems for electro-mechanical medical devices. You will use concurrent engineering and rapid prototyping techniques to reduce product time to market whilst adhering to project deadlines and product costs. You will plan and execute successful product development projects, occasionally leading and training team members on technical aspects of product commercialization.**What you will do:** Technical Responsibilities: • Lead research, design, development, modification and evaluation of modules, assemblies, or subsystems • Apply and mentor others on advanced engineering theories, principles, and concepts • Translate user needs to design inputs/ specifications and produce complex system level designs independently • Conduct, design, and select advanced prototyping and testing • Lead and guide in correction of complex product design issues • Conduct technology exploration and influence application in the business • Develop invention disclosures, patents or trade secrets Business Responsibilities: • Contribute to competitive and market strategy by demonstrating in-depth knowledge of the market, customer dynamics and competitive offerings • Apply strong understanding of clinical procedures to enhance product development • Contribute and execute customer facing activities like voice of customer and customer centric design in partnership with internal and external stakeholders • Demonstrate financial acumen Med Device Compliance: • Mentor others as a business unit expert on the usage of industry standards, including design requirements and test strategies per applicable regulations • Lead others to create and refine engineering documentation, such as the Design History file and create more progressive technical content • Contribute to R&D procedures and development of industry standards working closely with cross-functional business units General Responsibilities: • Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success • Identify and lead the creation of or improvements to procedures, policies, processes, systems, and technology required • Develop, Research, Prototype, leveraging multiple methodologies for evaluation • Contribute to complex product development through release and lead one technical area of expertise • Hold self and others accountable to deliver high quality results with passion, energy and drive to meet business priorities • Mentor, develop and inspire others in current and future roles • Collaborate and influence others on cross functional teams advancing partnerships to achieve business objectives **Minimum Qualifications (Required):** • Bachelor of Science in Engineering, Mechanical Engineering or BioMedical & 6+ years of work experience **Preferred Qualifications (Strongly desired):** Technical Skills: • Experience in developing and optimizing complex designs for mechanical / electro-mechanical assemblies incorporating DFM principles • Experience in creating engineering drawings, models, applying GD&T and CAE tools to optimize the design • In-depth knowledge of materials, manufacturing and processing methods and technologies to support complex product development • Ability to communicate complex plans and technical information to team membersTravel Percentage: 20% #J-18808-Ljbffr
Senior Packaging Engineer page is loaded## Senior Packaging Engineerlocations: Cork, Irelandtime type: Full timeposted on: Posted Todayjob requisition id: R550924Work Flexibility: HybridSenior Packaging Engineer (12 months FTC - Maternity cover)## Position SummaryThe Senior Packaging Engineer, R&D Packaging will be a member on new product development and sustaining project teams with responsibilities for development of packaging components, artwork design, design verification, shelf life testing and compliance related activities. This resource will also lead teams on special activities and research which have business impact. ## ## What you will do* Execute packaging usability research and participate in Voice of the Customer activities.* Develop packaging components that improve the customer experience, working with a drafter to develop 3D models and Artwork.* Demonstrate development life cycle knowledge through delivery of high quality deliverables.* Work cooperatively with quality, manufacturing, regulatory, clinical, marketing, R&D device designers, supply chain, vendors, and distribution centers – across geographies -- to ensure project success.* Build Quality into all aspects of product development and support by maintaining compliance to all quality requirements and leading improvements and development of solutions that make it easier for the organization to maintain compliance in complex areas (such as ever-evolving regulatory requirements worldwide).* Support audits, non-conformances and CAPAs as needed.* Lead small- scale Packaging projects to drive changes across the packaging team.* Mentor or supervise technical staff as needed.* Role-model a high level of service and responsibility in managing a high and varied workload from internal clients and working to tight timelines.## What you will need* B.S. degree in Packaging, Industrial, Mechanical engineering or applicable technical field.* 2+ years of experience* Medical device industry experience preferred* Demonstrated experience in medical device, biotech or pharmaceutical packaging design development.* Demonstrated experience in resolving design and process related packaging issues on commercial products* Functional knowledge of Design Controls and Industry standards in Packaging Design (11607, ASTM, ISTA)* Experienced in Statistical Analysis, interpretation and communication of results* Excellent interpersonal and communication skills* Strong technical capabilities and project management capability to develop aspects of assigned projects on time and within budget.#IJTravel Percentage: 10% #J-18808-Ljbffr
