28 Manufacturing jobs in Cork

Purpose of Role:
The Manufacturing Engineer (ME) will provide engineering and process support to ensure successful implementation of 2D barcoding in line with EU MDR requirements.
This role will focus on supporting technical strategy execution, process validation, and operational readiness across both internal manufacturing and supplier sites.
Key Responsibilities:
+ Support technical execution of 2D barcode implementation, including validation activities (VP, IQ, OQ, PQ).
+ Partner with Quality Engineers (QEs) and Supplier Quality Engineers (SQEs) to assess and confirm laser marking equipment compatibility and process qualification at both supplier and internal sites.
+ Assist in First Article Inspection (FAI) preparation, reviewing supplier provided verification data and ensuring compliance to marking requirements.
+ Update and maintain manufacturing documentation (DCP, PFMEA, SOPs) to reflect new barcoding processes.
+ Collaborate with operations teams to ensure inspection readiness (visual inspection, barcode verifier checks).
+ Troubleshoot and provide technical support during initial marking trials and confidence runs.
+ Support scrap management, label obsolescence, and carton switchovers as required for Go-Live phases.
+ Actively contribute to risk assessments, ensuring process robustness and alignment with MDR and GMP requirements.
Required Skills & Experience:
+ 2-4 years' experience in a regulated manufacturing environment (medical device preferred).
+ Exposure to process validation and FAI/PPAP activities in a regulated environment.
+ Familiarity with laser marking or UDI/2D barcoding processes desirable.
+ Strong problem solving and root cause analysis capability (Six Sigma / Lean tools beneficial).
+ Proven ability to work collaboratively with cross functional teams (QE, SQE, and Operations).
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.

Job Description Our client in Cork and Galway require experienced Manufacturing Engineers to support an upcoming project. This role will focus on manufacturing process validation, quality system updates, and documentation remediation. You will be based onsite and work directly with manufacturing and quality process owners to identify compliance gaps, implement corrective actions, and ensure documentation is accurate and audit-ready. Key Responsibilities Analyse process, product, material or equipment specifications and performance requirements Under broad supervision / guidance compile and analyse operational, test and experimental data to establish performance standards for newly implemented or modified products / processes Summarise, analyse and draw conclusions from test results leading to effective technical resolution Troubleshoot new products / process working closely with product development Continually seek to drive / improvements in process design, layout and operational performance Demonstrate good working knowledge and application of validation techniques and associated regulatory requirements Actively promotes and participates in a cross -functional teamwork environment Evaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects Understands and comply with all the regulations governing the quality systems Key Requirements Engineering or Quality degree with 2-3 years' relevant industry experience Background in remediation, process validation, CAPA, NCRs. Strong technical writing and documentation skills. Knowledge of 21 CFR Part 820, ISO 13485. Benefits Competitive and attractive employee compensation package Pension contributions Health insurance Paid public holidays Location:Cork and Galway, Ireland | onsite Skills: Manufacturing Validation CAPA NCR Benefits: Paid Holidays Pension Health

Are you a Quality/Manufacturing engineer looking for a new opportunity? Don't hesitate and apply today! PROJECT DESCRIPTION We are seeking experienced Remediation Quality Engineers / Manufacturing Engineers to support a site-wide remediation program following an FDA 483. These roles will focus on manufacturing process validation, quality system updates, and documentation remediation. Consultants will be based onsite and work directly with manufacturing and quality process owners to identify compliance gaps, implement corrective actions, and ensure documentation is accurate and audit-ready. The project will involve tackling remediation areas in sequence, updating technical files and procedures, and ensuring robust validation of manufacturing processes. Consultants must be able to take a problem statement through to a compliant solution, collaborating cross-functionally across Quality, Manufacturing, and Regulatory teams. PROJECT DESCRIPTIONPartner with process owners on the floor to capture and remediate issues.Support process validation (IQ/OQ/PQ) and documentation updates.Drive CAPA/NCR closure and implement compliant solutions.Provide technical writing for quality and manufacturing documents.Collaborate cross-functionally to ensure regulatory compliance. CONSULTANT RESPONSIBILITIESEngineering or Quality degree with 5-10 years' med-tech experience.Background in remediation, process validation, CAPA, NCRs.Strong technical writing and documentation skills.Knowledge of 21 CFR Part 820, ISO 13485.LOCATION: Cork

**Senior Manufacturing Engineer**
**Contract:** Permanent + full suite of benefits
**Location:** Model Farm Road, Cork
**Business Area:** Neurovascular ( Position**
**About Stryker**
We are excited to be named one of the _World's Best Workplaces_ by **Fortune Magazine!**
We are proud to offer you our **comprehensive rewards package** , which includes bonuses, healthcare, insurance benefits, retirement programs, wellness initiatives, and service recognition programs.
**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. You will be responsible for driving process efficiency and continuous improvement across all stages of complex assembly operations, ensuring validated manufacturing systems consistently deliver exceptional product quality and operational excellence.
**Key Responsibilities:**
+ Own and sustain **manufacturing processes within value streams** for Neurovascular products, ensuring product quality, process stability, and regulatory compliance.
+ Lead root cause analysis and implement corrective to address product and process issues.
+ Identify and deliver **continuous improvement (CI) and cost reduction** projects focused on **OEE, yield, and scrap reduction** , applying Lean, Six Sigma, and statistical techniques.
+ Execute **process and equipment changes** under Stryker's quality system, including documentation, risk assessment, validation, and change control.
+ Support ongoing **process validation (IQ/OQ/PQ)** and maintain a validated state through periodic reviews and revalidations as required.
+ Partner with **Production, Quality, Maintenance, and Supply Chain** teams to improve equipment uptime, throughput, and reliability.
+ Lead **data collection, analysis, and reporting** on key performance metrics (yield, downtime, cost per unit, etc.) and drive improvements based on findings.
+ Support and lead **audits, CAPA closure, and documentation updates** to ensure compliance with ISO 13485 and FDA QSR standards.
+ Train and mentor technicians and operators on process changes, standard work, and best practices to foster a culture of continuous improvement.
+ Contribute to cross-site collaboration, sharing best practices and lessons learned across Stryker's Cork and global manufacturing network.
**Qualifications, Knowledge & Skills**
+ Bachelor's degree (or equivalent) in **Manufacturing, Mechanical, Industrial, or Biomedical Engineering** (or related discipline).
+ Minimum **2** **+ years of experience** in **manufacturing or process engineering** , ideally in a **regulated medical device** or **high-volume precision assembly** environment.
+ Proven expertise in **continuous improvement, process optimisation, and problem solving** (Lean/Six Sigma Green Belt preferred).
+ Strong understanding of **manufacturing documentation** , **change control** , and **validation processes** .
+ Solid experience with **CAPA management** , risk analysis (PFMEA), and troubleshooting production issues.
+ Excellent interpersonal and communication skills with the ability to influence and work cross-functionally.
+ Strong technical judgment and a hands-on approach to resolving complex engineering challenges.
**Why Join Stryker Cork**
+ Be part of a world-class **Neurovascular manufacturing hub** focused on precision, safety, and innovation.
+ Collaborate with a talented, diverse team committed to operational excellence.
+ Grow your career in a **globally** **recognised organisation** that invests in its people and values integrity, accountability, and inclusion.
+ Thrive in a culture that celebrates teamwork, continuous improvement, and life-changing innovation.
#IJ
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.

**Staff Manufacturing Engineer (Value Chain)**
**Contract:** Permanent + full suite of benefits
**Location:** Model Farm Road, Cork
**Business Area:** Neurovascular ( Type:** On-Site
**About Stryker**
We are excited to be named one of the World's Best Workplaces by Fortune Magazine!
We are proud to offer you our comprehensive rewards package, which includes bonuses, healthcare benefits, insurance, retirement programs, wellness initiatives, and service recognition programs.
**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. You will be responsible for driving process efficiency and continuous improvement across all stages of complex assembly operations, ensuring validated manufacturing systems consistently deliver exceptional product quality and operational excellence.
**Key Responsibilities**
+ Own and sustain **manufacturing processes within the value streams** for Neurovascular products, ensuring product quality, process stability, and regulatory compliance.
+ Lead **root cause analysis** and implement **corrective** to address product and process issues.
+ Identify and deliver **continuous improvement (CI) and cost reduction** projects focused on **OEE, yield, and scrap reduction** , applying Lean, Six Sigma, and statistical techniques.
+ Execute **process and equipment changes** under Stryker's quality system, including documentation, risk assessment, validation, and change control.
+ Support ongoing **process validation (IQ/OQ/PQ)** and maintain a validated state through periodic reviews and revalidations as required.
+ Partner with **Production, Quality, Maintenance, and Supply Chain** teams to improve equipment uptime, throughput, and reliability.
+ Lead **data collection, analysis, and reporting** on key performance metrics (yield, downtime, cost per unit, etc.) and drive improvements based on findings.
+ Support and lead **audits, CAPA closure, and documentation updates** to ensure compliance with ISO 13485 and FDA QSR standards.
+ Train and mentor technicians and operators on process changes, standard work, and best practices to foster a culture of continuous improvement.
+ Contribute to cross-site collaboration, sharing best practices and lessons learned across Stryker's Cork and global manufacturing network.
**Qualifications, Knowledge & Skills**
+ Bachelor's degree (or equivalent) in **Manufacturing, Mechanical, Industrial, or Biomedical Engineering** (or related discipline).
+ Minimum **4+ years of experience** in **manufacturing or process engineering** , ideally in a **regulated medical device** or **high-volume precision assembly** environment.
+ Proven expertise in **continuous improvement, process optimisation, and problem solving** (Lean/Six Sigma Green Belt preferred).
+ Strong understanding of **manufacturing documentation** , **change control** , and **validation processes** .
+ Solid experience with **CAPA management** , risk analysis (PFMEA), and troubleshooting production issues.
+ Excellent interpersonal and communication skills with the ability to influence and work cross-functionally.
+ Strong technical judgment and a hands-on approach to resolving complex engineering challenges.
**Why Join Stryker Cork**
+ Be part of a world-class **Neurovascular manufacturing hub** focused on precision, safety, and innovation.
+ Collaborate with a talented, diverse team committed to operational excellence.
+ Grow your career in a **globally recognised organisation** that invests in its people and values integrity, accountability, and inclusion.
+ Thrive in a culture that celebrates teamwork, continuous improvement, and life-changing innovation.
#IJ
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.

**Senior Engineer, Manufacturing**
Contract: Permanent Contract
Location: Tullagreen, Carrigtwohill
On-Site Position
**Position Summary:**
The senior Engineer will Provide advanced technical and engineering support to a project or function. This engineer will have the required engineering competencies and systems training to support a manufacturing area or project.
**Key Areas of Responsibility:**
+ Application of a prioritised approach in Value Centred Engineering toward achieving key opportunities in quality, service and cost.
+ Works with Engineering leaders to deliver business objectives
+ 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 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.
**Qualifications Knowledge Skills:**
+ Level 8 Degree in Mechanical Engineering or equivalenttechnical experienceis required.
+ Proven Project Management skills through the delivery of business critical projects.
+ Has 2-4 years' experience in a manufacturing environment.
+ Strong communication and influencing skills with both internal and external agents.
+ Capable of technical leading, influencing and providing technical direction to Engineers, Coop Students, Technicians and operators as required.
+ Capable of working as part of a multi-disciplined team in an aggressive, dynamic and results motivated environment
+ Demonstrable analytical & problem solving skills, a process improvement orientation, and the ability to handle multiple tasks in a fast-paced and results-oriented environment
+ Excellent presentation and written / verbal communication skills
+ Demonstrable ability to work autonomously
+ A team player, with a flexible approach.
+ Technological pioneer, willing to source, investigate and implement technological and automation advances
+ Confident and effective decision maker, with a proven leadership ability to negotiate and influence others.
#IJ
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.

**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 effectively builds the products manufactured by Stryker to the required quality standard
**What you will do**
+ Responsible for manufacturing product in accordance with the relevant Stryker manufacturing procedures and relevant quality standards
+ Participation in continuous improvement programmes or team projects to enhance our quality customer service and cost
+ Monitor and verify quality in accordance with workmanship standards and operating procedures
+ Adhere to procedures in relation to production methods, completion of documentation, current Good Manufacturing Practices and safety requirements
+ Provide cross training to other employees
+ Contribute as part of a team in achieving the line core metrics
+ Build Quality into all aspects of their work by maintaining compliance to all quality requirements
**What you need**
+ Leaving Certificate, Trade or equivalent education level is required
+ Previous experience in production/ assembly roles is desirable
+ Basic mathematics and good English skills
+ Good communication skills
+ Willingness to work in a team and promote teamwork
+ Previous experience in production/ assembly roles is an advantage
+ The employee may be required to use protective clothing and safety equipment such as safety glasses and respirators, and the use of personal protective equipment (PPE)
**Please note this is a fully onsite role based in our Macroom manufacturing site. This role may be suitable for someone commuting from Cork City or Kerry.**
#IJ
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.

Senior Engineer, Manufacturing Contract: Permanent Contract Location: Tullagreen, Carrigtwohill On-Site Position Position Summary: The senior Engineer will Provide advanced technical and e ngineering support to a project or function . This engineer will have the required e ngineering competencies and systems training to support a manufacturing area or p roject . Key Areas of Responsibility: Application of a prioritised approach in Value Centred Engineering toward achieving key opportunities in quality, service and cost. Works with Engineering leaders to deliver business objectives 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 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. Qualifications Knowledge Skills: Level 8 Degree in Mechanical Engineering or equivalent technical experience is required. Proven Project Management skills through the delivery of business critical projects. Has 2-4 years' experience in a manufacturing environment. Strong communication and influencing skills with both internal and external agents. Capable of technical leading, influencing and providing technical direction to Engineers, Coop Students, Technicians and operators as required. Capable of working as part of a multi-disciplined team in an aggressive, dynamic and results motivated environment Demonstrable analytical & problem solving skills, a process improvement orientation, and the ability to handle multiple tasks in a fast-paced and results-oriented environment Excellent presentation and written / verbal communication skills Demonstrable ability to work autonomously A team player, with a flexible approach. Technological pioneer, willing to source, investigate and implement technological and automation advances Confident and effective decision maker, with a proven leadership ability to negotiate and influence others. #IJ This role will be posted for a minimum of 3 days. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.

A Senior Manufacturing Engineer is required by CareerWise Recruitment for our Cork based MN client. This is a technical leadership role working across many highly technical disciplines. THE ROLE: * Develop detailed understanding of best practice in product/process performance within the Medical devices industry. * Develop support network of key divisional/corporate leaders academic and supplier partners to enhance understanding of product manufacture and quality * Drive high levels of employee engagement through a highly effective support structure implemented for all engineers. * Develops technical solutions to complex technical problems where analysis of situations requires an in depth evaluation of variable factors. * Serve as technical advisor to engineering personnel. REQUIREMENTS: * Minimum of Level 8 Degree in an Engineering discipline Masters/ black belt an advantage * 6 plus years manufacturing experience with increasing levels of responsibility * Excellent communication and influencing skills with both internal and external agents. * Capable of technically leading a multi-disciplined team in a fast paced, dynamic and results motivated environment Please call Diarmuid Buckley today for further information on or email: CareerWise Recruitment (In Search of Excellence) Established in 1999, CareerWise Recruitment specialises in recruitment of management and technical professionals for the life sciences, ICT, engineering, food and agri sectors. We operate out of multiple locations in Ireland and have offices inCork,Shannon,Galway,Mayo and Dublin. By applying for this position, you are consenting to allow CareerWise Recruitment to process and retain your data in accordance with our Privacy Policy, contained on our website for the purposes of providing career opportunities. CareerWise Recruitment accepts that you do not wish your personal data, including your CV, to be forwarded to any client company without your prior consent and gives an absolute assurance that this wish will always be respected. Please feel free to contact us if you have any queries or wish to withdraw or amend your consent. Skills: Senior Principal Manufacturing