23 Manufacturing jobs in Cork

**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**
#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.

**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**
#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.

Manufacturing Caretaker About Lee Strand Established in 1920, Lee Strand has grown from a local creamery on Church Street, Tralee, to a modern production plant located on a 10-acre site in Ballymullen since 1992. Over its storied 100 plus year history, the company has become deeply rooted in the local community and renowned for quality dairy products. Role Overview Were seeking a dedicated Manufacturing Caretaker to join the team. As caretaker of our manufacturing facility, you will be responsible for: Cleaning and maintaining of the offices and non-production areas. Ensure production site is always clean and tidy. Upkeep of yard and grass areas to a high standard. Carryout of repairs and site maintenance as required. Unloading and loading of deliveries for use in production. Ensure facilities comply with safety, hygiene, and operational standards. Work collaboratively with Production, Maintenance, and Quality Assurance teams. Carryout minor building repairs and projects. Experience & Skills Previous experience in caretaking / site maintenance roles is an advantage. Strong attention to safety and cleanliness. Effective communication and teamwork skills. Ability to work independently, prioritize tasks, and be solution-focused. Flexible schedule and willingness to cover out-of-hours duties when needed. Benefits Competitive salary, reflecting experience and qualifications. Access to company pension and on-site parking. Embrace a friendly, community-driven workforce, with regular company events. Contribute to a stable and iconic local employer, with scope for career growth. Qualifications Relevant technical or trade qualifications advantageous. Experience in production/facility hygiene and safe operations. Good record of attendance and punctuality. Forklift experience is advantageous. (training can be given to the right candidate)

Catalyx are seeking a Manufacturing Technician to join our team and work a 24/7 (4 cycle) shift on our customer site in Cork. As a Manufacturing Technician, you will require a working knowledge of manufacturing methods and procedures in our customer's pharmaceutical tableting production facility. Who We Are : Catalyx specializes in the science of operational processes. With a footprint across North America and Europe, the company carefully automates and services R&D, production, packaging, and delivery processes-globally-with a sophisticated blend of products, technologies, and lifecycle services. Catalyx is a trusted partner in delivering world-class lifecycle services to regulated and high-risk end markets. With a relentless commitment to innovation and excellence, we partner with life science and other highly regulated organisations, to empower them to enhance efficiency, and drive success. As part of this commitment, we are continuously developing our on-site teams to support the advancement of customer operations. Responsibilities: Work on routine assignments following established SOPS, Master Batch Record and cGMPs Perform moderately complex tasks associated with aseptic processing, dispensing, compaction, granulation, milling and coating Reporting any issue that needs to be resolved on line performance to Operations Lead Perform more complex troubleshooting unassisted Work on more complex manufacturing processes and assignments Clean (manually, and clean in place) and assembles equipment for production Perform detailed SAP (computerised software) and MES transactions in resolving inventory discrepancies Clean manufacturing area, including walls, ceilings, and floors Complete and maintain documentation related to assigned work, including log books, batch records etc Act as a point of contact for a compliance audit Operate drum coater and compression equipment or roller compactors Dispenses ingredients for batches Perform MBR manufacturing batch report updates Perform manual handling of product - loads and unloads tablets Deliver on agreed KPIs and metrics Other duties as requested Requirements: Three years relevant industrial experience in a cGMP manufacturing environment A relevant level 6 qualification is an advantage A technical/ engineering qualification or background is an advantage Excellent written and spoken communication skills with established interpersonal skills Proficiency in MS applications Demonstrates strong safety orientation with strict adherence to established safety practices and standards Detail orientated A can-do attitude towards customer delivery and performance Why Join Catalyx? At Catalyx we understand that our people are our greatest asset. For this reason and many others, we take care of them. The team in Catalyx benefits from a Total Rewards package. This includes great personal benefits and professional growth opportunities. Catalyx is an Equal Opportunity Employer. We are committed to creating a diverse and inclusive workplace where all individuals are valued, respected, and supported. We do not discriminate on the basis of race, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, veteran status, genetic information, or any other characteristic protected by applicable law. We encourage applications from all qualified candidates, regardless of background, and strive to create a welcoming environment for everyone. At Catalyx, we are committed to attracting the best global talent. We proudly support our international employees by offering assistance with Critical Skills Visa applications for eligible candidates. 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.

CREGG are hiring for a Maintenance Technician to join a large medical device manufacturer in Cork. This role is a Weekend Night Shift opportunity, working a3 day work week, Excellent shift premium provided. Apply to the role if you have previous Manufacturing experience, Trade qualified or hold a relevant level 6 Qualification. Contact Mark :or Reporting to the Senior Maintenance Engineer,your role is to provide electrical and mechanical maintenance supportto ensuring that equipment asset performance is maximised.A high maintenance standard is a must as is adherence to quality standards and safety. Key Responsibilities Maintain Planned Preventative Maintenance through CMMS System (BMRAM) Perform all maintenance of Production equipment, including planned and unplanned maintenance activities Carry out root cause analysis of all machine breakdown to allow corrective maintenance scheduled to be conducted. Provide knowledge to the Line Support team and work alongside to ensure maximum machine output is achieved The role involves helping the department achieve world-class equipment uptime by utilizing downtime and OEE (Overall Equipment Effectiveness) data. This is done by focusing on improving key metrics such as Mean Time to Repair (M.T.T.R.) and Mean Time Between Failures (M.T.B.F.). Collaborating with the Senior Maintenance Engineer and Value Streams to identify and implement projects that provide permanent solutions to recurring equipment downtime issues. Support and engage in the 5S + Safety program within Value Streams and Equipment Management as needed Promote and participate in the Maintenance departmentsContinuousImprovementProgram. Reporting of work status on a timely basis to the Senior Maintenance Engineer and Value Stream team leaders as appropriate. . Ensure all activities are carried out in accordance with the GMP requirements. Qualifications and Experience Minimum Level 6 Qualification Relevant working knowledge of an FDA regulated industry and GMP requirements. Experience working in a Cleanroom environment would be ideal but not required Strong electrical and electronic repair and diagnostic skills Strong mechanical systems problem solving & repair skills Experience in pneumatic fault finding and repair Demonstrate levels of theoretical knowledge with practical application. Good teamworking & communication skills Good computer skills. INDCRG Skills: maintenance electrical manufacturing medical devices technical sensors mechanical Benefits: Mobile phone Paid Holidays Canteen Gym Parking Staff discount Laptop

**Staff Engineer, Manufacturing - Stryker Neurovascular**
Initial 18 month FTC
As a Staff Engineer at Stryker, you'll be a technical trailblazer, providing expert leadership within our world-class facility. Leveraging your deep knowledge and experience, you'll tackle complex challenges and drive excellence in a highly specialized field. In this critical position, you'll lead all validation activities tied to the successful qualification of new injection moulding tools and process introductions-playing a key role in shaping the future of advanced medical manufacturing
**Key Areas of Responsibility**
+ Management of significant Engineering projects through PMO.
+ Write and execute process validation protocols and reports for new product introductions and re-validations due to process /material improvements utilising scientific / technical knowledge.
+ Must have a very good knowledge of injection mould tooling and design.
+ Provide Technical leadership from an engineering perspective.
+ Ownership of the plant metrics from an engineering perspective.
+ Technical and operational support to manufacturing operations.
+ Structured problem solving.
+ Continuously improve the performance of the process.
+ Provide support to Process Development / Advanced Operations on technology development and application within the manufacturing process.
+ Engage in the implementation of lean manufacture within manufacturing.
+ Interface with Materials Science, Design and Quality Assurance departments to provide customer with a quality product in a timely manner.
+ Support process development and cost reduction activities within the business units.
+ Communicate and participate in system and process troubleshooting with support team members and with external agents.
+ Provide leadership to other Manufacturing Engineers and or Technicians as required.
**Qualifications / Knowledge / Skills**
+ Level 8 Degree in Polymer or Mechanical Engineering or relevant discipline or equivalent technical experience is required.
+ Proven Project Management skills through the delivery of business critical projects.
+ Has minimum of 4 years experience in a manufacturing environment.
+ Strong communication and influencing skills with both internal and external agents.
+ Capable of providing technical leadership and, 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 strong analytical & problem solving skills, a process improvement orientation, and the ability to handle multiple tasks in a fast-paced environment
+ Excellent presentation and written / verbal communication skills
+ Demonstrable ability to work autonomously
+ A team player, with a flexible approach.
+ Technological expert, willing to source, investigate and implement technological and automation advances
+ Confident and effective decision maker, with a proven technical leadership ability to negotiate and influence others.
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 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.

Position Overview: The Manufacturing Validation Engineer will play a pivotal role in ensuring the validation and qualification of manufacturing equipment, systems, and processes in compliance with industry regulations and company standards in the medical device sector. This position combines technical expertise in manufacturing equipment, quality assurance processes, and project management abilities to oversee validation activities from initiation to completion. The role requires a blend of engineering, regulatory knowledge, and leadership skills to drive successful project delivery, including documentation, risk management, and effective collaboration across cross-functional teams. Key Responsibilities: Plan, execute, and manage validation protocols for manufacturing equipment, including IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) to ensure compliance with regulatory standards (FDA, ISO 13485, etc.). Lead the qualification of new and existing manufacturing equipment to ensure proper installation, performance, and consistent functionality. Ensure compliance with current Good Manufacturing Practices (cGMP) and other relevant standards throughout validation processes. Provide technical expertise on equipment, ensuring that systems and tools meet necessary specifications, performance criteria, and operational requirements. Lead root cause analysis and troubleshooting efforts when equipment issues arise during validation, identifying corrective and preventive actions (CAPA). Develop and review validation protocols, reports, and SOPs (Standard Operating Procedures) to ensure all activities are properly documented and compliant with regulatory requirements. Ensure the traceability and audit readiness of all validation activities, supporting internal audits and regulatory inspections. Support the creation and review of regulatory filings and submissions as required. Ensure proper documentation practices, maintaining the highest standards for data integrity and quality assurance throughout the validation process. Actively participate in continuous improvement efforts within the manufacturing area to optimize equipment performance, reduce waste, and enhance operational efficiency. Provide training and mentorship to junior engineers or technicians, guiding them through validation protocols, equipment troubleshooting, and best practices. Contribute to lessons learned meetings and share insights to improve future validation processes. Lead and manage validation projects from conception through to completion, ensuring all aspects of the project adhere to defined timelines, budgets, and quality standards. Develop project timelines and schedules, ensuring all milestones are met and delivering the required project updates to senior management and stakeholders. Coordinate cross-functional teams, including Engineering, Quality Assurance, Manufacturing, Regulatory Affairs, and Suppliers, to ensure the success of validation projects. Conduct risk assessments for validation activities and ensure mitigation plans are in place. Track and report on the progress of validation projects and proactively address any potential delays or risks to project timelines. Prepare and maintain validation documentation and ensure compliance with company standards, including change control documentation, project status reports, and validation summaries. Skills: Bachelors or Masters degree in Engineering, Mechanical Engineering, Industrial Engineering,or a related field. 5+ years of experience in manufacturing equipment validation, qualification, or a related engineering role within the medical device or pharmaceutical industry. At least 2 years of experience in project management, leading cross-functional teams and driving complex projects to completion in a regulated environment. Familiarity with regulatory standards such as FDA 21 CFR Part 820, ISO 13485, and cGMP. Expertise in validation practices (IQ/OQ/PQ) and associated documentation. Hands-on experience with manufacturing systems and equipment used in medical device production. Strong project management skills including the ability to create project timelines, track progress, and mitigate risks. PMP certification is a plus. Strong analytical and problem-solving skills, including root cause analysis and CAPA management. Ability to work collaboratively in a cross-functional team environment. Excellent communication skills, both written and verbal, with the ability to prepare detailed reports and present findings to management. Knowledge of industry-specific software, such as LIMS (Laboratory Information Management Systems), ERP (Enterprise Resource Planning), or Veeva Vault, is a plus. Familiarity with risk management principles (e.g., FMEA, Risk Assessment) and their application in equipment validation. Skills: validation manufacturing IQOQPQ Equipment qualification risk assessment verification manufacturing engineer

An exciting new vacancy for a Manufacturing Maintenance Supervisor is now open in our client's site in Blarney Work Your Magic with us! Ready to explore, break barriers, and discover more? We know youve got big plans so do we! Our colleagues across the globe love innovating with science and technology to enrich peoples lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. The Role The Manufacturing Maintenance Supervisor is responsible for directing and coordinating all technical and maintenance activities in support of production in a safe, cost-effective and environmentally friendly manner, assuring capacity and achieving plant performance metrics. Duties Include: Lead and drive continuous improvement initiatives identified through on-going assessment of equipment issues and reliability (based on gathered data and statistical analysis). Apply effective methods of preventative and corrective maintenance to ensure resource deployment is effective and efficient, including review / optimising of existing Preventative Maintenance Activities PM Optimisation. Responsible for the development and tracking of the departments KPIs in order to measure equipment and maintenance performance i.e. MTBF, MTTR, OEEs, schedule attainment, labour utilisation, work order backlog, PM / calibration completion rates, spare usage and costs control. Champion and lead asset condition management through the use of new technologies with a particular emphasis on non-intrusive testing, predictive maintenance and monitoring to maximise uptime and identify signs of early failure. Supervision of employees, allocating work, co-ordinate training and dealing with issues as arise up to counselling stage of disciplinary process. Ensure Attendance Management policy is adhered to. Lead and drive initiatives to mitigate re-occurring issues. Recruitment & Selection of all technicians for assigned department (s). Performance Management prepare, assess and conduct all 121s & appraisals including end year review, contract staff appraisals, etc. Providing a safe and injury free workplace for all employees. Ensure compliance with all applicable Environmental, Health and Safety legislation & adherence to Safety procedures & requirements. Partner with the Quality department to ensure compliance with Quality Standards. Foster culture of right first time (RFT) ensuring product quality Who You Are Minimum 8+ years experience in an Engineering / Technical / Maintenance Leadership role, preferably within the Life Science, Medical Device and / or Pharmaceutical Industry. Trades Qualified an advantage. Engineering (Level 7 or 8) in Mechanical or Electrical Engineering or recognised equivalent an advantage. Experience or Qualification in Reliability Engineering an advantage. Work Experience High level of energy, positivity and enthusiasm and the ability to motivate others. Demonstrated high performance history, proven ability to execute and get results. Excellent leadership, facilitation, and communication skills Strong project management experience Ability to influence within a matrix organisation with direct and indirect authority. Ability to work with employees at all levels of the organisation. Experience with planning and executing change within a high work paced environment. Keen ability to teach and coach. Preferable experience with SAP Next / PM system. Preferable experience with a Calibration System. Previous experience within an ATEX environment an advantage. Experience with Planned Preventative and Proactive Maintenance approaches. Excellent awareness and experience in relation to Quality and Environmental Health and Safety Skills The ability to work effectively within a team environment. Lead a high performing technical group. Keen to learn & take responsibility. Analytical with experience in Lean Six Sigma Methodologies Familiar with GMP requirements within a regulated industry. Effective verbal, written & interpersonal communication skills. Self-motivated. Strong organisational, time management and planning ability. Computer Literate Excel, Word, Powerpoint etc. Methodical Work Approach. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of our diverse team! #LI-DL2 Skills: Reliability Engineering Maintenance Supervision Preventative Maintenance Benefits: Pension Bonus Laya Healthcare