What Jobs are available for Manufacturing in Cork?

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Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing – whatever your ambitions.

Purpose Statement

To support the engineering and implementing of highly capable & effective manufacturing processes to meet business goals and objectives.

Key Responsibilities

• To support the key activities utilized in quality, service & cost improvements in the Operations Engineering Cycle to meet key business objectives.
• To support a prioritised approach in Value Centred Engineering to achieve the key opportunities in quality, service and cost.
• Production line monitoring and the identification and quantification of process problems, along with subsequently implementing the necessary improvements and/or controls.
• Liaising with the Quality and Operations functions in pursuit of achieving the quality and S&OP targets for each given area.
• Participation in cross-functional projects works as dictated by the emerging business needs.
• Taking direction from Manufacturing Engineer II's and Senior Engineer's as to how best to deploy resources and effort on the operations floor.
• Actively seek ways and means of increasing efficiency, productivity, yield and space utilisation on the operations floor.
• Manage material risks, as identified by the business.
• Always Observe the Quality Management Systems requirements on site.
• Communicate regularly with the Product Builders regarding issues, concerns and watchouts on the lines.
• Work closely with our in-house Equipment Design & Engineering workshop in getting equipment/fixtures designed & fabricated.
• Development and implementation of appropriate supporting documentation which complies with Good Manufacturing Practices (GMP) in conjunction with other team members.
• Leading technical improvements under the site's continuous improvement program.
• Actively interfacing with cross-functional team members, always practicing good teamwork in support of day-to-day operating requirements.

Education & Experience

• Level 8 Honours Batchelors degree in a relevant Engineering or Science discipline.
• Strong communicator with excellent problem-solving skills.
• Teamwork & collaboration is a key competency for this role.
• Ideally experience of working in a regulated environment.

Requisition ID:

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.

So, choosing a career with Boston Scientific (NYSE: BSX) isn't just business, it's personal. And if you're a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you

Work Flexibility: Hybrid

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).

Travel Percentage: 10%

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.

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.

We are recruiting a Manufacturing & Quality Engineer for our clients in County Cork. The role focuses on improving manufacturing processes, ensuring high-quality production standards, and supporting product innovation. The successful candidate will work closely with production, R&D, and quality teams to deliver consistent, efficient, and reliable manufacturing operations. This is a full time, permanent position based within easy commute of both Killarney and Macroom.

Key Responsibilities

• Monitor and improve manufacturing processes to enhance efficiency, safety, and product quality.
• Develop, implement, and maintain quality control procedures and standards across production lines.
• Conduct root cause analysis for production and quality issues and implement corrective actions.
• Support new product introductions, ensuring manufacturability and quality compliance.
• Collaborate with R&D and engineering teams to optimize production processes.
• Perform audits, inspections, and testing to ensure compliance with internal and regulatory standards.
• Maintain accurate documentation for quality records, production reports, and continuous improvement initiatives.
• Provide training and guidance to production staff on quality procedures and best practices.

Key Requirements

• Degree or Diploma in Mechanical, Manufacturing, Industrial, or Quality Engineering.
• Minimum 2–3 years' experience in manufacturing or quality engineering, preferably in the HVAC, appliance, or FMCG sectors.
• Strong knowledge of lean manufacturing, Six Sigma, and continuous improvement methodologies.
• Familiarity with quality standards such as ISO 9001 and regulatory compliance.
• Excellent problem-solving, analytical, and communication skills.
• Proficient in ERP systems, Microsoft Office, and data analysis tools.

Salary is open to negotiation, based on experiences. For further information, please email me directly

About the Opportunity

NovintiX is seeking a talented Manufacturing Engineer to join our team in Cork, working with a premier medical device manufacturer. This position offers the chance to play a key role in advancing innovative healthcare solutions. The selected candidate will oversee daily operations related to projects, products, and equipment, ensuring production targets are met. You will also contribute to process enhancements, collaborate with suppliers and R&D teams, and support new material and product introduction initiatives.

Key Responsibilities

• Evaluate and interpret specifications for processes, products, materials, or equipment to ensure optimal performance.
• Under general direction, collect and analyze operational, test, and experimental data to define benchmarks for new or updated products and processes.
• Review and interpret test outcomes, providing actionable insights to resolve technical challenges.
• Diagnose and resolve issues in new products or processes, partnering closely with product development teams.
• Collaborate with cross-functional groups to address production and engineering challenges.
• Perform hands-on troubleshooting of equipment and coordinate solutions with technical teams.
• Drive initiatives for process optimization, layout improvements, and enhanced operational efficiency.
• Support technicians, operators, and cross-disciplinary teams to achieve project and business objectives.
• Participate in the introduction of new products, contributing technical expertise from concept through implementation.
• Utilize Lean methodologies and root cause analysis tools to identify and address process issues.
• Develop and maintain technical documentation, including process and quality validation protocols.
• Apply knowledge of process mapping, risk assessment, and validation strategies.
• Foster a culture of continuous improvement and best practice adoption through active team engagement.
• Ensure compliance with health, safety, and environmental regulations in all engineering activities.
• Train and mentor team members, promoting knowledge sharing and technical excellence.
• Prioritize product quality and safety, adhering to all relevant industry standards and regulatory requirements.

Qualifications & Skills

• Bachelors or Master's Degree in Engineering (mechanical, Manufacturing, Biomedical, etc.,) or a related technical field.
• Proven experience in a manufacturing or process engineering role, preferably within the medical device sector.
• Strong analytical and problem-solving abilities.
• Hands-on experience with process improvement methodologies (e.g., Lean, Six Sigma).
• Excellent communication and teamwork skills, with the ability to work effectively across functions.
• Familiarity with regulatory standards and quality systems in the medical device industry.
• Demonstrated ability to manage multiple priorities and deliver results in a fast-paced environment.

Work Flexibility: Onsite

Shift - This role is for the Weekend shift. Working hours are 7am - 7pm, Friday, Saturday and Sunday.

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 initially a 12 month fixed term contract based in our Model Farm Road location

Travel Percentage: None

Additional Locations: N/A

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing – whatever your ambitions.

Purpose Statement

To design, implement, and optimize automated manufacturing systems and processes that enhance operational efficiency, product quality, and compliance with business goals.

Key Responsibilities

• Develop and deploy automation solutions to improve manufacturing throughput, quality, and cost-effectiveness.
• Lead troubleshooting and root cause analysis of automated equipment and systems.
• Collaborate with cross-functional teams to identify automation opportunities and implement scalable solutions.
• Monitor line performance and use data analytics to drive continuous improvement in automated processes.
• Create and maintain documentation including system specifications, validation protocols, and work instructions aligned with GMP standards.
• Support and lead initiatives under the Continuous Improvement Program (CIP) with a focus on automation.
• Manage the transfer and integration of automated processes from R&D or other manufacturing sites.
• Participate in phase reviews for new product introductions with a focus on automation readiness.
• Provide technical mentorship to Process Technicians and junior Engineers in automation technologies.
• Plan and execute automation-related projects including budgeting, specification, qualification, and handover.
• Ensure compliance with Equipment and Automated Systems (E&AS) procedures for new and existing automation assets.
• Monitor and report performance metrics related to automation systems and proactively resolve issues.
• Liaise with internal and external stakeholders to support automation goals and business targets.
• Ensure adherence to Environment Health and Safety (EHS) standards in all automation activities.
• Collaborate with Supplier Quality Engineers to manage risks associated with automated material handling and processing

Quality System Requirements

In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.

For those individuals that supervise others, the following statements are applicable:

• Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the BSC Quality Policy.
• Establishes and promotes a work environment that supports the Quality Policy and Quality System.

Job Scope and Leveling Guidelines

Knowledge

A developing professional. Working knowledge and application of business and technical concepts, procedures and practices. General knowledge of industry practices, techniques, and standards. General understanding of business unit/group function. Exercises judgment when interpreting company policies and procedures to resolve a variety of issues.

Problem Solving

Develops solutions to a variety of problems of moderate scope and complexity where analysis of situations or data requires a review of identifiable factors. Exercises judgment to determine appropriate action. Has knowledge of alternatives and an understanding of their impact on the business or technological environment.

Planning and Organization

Plans, organizes, and prioritizes own daily work routine to meet established schedule.

Discretion/Latitude; Supervision Received; Decision Making

Works under general direction regarding the progress of projects and special assignments. May seek guidance in resolving problems, interpretating established policies, procedures and practices. Work is reviewed for soundness of judgment.

Business Relationships and Project Management

Cultivates a wide range of internal business relationships and begins to develop an external network of resources to facilitate completion of tasks. May lead a project team of small to moderate scope. Influence exerted at peer level and occasionally at first levels of management.

Impact

Contributes to the completion of departmental projects and goals. Errors in judgment, poor recommendations, or failure to achieve results would normally require a moderate expenditure of resources to rectify.

Liaison

Engages with internal company and external contacts. Represents organization on specific projects. Uses diplomacy and tact in interactions and problem solving.

Mentoring

Provides guidance to less experienced staff.

Requisition ID:

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.

So, choosing a career with Boston Scientific (NYSE: BSX) isn't just business, it's personal. And if you're a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you