Manufacturing Engineer – Cork
Contract: Permanent + full suite of benefitsLocation: Model Farm Road, CorkBusiness Area: Neurovascular (On‑Site)
Position Overview: In this role, you will play a key part in developing, optimising, and sustaining manufacturing processes for advanced neurovascular medical devices used in the treatment of strokes and aneurysms. The position demands a strong emphasis on precision, process reliability, and adherence to stringent regulatory and quality standards.
Key Responsibilities:
Ensure quality of process and product as defined in the appropriate OS and Material specifications.
Ensure GMPs and system safety.
Participate in FMEA, Control Plan, SOP and PPAP generation associated with product transfers and scale‑ups.
Support capital acquisition activity from specifying equipment, contract negotiation, installation, and validation.
Provide training for manufacturing team members.
Interface with Materials Science, Design and Quality Assurance departments to provide customers with a quality product in a timely manner.
Validation, appraisal, and support of coating suppliers, machining suppliers and raw material suppliers, e.g., forgings, titanium, etc.
Communicate and participate in system and process troubleshooting with support team members and with external agents.
Lead and participate in cross‑functional and cross‑divisional process improvement initiatives.
Provide engineering support for new Product and new process introduction, ensuring that all activities are completed and documented in accordance with Stryker's New Product Development Process.
Process validation for products and processes; VP, IQ, OQ, PQ and associated documentation.
Conduct Gauge R&R studies for products and new processes.
Carry out structured problem solving.
Application and development of statistical tools for use in driving continuous improvement projects.
Provision of out‑of‑hours support to the business as required by management or as mandated by shutdowns and/or equipment failures.
All other duties as assigned.
Qualifications, Knowledge & Skills:
Level 8 Degree in Engineering, Science, or a related discipline, or equivalent technical experience.
Have 0-2 years of experience in a manufacturing environment.
A solid understanding of operations and their impacts is essential.
Strong communication skills with both internal and external stakeholders.
A self‑starter with demonstrated efficient work methods, analytical and problem‑solving skills, and the ability to manage multiple tasks in a fast‑paced environment.
Experience in an FDA‑regulated or similar industry is beneficial.
Experience in a Six Sigma and Lean Manufacturing environment with proven improvement results.
Green or Black Belt Six Sigma qualifications.
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.
Posted Date: 03/26/2026 – This role will be posted for a minimum of 3 days.
Senior Manufacturing Engineer – Cork
Contract: Permanent + full suite of benefitsLocation: Model Farm Road, CorkBusiness Area: Neurovascular (On‑Site)
Position Overview: In this role, you will play a key part in developing, optimising, and sustaining manufacturing processes for advanced neurovascular medical devices used in the treatment of strokes and aneurysms. The position demands a strong emphasis on precision, process reliability, and adherence to stringent regulatory and quality standards.
Key Responsibilities:
Application of a prioritised approach in Value Centred Engineering toward achieving key opportunities in quality, service and cost.
Responsible for assisting in the development of a world‑class manufacturing group that is proficient in process improvement and problem‑solving manufacturing issues using Six‑sigma tools.
Providing technical leadership on all product and process issues.
Line performance monitoring, and the compilation and execution of structured event plans to remediate systemic issues that drive sub‑optimal performance.
Development and implementation of appropriate supporting documentation, SOPs and process work instructions compliant with current Good Manufacturing Practices (GMP).
Leading technical improvements under the business's Continuous Improvement Program (CIP).
Transferring and implementing processes, either from development or from another manufacturing facility.
Provision of technical leadership/guidance for the Process/maintenance Technicians and other Manufacturing / Equipment Engineers on the team.
Provide engineering support for new Product and new process introduction, ensuring that all activities are completed and documented in accordance with Stryker's New Product Development Process.
Process validation for products and processes; VP, IQ, OQ, PQ and associated documentation.
Conduct Gauge R&R studies for products and new processes.
Carry out structured problem solving.
Responsibility for projects (value stream and cross‑functional) as assigned by the company, including the scoping, approval, budgeting, specification, execution, qualification and operational handover as appropriate.
Actively interfacing with cross‑functional team members and 3rd party Vendors, and always practising good teamwork in support of the day‑to‑day operating requirements, and in pursuit of achieving the business targets.
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.
Continuous monitoring and reporting of variables that feed into the business performance metrics, and proactive identification and resolution of issues around any deficits in the same.
Adherence to, and enforcement of all Environmental Health and Safety (EHS) requirements on site.
Elimination and/or management of material risks on the production floor in co‑operation with Supplier Quality engineers.
Undertaking, where appropriate, a Subject Matter Expert's role for Regulatory Audit purposes.
Provision of out‑of‑hours support to the business as required by management or as mandated by shutdowns and/or equipment failures.
All other duties as assigned.
Qualifications, Knowledge & Skills:
L8 Bachelor's degree (or equivalent) in Mechanical, Manufacturing, Precision Engineering or related engineering discipline.
Minimum 2+ years of relevant industry experience.
Passion for Manufacturing Technology / Supplier Development in a regulated environment.
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 a Lean Six Sigma mindset are advantageous.
Experience in executing complex problem‑solving techniques related to manufacturing/design technical issues. Good instincts and sound judgement for mechanical and structural design. Photonics.
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 industry is beneficial.
Excellent attention to detail.
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.
Posted Date: 03/26/2026 – This role will be posted for a minimum of 3 days.
Packaging Solutions – Life Cycle – Cork
Position Summary: Leads the packaging solutions life cycle process (post launch assess phase) for legacy product packaging design by providing technical support for our internal Customer network. This includes the ownership of any packaging design related issues such as PER's, NCR's and CAPA's and leading such exercises as consolidation activities and other package design cost reduction projects. This will ensure we continue to provide high quality, cost effective and fully compliant Medical Device packaging to our Customers.
What you will do:
Lead the post launch assess phase activities of all product packaging design solutions for Recon products.
Provide technical support to both the Quality Assurance and Regulatory teams to help investigate and recommend solutions to any package / labelling design related issues and the completion of technical assessments where applicable.
Own all package design related NCR/CAPA's for the Packaging Solutions Group and ensure timely closure of all issue in line with corporate guidelines.
Take the VOC (voice of the customer) for packaging be it through a request for change, complaint (PER) or general inquiry etc. and transfer it into appropriate action with regards packaging design ensuring proactive and satisfactory closure with the customer.
Completion of the associated risk documentation for Packaging.
Provide technical support to Packaging Operations to help troubleshoot, investigate, and recommend solutions to any package / labelling design related issues.
Provide technical support to the Supply Chain team on any package / labelling design related supplier issues or re‑sourcing activities.
Interface with the Global PSE Packaging Group and other PSE team members both locally and globally, Quality Assurance / Regulatory and Operations Teams to ensure equivalency of approach in Equipment, Processes and Validation techniques.
Expected to lead and provide strategic direction and support to the PSE Packaging Solutions Group.
Provide direction to other members of the PSE Packaging Group in complex or difficult situations, address obstacles, identify resource needs and interact with other areas of the business to assist team in overcoming problems and streamlining the work process.
Provide strategic direction in relevant areas of responsibility on packaging development and new process efforts.
Assist in the establishment of priorities, imparting a sense of urgency and importance to effective project management and delivery of projects to the market on time and within the right cost structure.
Model team values and demonstrate enthusiasm and commitment to the PSE Packaging Groups organisational vision, high degree of participation in problem solving and decision making both locally and globally.
Provide mentoring where applicable to the other members of the PSE Packaging Group.
What you will need:
Degree or Higher in Engineering, Science or Business discipline.
The individual must have a minimum of 2 years relevant packaging experience within a regulated environment.
Business understanding of operations and their individual impact is essential.
Strong communication skills with both Internal and external agents.
Flexibility essential with strong project management skills.
The individual should enjoy working in a dynamic and results motivated team based.
Self starter with demonstrated efficient work methods, analytical & problem solving skills and ability to handle multiple tasks in a fast paced environment.
PC literate and strong knowledge of Microsoft Office tools are essential.
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.
Posted Date: 03/23/2026 – This role will be posted for a minimum of 3 days.
Cadence – Product Engineer II – Cork Office
Job Overview: We are looking for an RF/microwave design engineer with experience using Microwave Office software or other high‑frequency electronic design automation (EDA) software tools who is interested in software development and validation.
Job Responsibilities:
Work closely with research and development on new feature development.
Developing automated testing infrastructure.
Provide technical assistance and training on the use of the AWR Design Environment software products.
Assist in the implementation of AWR software into the customers' design methodologies.
Support technical evaluations as well as benchmarks.
Verify that software enhancements adequately address their target problems.
Job Qualifications:
MS in Electrical Engineering, Computer Engineering, or related field and 3+ years of relevant industry experience (preferred).
RF/MW circuit design coursework or industry experience.
Experience with Python programming language.
Excellent oral and written communication skills.
Additional Skills/Preferences:
Proficiency in a Linux environment.
Experience with Cadence Virtuoso or Allegro would be highly desirable.
Experience with EM Simulation software.
Experience with automated software testing.
Cadence is a global leader in electronic design automation and is committed to equal employment opportunity throughout all levels of the organization.
Stantec – Process Engineer – Ireland
Position Overview: As a Process Engineer, you will play a key role in delivering water treatment solutions across a range of projects. You will lead the process and detailed design of treatment systems, carrying out and reviewing process calculations, mass balances and performance assessments to develop efficient and reliable solutions.
Key Responsibilities:
Coordinate with engineers and external stakeholders to review contractor and vendor submissions.
Support project managers with technical input on risk, cost and programme.
Ensure compliance with regulatory, safety and quality standards.
Lead process and detailed design of treatment systems, carrying out process calculations, mass balances, and performance assessments.
Communicate design decisions and recommendations to project stakeholders.
Qualifications:
Bachelor's degree in civil, Environmental, Chemical or Process Engineering, or a related discipline.
Chartered Engineer status, or working towards chartership (or equivalent professional registration).
Proven experience designing water and wastewater treatment infrastructure, ideally delivering projects for Uisce Éireann or other water utilities.
Strong technical knowledge of water engineering principles, standards, regulations and industry best practice.
Stantec is an inclusive and collaborative environment, offering competitive salary, enhanced pension plan, private medical insurance and other benefits.
Red Hat – Senior Product Security Engineer
Position Summary: The Red Hat Product Security Compliance team is seeking a knowledgeable and proactive Senior Product Security Engineer to achieve our security and compliance objectives. The team is growing and we have a big vision particularly as it relates to burgeoning digital sovereignty laws and efforts worldwide.
What you'll be doing:
Own the security and compliance functions related to our digital sovereign commercial product offerings and environments.
Lead technical discussions across multi‑functional engineering teams, product and sales teams, as well as with third‑party auditors.
Support the continuous improvement of Red Hat Product Security through designing, developing, and implementing automation at scale.
Mentor and aid the growth of junior team members.
Support the downstream integration of open‑sourced projects; collaborate to develop and implement Red Hat specific capabilities from the upstream.
Serve as an evangelist of security and compliance both inside Red Hat and externally, with partners, customers, or within the open‑source community.
What you will bring:
Experience working with Kubernetes, OpenShift, Podman, or similar technologies.
Demonstrable knowledge of applying cloud security principles and best practices to a cloud or hybrid cloud environment.
Have developed and delivered secure and attested software in programming languages such as Go and Python is a plus.
Experience using AI tools like Cursor AI, Claude, or others to accelerate product development delivery timelines.
Ability to analyze security controls, assess risks, and design control measures in alignment with a variety of standards and frameworks (NIST 800‑53, PCI DSS, ISO 27001, etc.).
Proven track record of being effective when working remotely with a global organization and in a self‑directed capacity.
Strong communication skills, capable of presenting technical compliance concepts to both technical and non‑technical audiences.
Relevant certifications, such as CISSP, CISM, CCSP, or CISA, are a plus.
Experience with open‑source software is a plus.
Red Hat is a global leader in enterprise open source, committed to an inclusive and equal‑opportunity workplace.
Senior Process Development Engineer – Advanced Operations – 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 Responsibilities:
Lead Supplier PPAPs (Production Part Approval Process) for various components / complex assemblies, ensuring supplier(s) meet Stryker requirements for NPI.
Work with NPI team (Design, Quality, Manufacturing, Operations) and suppliers to develop & agree PPAP plan detailing supplier‑specific requirements for part/product characterisation, qualification, and launch readiness, e.g.
Validation (IQ/OQ/PQ), Process & quality control activities, Process capability studies, Measurement system analysis studies, Material certifications, Sample production parts/prototypes, Environmental compliance REACH / ROHS, Manufacturing capacity assessments, All other supporting documentation.
Lead supplier PPAP meetings, drive accountability, technical rigour, and adherence to deliverables.
Apply lean / Six Sigma problem‑solving methodologies.
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 First Article Inspections & capability studies for process control and generate subsequent production documentation, ensuring that all activities are completed and documented in accordance with Stryker's new product development procedures.
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:
L8 Bachelor's degree (or equivalent) in Mechanical, Manufacturing, Precision Engineering or related engineering discipline.
Minimum 2+ years of relevant industry experience.
Passion for Manufacturing Technology / Supplier Development in a regulated environment.
Must be able to read and interpret complex engineering drawings and have the ability to understand geometrical dimensioning and tolerancing.
Excellent interpersonal skills – must 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 envisage new and better ways of doing things. Continuous improvement and a Lean Six Sigma mindset are advantageous.
Experience in executing complex problem‑solving techniques related to manufacturing/design technical issues. Good instincts and sound judgement for mechanical and structural design. Photonics.
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 industry is beneficial.
Excellent attention to detail.
Stryker 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.
Posted Date: 02/25/2026 – This role will be posted for a minimum of 3 days.
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