## Manager, EngineeringApplylocations: Cork, Irelandtime type: Full timeposted on: Posted 2 Days Agojob requisition id: R563729Work Flexibility: Hybrid or Onsite## Position SummaryThe Manufacturing Engineering Manager leads a manufacturing engineering team responsible for sustaining, improving and scaling robust manufacturing processes for neurovascular products in a regulated medtech environment. The role is accountable for process capability, product quality, capacity, cost and service performance across the manufacturing value stream, while ensuring compliance with site quality systems, EU MDR, ISO 13485 and, where applicable, FDA 21 CFR Part 820 / QMSR requirements. Working cross-functionally with Operations, Quality, R&D / Process Development, Supply Chain, EHS and external partners, the role drives NPI transfer, validation, automation, capital deployment and continuous improvement to support safe, compliant and efficient manufacturing.## What you will do* Responsible for assigned Manufacturing Engineering teams, including performance management, prioritisation of resource assignments, recruitment, mentoring and supervision.* Champion effective employee relations and communication within the department, while demonstrating a flexible management style, utilizing the appropriate style for the given situation.* Create a highly talented Value Stream team and champion a positive employee environment by promoting open communication, engagement and development of team members. Promote a culture of inclusiveness, trust, cooperation and a commitment to teamwork.* Select and develop a talented and competent team of Engineering Professionals. Coach and mentor employees, and support continuous learning and development toward a performance excellence goal.* Develop SMEs (subject matter experts) as necessary to both foster initiatives in strategic areas, and to provide follow-on support to manufacturing in respect of completed projects in such areas.* Agree and drive operational excellence by setting clear direction and expectations for performance. Establish performance targets for the Value Stream, and measure actual performance with respect to Product Quality, Customer Service, department spending, labour efficiency and yield against targets. Takes appropriate and timely corrective action if negative trends begin to emerge.* Provide leadership and direction to team on process improvements, address obstacles, provide resources and interact with other areas of the company to assist team in overcoming problems and streamlining the work process as part of a structured continuous improvement program.* Works proactively with business management peers and site leadership to deliver business objectives – lean manufacturing metrics, cycle time, efficiency, space utilisation, scrap as %VOP etc.* Development of a world class-manufacturing group that is proficient in process improvement and problem solving manufacturing issues using Six-Sigma tools.* Driving IBP (Integrated Business Plan) contract deliverables by providing input on process technology selection.* Collaborate with R&D partners to ensure that all new products and processes are introduced into production in compliance, on time, within budget and are operationally successful.* Development of, and management of spend against departmental budgets and capital spending approvals.* Lead and/or represents the function in periodic business metric reviews.* Initiates cross-functional partnerships to identify and resolve production / engineering issues.* Ensures provision of out-of-hours support to the business as required or mandated by shutdowns, projects, quality issues and/or equipment failures.* Actively interfaces all other business functions, 3rd part Vendors / Suppliers, and sister sites, and always practices good team work in support of the day to day operating requirements in pursuit of achieving the business targets* Develops and maintain relationships with technical management in sister sites and R&D* Fostering a work environment of continuous improvement that supports SYK’s Quality Policy, Quality System, and the appropriate regulations for the area they support, in particular ensuring that employees are trained to do their work and their training is documented.* Observing the Quality Management Systems requirements on site at all times* Keeps oneself abreast of all relevant technological advancements and oversees the specification and purchase of capital equipment, ensuring a balance between optimizing technological capabilities and return on investment.* Manages the planning and execution of process and equipment validations per SYK NV requirements.## What you will need* Degree or Masters in relevant Engineering or Science discipline (Manufacturing, Mechanical, Electronic, Production etc.), with a minimum of 10 years relevant experience in a team based regulated manufacturing environment, and ideally 5+ years’ experience at a senior / management level.* Good knowledge of GMP / FDA regulatory requirements and current Health and Safety Regulations legislation.* Proven track record delivering manufacturing performance improvements in areas such as yield, scrap, cycle time, quality, capacity and cost.* Strong analytical, problem-solving and stakeholder-management capability; Lean / Six Sigma experience preferred.* Strong leadership skills, a confident and effective decision maker, with a proven leadership ability to negotiate and influence others.* Excellent presentation and written / verbal communication skills* A team player, with a flexible approach.* Clearly demonstrable ability to work autonomously* Technological pioneer, willing to source, investigate and implement technological and automation advances on the floor* There may be a requirement as part of the role to travel to other sites #J-18808-Ljbffr
Prototype Technician, Engineering Services page is loaded## Prototype Technician, Engineering Serviceslocations: Cork, Irelandtime type: Full timeposted on: Posted Todayjob requisition id: R565201Work Flexibility: Onsite**Prototype Technician****Permanent role**Builds prototype medical device products and components using automated, semi-automated and manual methods. With minimal input can determine which processes should be used for fastest manufacture of prototypes. Gives feedback and input to design and manufacturing engineers on prototyping capability as it applies to component tolerancing and features.**What you will do:*** Support R&D and AO during new product introductions including input into product and process design reviews, fixture/tooling design and design for manufacturing.* Design complex prototypes and fixtures by use of CAD/CAM. Build fixtures and related apparatus as needed for assigned project.* Work from engineering schematics and/or specifications and use precision measuring equipment to ensure components and finished products meet design specifications and highest engineering and quality standards.* Specify, evaluate and order new equipment, tooling, materials and supplies as required for each new assignment.* Comply with all new product documentation and process control.* Train and/or assist others in product development and design for related topics.* Work closely with external toolrooms and suppliers to outsource work and resolve technical challenges.* Will be required to comply with documentation procedures and maintain experimental laboratory housekeeping standards to the highest level.* Will coordinate with facilities and assist in the maintenance of prototype equipment, fixtures and fittings.* Provides guidance on prototype manufacturing methods.**What you will need**:* Tool Making or similar craft qualification or a Certificate in an Engineering discipline with related work experience in a precision machining environment.* Experience in machining a wide variety of metals, and plastics.* Demonstrated ability to program and operate CNC and manual machine tools, small hand tools, power tools and test/inspection equipment.* Must be able to analyze and resolve complex machining issues of a broad scope using independent judgment.* Must have the ability to quickly master the operation of new equipment, machine tools, software packages and programming languages using own initiative.* Ability to read and understand complex engineering drawings.* Excellent attention to detail - must be able to observe and correct minute inconsistencies (e.g. in engineering drawings, printed word, product appearance, etc.)* Must be able to follow detailed instruction and inspection procedures. Must be able to complete detailed documentation accurately.* Must have ability to manage multiple project requests simultaneously.* Advanced maths and measuring skills.* Excellent problem solving skills.Travel Percentage: None #J-18808-Ljbffr
Stryker Corporation is looking for an Associate Manager, Workplace Operations to oversee its Innovation Centre in Cork, Ireland. This role encompasses the management of daily operations, vendor performance, and compliance with regulatory standards. The ideal candidate will bring over 6 years of facilities management experience, strong organizational skills, and proficiency in building management systems. Responsibilities include team management, maintenance oversight, budgeting, and project coordination. This role supports a dynamic environment promoting innovation and collaboration. #J-18808-Ljbffr
Stryker Corporation in Cork, Ireland is seeking a Lead Systems Engineer for a permanent position within the Additive Institute. The role involves researching and developing medical device systems while leading integration testing and system verification. Candidates should possess a Bachelor of Science degree in Engineering and have at least four years of related experience. Strong technical skills in requirements management and system modeling are preferred. This role offers a hybrid working model and requires collaboration with cross-functional teams. #J-18808-Ljbffr
## Staff Engineer, Systems EngineeringApplylocations: Cork, Irelandtime type: Full timeposted on: Posted 2 Days Agojob requisition id: R564747Work Flexibility: Hybrid**Lead Systems Engineer****Role:** Permanent**Location:** Stryker Anngrove, our state of the art Additive InstituteVery flexible hybrid working model.**What you will do:** **Technical Responsibilities:** • Independently research, design, develop, modify, and verify medical device systems • Translate user needs to system requirements • Modify existing system architectures or test designs • Create new system architectures or test designs for simple product or features • Allocate and decompose requirements on a multi-disciplinary (electrical, mechanical, software) project using modeling, simulation, budgeting, or mathematical techniques • Lead Concept Phase activities for a feature • Analyze and correct complex product design issues using independent judgment • Lead analytical studies, including trade studies, sensitivity studies, optimization studies, performance assessments, and design assessments • Lead system integration testing and verification activities • Contribute to Product Risk Management activities **Business Responsibilities:** • Advance solutions by applying in-depth knowledge of customer needs, market, and competitive offerings • Apply detailed knowledge of clinical procedures to author design inputs • Support Voice of Customer sessions internally and with clinicians • Demonstrate developing financial acumen Med Device Compliance: • Be proficient with and mentor others in usage of industry standards, including design requirements and test strategies per applicable regulations • Lead creation and refinement of engineering documentation, such as the Design History file • Follow and mentor others on R&D procedures like design controls and risk management, per the Quality Management System **General Responsibilities:** • Work cooperatively with all stakeholders to ensure project success • Identify and support the creation of or improvements to procedures, policies, processes, systems, and technology • Support and execute segments of complex multifunctional teams to advance projects through the design /development/launch process • Deliver high quality results with passion, energy, and drive to meet business priorities • Collaborate with cross-functional teams to build partnership to achieve business objectives **Minimum Qualifications (Required):** • Bachelor of Science in Software, Electrical, Mechanical, Systems, or Biomedical Engineering & 4+ years of work experience **Preferred Qualifications (Strongly desired):** **Technical Skills:** • Strong technical ability to develop and optimize system requirements, designs, and verification • Working knowledge of Requirements Management Tools and System Modeling Tools • Ability to communicate moderate complexity plans and technical information to team members **Preferred Skills / Engineering tools:** • Requirements Management Software, especially Jama • Experience with SysML and Model-based Systems Engineering • Experience with SysML / MBSE software tools • Knowledge of ISO 13485 and ISO 14971#IJTravel Percentage: 10% #J-18808-Ljbffr
## Associate Manager, Workplace OperationsApplylocations: Cork, Irelandtime type: Full timeposted on: Posted 2 Days Agojob requisition id: R565048Work Flexibility: Onsite**Associate Manager, Workplace operations - Stryker Innovation Centre Cork**The Associate Manager, Facilities plays a key role in supporting Stryker’s Innovation Centre — a global R&D hub focused on the research and development of advanced medical instrumentation. This position is responsible for overseeing the daily operations, maintenance, and continuous improvement of the facility to ensure a safe, efficient, and high-performing environment that enables innovation and collaboration. The role leads facility operations, vendor management, and maintenance activities while ensuring compliance with regulatory, quality, and safety standards.**What you will do:*** Recruit, train, develop, and manage performance of facilities team members - Set direction, expectations, and priorities for the team to meet operational goals.* Oversee inter-office moves, organizational changes, and resource allocation.* Manage the day-to-day functioning of assigned facilities, including building systems, equipment, and infrastructure* Supervise central services such as security, reception, cleaning, waste disposal, catering, parking, and mailroom function* Coordinate preventive and corrective maintenance, inspections, and repairs.* Maintain building management systems, inventory control, 6S, and housekeeping standards.* Respond promptly to facility and equipment issues, alarms, and system failures.* Plan and oversee facility construction and refurbishment projects, including new equipment installations, in close collaboration with Program and Project Managers* Serve as or direct a construction administrator/project manager to ensure adherence to specifications, schedules, and budgets.* Ensure compliance with relevant regulations, codes, and standards (e.g., health, safety, environmental, quality, ISO, GMP, LEED).* Conduct and document regular facility audits and inspections.* Monitor and promote energy efficiency and environmental sustainability initiatives.* Assist in developing and managing operating and capital expenditure budgets - Track expenses, review contracts, and approve purchases.* Partner with procurement to obtain quotes, negotiate vendor contracts, and optimize cost savings.* Manage vendor performance, ensuring delivery schedules, quality, and service agreements are met.* Prepare reports on facility conditions, operations, and project status.* Maintain records of inventory, repairs, inspections, and compliance documentation.* Liaise with property managers, landlords, and internal stakeholders as needed.* Ensure proper facility coverage and be available or on-call 24/7 to support the business* Actively support the Global RE&F team, collaborating with the wider team to deliver assistance across the UK&I region when required.**What you need:*** Honors Bachelor’s degree in Facilities Management, Engineering, Business Administration, Project Management, or related field; equivalent experience considered.* 6+ years of relevant facilities management experience, including supervisory responsibilities.* Knowledge of facility operations, maintenance practices, construction, health and safety regulations, and environmental standards.* Cross functional workplace expertise with experience across multiple facility related disciplines.* Strong planning, organizational, problem-solving, and decision-making skills.* Excellent communication and interpersonal abilities, with a customer service mindset.* Proficiency in Microsoft Office Suite and building management systems.* Manufacturing or multi-site experience preferred#IJ #J-18808-Ljbffr
**This is a 12 month onsite role in Limerick with full Stryker benefits.**Previous industry experience desired. Experience in interacting with regulatory agencies (FDA, MoH, TUV, etc.) desired. Familiarity with ISO 13485, GDP, GMP desired. Strong knowledge of Quality Concepts (e.g. Risk Management, CAPA, Audits, Statistics). Must possess strong communication, project management and influencing skills as well as have the ability to manage multiple tasks simultaneously.Ability to represent Quality function with project teams.Strong interpersonal skills, written, oral communication and negotiations skills. Highly developed problem-solving skills. Strong analytical skills.Demonstrated ability to work independently and as part of cross-functional teams. Experience in working in a compliance risk situation. Support and Drive Human Factor practices, familiarity in the science of Human Factor identification, reduction, and mitigation. Develop understanding of risk management practices and concepts and applies knowledge to manufacturing operations. * Level 8 Degree in Science or Engineering* 2 years experience in Quality #J-18808-Ljbffr
Stryker Corporation is seeking a qualified professional for a 12-month onsite role in Limerick. The ideal candidate will have a Level 8 Degree in Science or Engineering, with at least 2 years of experience in Quality. Candidates should have strong knowledge of Quality Concepts, including ISO 13485 and GMP. Strong communication and project management skills are essential, as well as the ability to work independently and within cross-functional teams. The role involves interacting with regulatory agencies, managing tasks, and supporting Human Factor practices. #J-18808-Ljbffr
Manufacturing Operator (Limerick) page is loaded## Manufacturing Operator (Limerick)locations: Limerick, Irelandtime type: Full timeposted on: Posted Todayjob requisition id: R565178Work Flexibility: OnsiteJob Description**Who we want*** **Performance**: Deliver high quality products.* **Team Player**: Build positive relationships with others to achieve common goals.* **Reliable**: Manage time to effectively get the job done.A Manufacturing Operator at Stryker performs the activities associated with the specific Standard Operation Procedures (SOPs) for the purpose of manufacturing, inspection or packaging of Medical Devices**What you will do**The Manufacturing Operator will be responsible for some or all of the below:* Producing and/or packaging and labeling high quality product within a team environment, in line with standard operating procedures.* Inspecting components by using precision measuring equipment to ensure components meet engineering specifications.* Completing production records and maintenance logs.* Maintaining a high standard of housekeeping* Adhering to all Health and Safety procedures and requirements.* Final Inspection Activities to include finished goods inspection and DHR review.* Demonstrating safe working practices, correct use of equipment, product verification and the adherence to EHS, line clearance and 5 pillars compliance.**What you need*** Leaving Certificate, Trade or equivalent education level is required.* Experience in a regulated manufacturing environment is an advantage* Capable of working as part of a multi-disciplined team* Good Communication Skills* Experience in GMP environment is preferred but not essential**\* This role is initially a 12 month fixed term contract. Please also note that this role is for weekend nights for our Limerick site.**#IJTravel Percentage: None #J-18808-Ljbffr
Senior Staff Data Scientist - Neurotechnology page is loaded## Senior Staff Data Scientist - Neurotechnologylocations: Cork, Irelandtime type: Full timeposted on: Posted Todayjob requisition id: R563955Work Flexibility: Hybrid**This is a hybrid, 18 month fixed term maternity leave contract role based in Carrigtwohill, Cork.****This role does not meet the criteria to allow Stryker to sponsor a Critical Skills work permit. Candidates must be resident in the Republic of Ireland and eligible to work for the full duration of the contract**You will work closely with technical and business leads representing a diverse and robust array of surgical instrumentation, including imaging, visualization, navigation, robotics, and various powered smart instrumentation. You will partner closely with a global R&D team, multi-disciplined OR clinical teams and marketing as we collectively advance neurosurgery and transform the lives of patients. You will: • Provide hands on data engineering to extract valuable insights from Stryker’s connected Neurotechnology ecosystem, enabling data informed clinical performance, product design, and operational support. • Design and implement scalable, production grade data pipelines to support both clinical and operational use cases. • Optimize data ingestion, processing, reliability, and performance to meet the evolving digital demands of the future Neuro Operating Room. • Develop and validate proof-of-concepts and prototype applications to assess feasibility, demonstrate value, and directly inform the Neurotechnology data strategy. • Partner with data, cloud and front-end application engineers to evolve prototypes into reliable enterprise-ready solutions. • Work within Python based data science workflows and enterprise platforms on the Stryker Health Cloud, collaborating closely with advanced R&D, marketing, and external stakeholders. • Write clean, efficient, and well documented Python code for data modelling, data processing, feature engineering, analytics, and visualization supporting next generation neurotechnology products. • Collaborate across disciplines to deliver actionable data-driven insights that drive clinical innovation and operational excellence. Skills needed: • Strong proficiency in Python for data collection, analysis, and data pipeline architecture with an emphasis on scalability.• Proficiency with data visualization standards and tools with a focus on clarity, usability and insight generation. • Ability to ideate and identify, evaluate and integrate novel data sources and explore their potential value in developing clinical insights • Solid foundation in software engineering, electrical engineering, and/or systems engineering fundamentals, enabling effective collaboration across technical disciplines. • Broad, practical experience across the data lifecycle, including strong analytical and problem solving skills, with experience translating complex data into meaningful, real world impact. • Flexible, agile mindset with a systems level design approach, balancing rapid prototyping with long term scalability, reliability and organizational integration. • Bonus: Experience implementing end-to-end AI/ML pipelines, from data ingestion and preprocessing to model training, evaluation, and CI / CD. • Bonus: Hands-on experience with machine learning algorithms and predictive modeling in applied contexts. • Bonus: exposure to deploying optimized, real-time inference models on edge compute systems Requirements: • Bachelor’s degree in Computer Science, Software Engineering, Electrical Engineering, or a related technical discipline • Experience developing data solutions in regulated or clinical environments preferred • 3-5 years of experience delivering solutions in a data architecture, data engineering or related field • Demonstrated experience designing and implementing scalable data models (relational, dimensional, NoSQL) and data warehouse systems • Hands-on experience with modern cloud data platforms (e.g., Databricks) and data governance, lineage, and compliance tooling • Proven ability to excel in cross‐functional collaboration with clinical partners, R&D, IT, and business stakeholders to translate clinical needs into robust, scalable data platform designsTravel Percentage: 10% #J-18808-Ljbffr
