41 jobs in Stryker

Hybrid Role - minimum of 3 days onsite required.
**Key Areas of Responsibility:**
+ Assesses regulatory intelligence to assist in the development of local, regional, and global regulatory strategies
+ Evaluates the regulatory environment and contributes to providing internal advice throughout the product lifecycle (e.g., concept, development, manufacturing, marketing) to ensure product compliance
+ Anticipates regulatory obstacles and emerging issues throughout the product lifecycle and develops solutions
+ Identifies requirements and potential obstacles for market access distribution (federal, provincial/territorial state, reimbursement, purchasing groups, etc.)
+ Assists in the development of regulatory strategy and updates strategy based upon regulatory changes
+ Evaluates proposed products for regulatory classification and jurisdiction
+ Determines requirements (local, national, international) and options for regulatory submission, approval pathways, and compliance activities
+ Provides regulatory information and guidance for product development and planning throughout the product lifecycle to the regulatory groups and others within the organization
+ Compares regulatory outcomes with initial product concepts and recommends changes or refinements based on initial regulatory outcomes
+ Negotiates with regulatory authorities throughout the product lifecycle
+ Identifies the need for new regulatory procedures, SOPs, and participates in development and implementation
+ Helps train stakeholders on current and new regulatory requirements to ensure organization-wide compliance
+ Assists other departments in the development of SOPs to ensure regulatory compliance
+ Provides regulatory input and technical guidance on global regulatory requirements to product development teams
+ Advises stakeholders of regulatory requirements for quality, preclinical, and clinical data to meet applicable regulations
+ Assesses the acceptability of quality, preclinical, and clinical document for submission filing to comply with applicable regulations
+ Evaluates proposed preclinical, clinical, and manufacturing changes for regulatory filing solutions and proposes plans/strategizes (if appropriate) for changes that do not require submissions
+ Provides knowledge and guidance on preapproval inspections, GCP inspections, and clinical investigator relationships
+ Identifies, monitors, and submits applicable reports or notifications to regulatory authorities during the clinical research process
+ Provides regulatory information and guidance for proposed product claims/labeling
+ Ensures that the clinical and nonclinical data, in conjunction with regulatory strategy, are consistent with the regulatory requirements and support the proposed product claims
+ Prepares and submits electronic and paper regulatory submissions according to applicable regulatory requirements and guidelines
+ Monitors the progress of the regulatory authority review process through appropriate communications with the agency
+ Communicates and interacts with regulatory authorities before and during the development and review of a regulatory submission through appropriate communication tools
+ Works with cross-functional teams for interactions with regulatory authorities including panel meetings and advisory committees
**Education / Work Experience:**
+ BS in Engineering, Science, or related degree; or MS in Regulatory Science
+ Typically a minimum of 2 years' experience
+ MS or RAC(s) preferred
**Knowledge / Competencies:**
+ Project management, writing, coordination, and execution of regulatory items
+ Perform technical and scientific regulatory activities
+ Usually works with minimum supervision, conferring with superior on unusual matters
+ Assignments are broad in nature, requiring originality and ingenuity
+ Has some latitude for unreviewed action or decision
\#IJ
Posted Date: 06/18/2026
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

**Project Manager - Advanced Operations**
Tullagreen, Cork (Hybrid)
Permanent Position / Full Time
**Position Summary**
This role is responsible for leading multiple New Product Introduction (NPI) programs, ensuring operational readiness from development through commercialisation. The Project Manager will partner cross-functionally to deliver successful product and process launches aligned to quality, cost, and timeline objectives. While aligned to a primary program, this role requires ownership across multiple concurrent projects and strong critical thinking to drive decisions, manage risk, and ensure execution excellence.
**What You'll Be Doing:**
+ Lead and deliver multiple NPI programs concurrently aligned to business priorities.
+ Own full project lifecycle: scope, planning, execution, monitoring, and closure.
+ Serve as the primary conduit between Global Quality Operations (GQO) partners and Advanced Operations, ensuring alignment and execution.
+ Drive disciplined governance and accountability across programs, ensuring adherence to processes and standards.
+ Ensure successful ramp and robustness by proactively managing risks, readiness, and execution milestones.
+ Lead stakeholder management across key forums, including DTAP, ensuring alignment, transparency, and decision-making.
+ Drive cross-functional collaboration across Quality, Operations, Engineering, Supply Chain, and Commercial.
+ Ensure manufacturing readiness, including process development, validation, and transfer.
+ Manage capital and expense budgets.
+ Establish clear communication plans and provide updates to stakeholders.
+ Identify and manage risks across multiple programs.
+ Drive structured problem solving and data-based decision making.
+ Support operational excellence, DFM, and process optimisation.
+ Foster accountability, urgency, and strong team engagement.
+ Influence without authority
+ Build a culture of transparency and execution excellence.
+ Manage multiple projects concurrently.
+ Champion disciplined governance and stakeholder engagement across GQO and AO interfaces.
**What You'll Need:**
+ Bachelor's degree in Engineering or Science required.
+ 4+ years of experience in project management, engineering, or a technical role in a regulated industry.
+ Experience in New Product Introduction (NPI) required.
+ Strong understanding of manufacturing operations and quality systems.
+ Experience in FDA or regulated environment preferred.
+ Project Management certification preferred.
\#IJ
Posted Date: 06/17/2026
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

**Operations Supervisor - Limerick**
**Swing shift** **= 2 shift cycle**
Days (Mon - Fri) followed by Evenings (Mon - Thurs)
Here at Stryker, we apply our unique strengths, diverse backgrounds, and commitment to quality to develop cutting-edge products for our customers and patients. Our passion, purpose and integrity make us unique. Nowhere else will you find the energy, the opportunities and shared commitment to excel for our customers, for patients and for our family at Stryker. As an Operations Supervisor you will have the opportunity to inspire, lead and mentor diverse teams across our Limerick site. We expect to win as a team by doing things the right way and challenging each other to strive for the very best
**What you will do**
+ Leads Operational Excellence and complex change initiatives across the business. Mentors and develops Supervisors. Deputises for Operations Manager.
+ May have responsibility for Production area(s) and team(s)
+ Leads operations improvement projects and participates in site or campus operational initiatives
+ Under limited supervision, plans, conducts and supervises assignments
+ Reviews progress and evaluates results
+ Recommends changes in procedures and process improvements
+ Accountable for maximisation of resources available to deliver outstanding results on all key performance metrics across the Business unit
+ Deputises for Operations manager and represents Business unit/value stream at site and operations forum
+ May manage a number of production teams to meet customer requirements and deliver KPIs in Quality, Service, Cost and People Development
+ Participates in budget setting for the business unit
+ Drives a proactive and compliant approach to environmental, health and safety
+ Champions 6s process, standards and objectives through coaching, mentoring and setting direction
+ Mentor and coach for Graduate(s) and Operations supervisors.
+ Inspires others by setting the standards, building trust and partnerships, collaborating and encouraging diverse perspectives always acting with integrity
+ Creates a positive employee relations environment and facilitates high engagement across a number of production teams and with cross functional teams
+ Provides timely feedback and review and ensures all performance issues are dealt with in a constructive, fair and prompt manner. Ensures that all employees are treated with fairness and respect
**What you will need**
+ Degree or master's in business, Production Management, Engineering or similar Discipline or demonstrated equivalent experience
+ 4 years minimum experience in a manufacturing environment.
+ 2 years minimum Supervisor experience
+ Supervises Production team(s) or a number of indirect staff
+ Possesses and applies a broad knowledge of principles, practices and procedures of a production environment to the completion of complex assignments
+ Usually works with a minimum of supervision, conferring with leader on unusual matters.
+ Demonstrated leadership aptitude to work with people and set direction as part of a cross functional team and across a large number of teams
+ Excellent knowledge & computer skills in MS Excel, Powerpoint & Word.
+ Business acumen with an ability to deliver process improvement objectives
+ Good knowledge of GMP / FDA regulatory requirements, housekeeping, health and safety.
+ Genuine interest in investing in people and facilitates individual and team engagement and development.
+ Ability to coach, provide effective feedback and manage performance.
+ Problem solving methodology experience required with process knowledge desirable.
+ Can interpret and analyse information and translate into operation actions.
+ Excellent Influencing and communication skills
\#IJ
.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

**Product Development Engineer.**
**Role:** 23 month Fixed Term Contractor
**Location:** Stryker Anngrove, Carrigtwohill, Cork
**Who we want**
+ **Collaborators** - Partners who listen, share thoughts and work together to build and leverage relationships to meet project goals.
+ **Problem solvers** - Critical thinkers who are motivated to solve challenging problems.
+ **Dedicated achievers** - Those who aspire for excellence in a fast-paced environment and take ownership of their work.
+ **Customer-focused** - Engineers who can partner with our customers to drive purposeful innovation, resulting in best-in-class products.
**What you will do**
The Patient Specific Solutions team provides patient-specific devices to those with complex clinical cases, such as oncology cases, where no other device exists on the market to treat their condition. These are provided under the prescription of the overseeing physician in accordance with all applicable laws and regulations for single patient use. As an engineer on the Patient Specific Solutions team, you will perform implant and instrument design work for individual cases. You will be required to liaise with customers including, but not limited to, surgeons, OR staff, clinical staff, distributors, and the sales force, to provide appropriate design solutions for patient-specific orthopaedic devices inclusive of associated instrumentation and supporting documentation. You will deliver this in a timely manner either independently or as part of a team and you will provide technical support to other departments. You will be required to manage your case load under tight time constraints, provide suitable drawings or CAD models for a wide variety of implant types in order to manufacture and inspect, and adhere to procedures set out by Quality and Regulatory Affairs. In some circumstances you may be required to work or travel outside of normal office hours, as well as attend surgical/clinical cases.
**What you will do:**
+ Provide design solutions for a broad range of patient-specific implants inclusive of instruments and trials where necessary;
+ Ensure all solutions meet critical design prerequisites including patient and customer safety, mechanical, and biological suitability;
+ Read and work from various clinical imaging including x-rays, CT, and MRI scans;
+ Provide adequate information via technical drawings and 3D models to manufacturing and inspection (including subcontractor activities such as coating requirements) and prepare job cards and bill of materials (BOMs) with reference drawings as required;
+ Where required, dimension all drawings correctly, apply geometrical tolerancing, finishing and etching details, and carry out tolerance stack calculations;
+ Perform engineering calculations, making reasonable assumptions, to support design validity;
+ Preparation of surgical planning guides/instructions inclusive of appropriate surgical instruments and defining operating instructions for patient-specific implants;
+ Liaise with Design coordinators, Manufacturing Team Leaders and technicians, Product Engineers, Inspectors, Customer Services, QA/RA personnel, and subcontractors with respect to the manufacture and progress of each case;
+ Liaise with consultant surgeons, surgical/OR staff, distributors, and the Sales team with respect to implant design, instrumentation and technical support;
+ Ensure standard templates used for design are current and updated in a timely fashion;
+ Conduct, as part of a team, risk assessments and document all activities and justifications/validations to satisfy regulatory requirements under the guidance of the Quality and Regulatory Affairs counterparts;
+ Attend surgical and clinical cases, as required;
+ Any other tasks that sits outside your current role from time to time to support the activities of the business.
**What you need**
+ Bachelor's degree required; in a science or engineering discipline, Mechanical or Biomedical Engineering preferred.
+ 0-2 years of product design experience in the medical device industry or equivalent.
\#IJ
Posted Date: 06/17/2026
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

This is a 12 month contract role with full Stryker benefits.
Provide Supplier quality engineering support and direction in quality assurance, control and preventative activities within operations and other business functions, with a focus on preventative measures and continuous improvement of products and processes. Advocate and lead the execution of initiatives & projects to enhance quality performance within the business. Ensure compliance to regulation and standards.
**What you will do:**
+ Will work within the quality operations team, under minimal supervision, 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.
+ Oversight and approval of NC & CAPA, activist and mentor in problem solving and root causing activities.
+ Lead and participate in the development and improvement of the manufacturing processes for existing and new products.
+ Analysis and review of concession requests.
+ Review and approval of change management activities.
+ Maintain KPI 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, proficient in the science of Human Factor identification and mitigation.
+ Proficient in risk management practices and tools, having high expertise in process risk. Develop and provide input for risk management by identifying opportunities and weaknesses.
+ Proficiency in and makes continuous strides towards optimization of inspection methods and sampling. Support First Article Inspections.
+ Proficiency in statistical methods and application.
+ Participate and interface in internal & external audits with regulatory representatives, providing effective narrative and description of topic of expertise.
+ Assist in the development, responsible for review & approval of process and equipment validation/qualification.
+ Support manufacturing transfers to other plants/facilities, leading quality activities.
+ Responsible for initiation, management and support of Ship, Product Holds, potential product escapes.
+ Coach and mentor others in quality topics and activities.
**What you will need:**
+ Bachelor degree in Science, Engineering or equivalent/ related subject and 2 or more years of work experience in a quality discipline, or
+ Masters of Science, Engineering or related subject with 0 years of experience
+ Previous experience in a regulated environment desirable.
+ CQE or equivalent course work / experience desirable
+ Proficient in understanding of Med Device manufacturing processes desirable.
+ Familiarity with ISO 13485, GDP, GMP desirable.
Posted Date: 06/16/2026
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

12 month Stryker contract with full benefits.
Will work within the microbiology team, under general supervision, with responsibility to ensure effective and efficient sterility practices, which includes, but not limited to the following:
+ Environmental monitoring of cleanrooms for viable air, viable surface and particulate in line with ISO 14644 standards.
+ Monitoring of utilities including all grades of water, and where necessary, compressed air.
+ Co-ordination of samples for bioburden and endotoxin testing.
+ Ordering consumables (media etc) and general stock for day-to-day running of laboratory.
+ Applying cGLP to all laboratory activities including stock control.
+ Performing sampling for validations and re-qualifications as required. Review of validation files for compliance.
+ Strong interactions, maintainance and support of sterility suppliers.
+ Interact with Supplier quality team with respect to vendor sterility topics.
+ Interpreting sampling and monitoring data, applies statistical and analysis techniques, to determine control and trending.
+ Leads NC and CAPA generation and resolution within the Microbiology group and across related business units. Strong competency in troubleshooting, correction of NC and root cause analysis.
+ Performs sterility release review, interpreting data and trends.
+ Performs sterilisation validations and re-qualifications in line with relevant BS EN ISO standards.
+ Continually identifies opportunity for stabilization of trends, statistical control of processes to allow cost saving.
+ Mentors and trains team and cross functional groups as required (induction, GMP etc)
+ Subject matter expert to internal & external regulatory requirements, (including but not limited to European RHQ, Division, Corporate, FDA, ISO, MDD, and individual country regulatory requirements)
+ Subject matter expert to local procedures, contribute to the development, maintenance and improvements of the policies and procedures to align to best practices, benchmarking against industry leads and regulatory requirements.
+ Coach, mentor and train other functions in area of sterility and monitoring.
+ Support of, ensure compliance of new products to sites' sterility standards. Successful integration of products to validated processes.
+ Ensures biocompatible of components, materials and consumables used in the manufacture of Stryker product.
**What you will need:**
. Bachelor degree/ Masters of Microbiology (Level 8)
. 2 years Microbiology related experience.
Posted Date: 06/16/2026
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

**Position Summary**
Supports and executes design for manufacture and assembly through technical leadership in quality assurance, design control and preventative activities. Supports the development and introduction of new products, processes, and technologies, with focus on quality systems development, regulatory compliance, and process risk management including pFMEA. Support the development and characterization of processes that are capable, scalable and produce high yield. Will support the design of robust inspection strategies including CQA's, CTQ's and MSA's to enable process risk identification, process characterization, capability and robust process control. Provide quality engineering support for the execution of quality assurance activities during design transfer phases of new product development. Provide Quality engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures.
**Position Requirements**
Will reside within the regional NPI QE team as part of GQO Quality Assurance organization and work collaboratively with Advanced Operations and Design Assurance, with responsibility for quality assurance activities, including, but not limited to the following:
General
+ Foster and lead collaborative internal/external professional relationships across Design Divisions, Advanced Operations & GQO functions associated with design transfer activities. Drive and lead effective communication with all internal customers, stakeholders, and project teams to deliver successful project transfers with the highest levels of quality that meet the NPI project goals.
+ Communicate effectively with all internal customers, stakeholders, and project teams to deliver successful project transfers with the highest levels of quality that meet the NPI project goals.
+ Mentor other groups and functions on areas of expertise with particular attention to design and process transfer.
Risk Management
+ Proficient in risk management practices and tools, having high expertise in failure modes associated with production and production related processes, (PFMEA).
+ Support the Risk Management File through risk Management Principles. Responsible for the evaluation of process risks, risk mitigation and ensures appropriate production and process controls are identified, qualified, and implemented throughout the product manufacturing lifecycle (from incoming of materials/components, manufacturing, until product release) through robust pFMEA.
+ Ensure all Risk Management outputs comply with ISO14971.
+ Support Design team to complete CQA/CTQ identification and inputs to dFMEA.
Inspection
+ Develop and implement lean inspection strategies and inspection plans through state-of-the-art inspection methods and technologies. Ensure inspections are repeatable, efficient, and scalable.
+ Lead continuous improvements of inspection methods and sampling plans, with a focus on human error risk elimination.
+ Lead First Article Inspection (FAI) Strategies, both internally and externally, and approve First Article Inspections. Optimize inspection costs through lean initiatives while maintaining safety, integrity, and reliability of the product.
+ Develop Measurement System Analysis (MSA) strategy and approve executed MSAs.
Validation
+ Support the development, execution, and approval of validation strategies, with the goal of highly capable processes, that result in high yield and enable scalability. Approve protocols and reports, including data analysis.
+ Influence processes towards validation versus manual verification, where possible.
+ Support Sterilisation validation activity, as required.
Process Excellence
+ Apply appropriate statistical techniques to ensure the development of robust, predictive quality systems which are easily transferable and maintainable in a production environment.
+ Provide expertise for NC's & CAPA's related to new products. Act as a subject matter expert and mentor in problem solving and root causing tools.
+ Support Design for Manufacture and Assembly (DFMA) through process design, inspection optimization, application of state-of-the-art technologies and tooling & fixture development.
+ Support 'process bench marking' by providing quality experience as a process input.
+ Will promote human factor error prevention and provide expertise in the science of human factor error risk identification and mitigation.
Purchasing Controls
+ Support the supplier qualification strategy and approve the supplier validations and Production Part Approval Process (PPAP). Ensure Supplier's Quality Systems can complete process characterization and develop highly capable processes that are scalable, and meet Stryker expectations.
+ Provide Quality input to influence the proper selection of suppliers.
+ Support implementation of supplier certification.
+ Support Supplier Quality to establish Quality Agreements with Stryker sites and suppliers as part of NPI projects.
Design Transfer
+ Represent quality assurance during the DTAP (Design Transfer Agreement Plan) process, ensuring product launches meet or exceed established metric targets including Right First Time (RFT), manufacturing loss, inspection costs per unit and product escapes, in conjunction with other targets per the DTAP.
+ Provide subject matter expertise in Design transfer processes and procedures, participating and interfacing in internal & external audits with regulatory representatives.
+ Represent NPI Quality Assurance at Design reviews and ensure integrity of the process design through robust NPI quality deliverables.
+ Support device design into production specifications.
**Qualification Knowledge Skills**
+ Bachelor of Science, Engineering or related subject with 4 years' experience in a quality or technical discipline
+ Previous experience in a regulated environment within a manufacturing environment required. 2 years' experience in new product/process is a distinct advantage.
+ CQE or equivalent course work / experience desirable
+ Familiarity with advanced product quality planning framework and techniques used to develop products, a distinct advantage.
+ Proficient in understanding of Med Device manufacturing processes desirable.
+ Familiarity with ISO 13485, QSR, GDP, GMP desirable.
+ Lean Six Sigma training a distinct advantage.
+ Highly proficient in all aspects of Validation. Computer System validation a distinct advantage.
+ Analytical & problem-solving skills, process improvement orientation, and the ability to handle multiple tasks.
+ Competency in Metrology including ability to interpret complex engineering drawings and understand geometrical dimensioning and tolerance.
+ Must be able to generate, follow and explain detailed operating procedures
+ Experience in executing complex problem-solving and process improvements techniques related to design/process/technical issues using lean six sigma tools like DMAIC.
+ Excellent analytical skills, ability to plan, organize and implement concurrent tasks.
+ Excellent interpersonal skills - able to express ideas and collaborate effectively with multidisciplinary teams.
+ Working knowledge/experience of risk based and statistical techniques, in particular process risk, failure mode and effect analysis (FMEA), statistical sampling plans, process capability and MSA's.
+ Manages change well and adopts a continuous improvement mindset
+ Excellent English (both oral and written)
+ Ability to be the voice of quality when dealing cross functionally
\#IJ
Posted Date: 06/16/2026
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

12 month position
**What you will do:**
+ Provide support to R&D, AO and GQO on the development, and verification testing of new and existing products.
+ Develops and coordinates inspection and testing procedures for prototypes, components and products.
+ Formulates test guidelines and procedures and may recommend revisions of specifications where necessary.
+ Set up and perform routine to non-routine experiments of moderate scope which comply with FDA requirements and appropriate engineering standards.
+ Will extract and process test data/findings into both formal written and verbal reports which comply with FDA requirements and appropriate engineering standards.
+ Assists in designing, installing and maintaining process sampling systems, procedures, statistical techniques, testing mechanisms, equipment and fixtures.
+ Evaluates, recommends and maintains engineering related computer systems.
+ Will be required to comply with documentation procedures and maintain test laboratory housekeeping standards to the highest level.
+ Will coordinate with facilities and assist in the maintenance of test equipment and test lab fixtures and fittings.
+ Providing guidance to Co op/Intern, test lab technicians and engineers on test methods
+ Review and approve test reports that meet procedural, technical writing and GDP requirement in the absence of the Lead Technician or on Test Reports where the Lead Technician conducted the testing
**What you will need:**
+ Diploma in an Engineering discipline or relevant experience
+ 2 years test lab experience desirable
+ Must have the ability to work with and assemble small objects and component parts.
+ Must have very good visual acuity and demonstrate fine motor skills.
+ Must be able to observe and correct minute inconsistencies (e.g. in the printed word, product appearance, etc.).
+ Must be able to complete detailed documentation accurately.
+ Must be able to analyze and correct complex testing and/or systems issues of a broad scope using independent judgment.
+ Excellent analytical skills.
+ Excellent interpersonal skills.
+ Advanced computer hardware/software skills.
+ Demonstrated mechanical/electrical problem solving skills.
+ Ability to read, understand and generate complex engineering drawings.
Posted Date: 06/16/2026
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

**The Job's Mission:**
The **Senior Manager Product Marketing** serves as the regional marketing leader responsible for developing and executing a comprehensive marketing strategy across **EMEA** . This role oversees the EMEA marketing organization to strengthen brand presence, accelerate product adoption and support commercial growth across **Peripheral Vascular** markets. Some examples of our product portfolio include **ClotTriever** and **FlowTriever** .
As the primary voice of the EMEA customer, this leader drives market insights, competitive intelligence and structured Voice of Customer (VoC) efforts to identify clinical needs, regional opportunities and barriers to adoption. They translate these insights into actionable recommendations for Global Marketing, Product Management, R&D and clinical teams - ensuring that regional needs are represented in product development and commercialization plans.
This role is based in our **Amsterdam or Ireland locations** : we offer great workplace flexibility with a **hybrid** work model. **This is an exciting opportunity to join one of the world's leading medical technology organizations in our mission of making healthcare better!**
**What you will do:**
+ In your new role, you will start with a familiarization phase to learn about our portfolio and build relationships with internal/external stakeholders.
+ Lead, develop, and inspire a team of approximately 5 direct reports, fostering a growth‑oriented environment and coaching each team member to reach their full potential.
+ In alignment with Global Marketing, define and execute both annual and long‑range marketing and medical education strategies for Peripheral Vascular EMEA, ensuring the organization meets growth, profitability, and market‑share goals.
+ Provide coaching and guidance to your team on effective segmentation, targeting, and positioning to accelerate EMEA adoption of the portfolio.
+ Collaborate closely with EMEA sales leadership to align marketing and commercial priorities, driving market growth and supporting the execution of sales strategies that accelerate portfolio adoption.
+ Lead and oversee regional and country‑level strategies for market access, government affairs and health‑economics initiatives across EMEA, collaborating closely with key stakeholders to deliver business‑enabling solutions for the sales organization.
+ Develop/refine metrics to evaluate the impact of marketing efforts on customer engagement and build deep P&L expertise to understand and influence the financial performance of the Peripheral Vascular business in EMEA.
+ Capture key market dynamics, customer feedback & insights as well as Voice of Customers (VoC) trends related to EMEA's specific needs and considerations.
+ Define and execute regional product life cycles, including launch and phase-out of products.
+ Identify opportunities and influence cross-regionally and cross-divisionally to drive growth and deliver enhanced customer value for our business.
+ Collaborate with the Global Marketing team including upstream and downstream marketing projects.
**What you need:**
Required:
+ Bachelor's degree is required.
+ 10+ years of work experience is required, of which a significant portion is in fields such as international Marketing, Product/Brand Management etc. within industries such as MedTech, BioTech, Pharmaceuticals, healthcare or related.
+ Experience in managing or coaching/mentoring teams is **required** (4+ years is preferred).
+ Ability to accurately and effectively lead/manage (marketing) projects to ensure timely outcomes, business performance and growth.
+ Excellent interpersonal communications, persuasion and presentation skills - with fluency in spoken and written **English** .
+ You are a sophisticated collaborator and networker capable of leveraging these strengths and relationships effectively within a matrixed organization.
+ Demonstrated ability to relate to stakeholders and customers from different markets and cultures.
+ Strong strategic-thinking, analytical and problem-solving skills.
+ Ability to understand and work within complex interdivisional procedures and policies.
+ Impeccable work ethics & integrity in managing confidential information.
+ Demonstrated proficiency in Microsoft Office (Excel, Word & PowerPoint).
+ Travel percentage: up to 50%.
Preferred:
+ Working experience in the Interventional Cardiology, Interventional Radiology or Vascular Surgery field is not mandatory, but would be an advantage.
+ MBA is preferred.
**What we offer:**
+ Flat hierarchies and a culture committed to achieve our mission and deliver remarkable results.
+ We grow talent: we offer great personal and internal career development for our employees, with the possibility to make both vertical and lateral position movement.
+ An attractive salary and benefits package.
+ Recognition of your performance: at Stryker, outstanding individual and cross-functional team performance is rewarded. Ideas, projects, or other exceptional achievements can be submitted for various awards on a local and global level.
+ Collaborative and inclusive environment: join a team that values diversity and inclusion, fostering a supportive and innovative workplace.
+ Quality products that improve the lives of our customers and patients.
+ Ability to discover your strengths, follow your passion and own your career.
\#li-hybrid
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.