30 Manufacturing jobs in Cork
Manufacturing Operator
Cork, Munster
Stryker
Posted 1 day ago
Job Viewed
Job Description
**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
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 initially a 12 month fixed term contract based in our Model Farm Road location**
#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.
This advertiser has chosen not to accept applicants from your region.
0
Engineer, Manufacturing
Carrigtwohill, Munster
Stryker
Posted 1 day ago
Job Viewed
Job Description
**Manufacturing Engineer**
**23 month fixed-term role**
**Springhill**
**Who we want:**
+ **Collaborative partners.** People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.
+ **Analytical problem solvers.** People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.
+ **Dedicated achievers.** People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
+ **Goal-oriented developers.** Keeping the customer and requirements squarely in focus, people who deliver safe and robust solutions.
**What you will do:**
+ Ensure quality of process and product as defined in 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 customer 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 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 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
**What you will need:**
+ Level 8 Degree in Engineering, Science or related discipline or equivalent technical experience.
+ 0- 2 years' experience in an Engineering role, ideally production, R&D, biomedical
+ Business understanding of operations and their impacts essential.
+ High level of PC and analytical skills required.
+ Flexibility essential.
+ Strong communication skills with both internal and external stakeholders.
+ Self-starter with demonstrated efficient work methods, analytical & problem solving skills and ability to handle multiple tasks in a fast paced environment.
+ The individual should enjoy working in a dynamic and results motivated team
+ environment.
+ Experience in an FDA regulated or regulated industry is beneficial.
+ Experience in a Six Sigma and Lean Manufacturing environment with proven improvement results is beneficial
+ Green or Black Belt 6 Sigma qualifications are beneficial
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.
**23 month fixed-term role**
**Springhill**
**Who we want:**
+ **Collaborative partners.** People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.
+ **Analytical problem solvers.** People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.
+ **Dedicated achievers.** People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
+ **Goal-oriented developers.** Keeping the customer and requirements squarely in focus, people who deliver safe and robust solutions.
**What you will do:**
+ Ensure quality of process and product as defined in 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 customer 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 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 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
**What you will need:**
+ Level 8 Degree in Engineering, Science or related discipline or equivalent technical experience.
+ 0- 2 years' experience in an Engineering role, ideally production, R&D, biomedical
+ Business understanding of operations and their impacts essential.
+ High level of PC and analytical skills required.
+ Flexibility essential.
+ Strong communication skills with both internal and external stakeholders.
+ Self-starter with demonstrated efficient work methods, analytical & problem solving skills and ability to handle multiple tasks in a fast paced environment.
+ The individual should enjoy working in a dynamic and results motivated team
+ environment.
+ Experience in an FDA regulated or regulated industry is beneficial.
+ Experience in a Six Sigma and Lean Manufacturing environment with proven improvement results is beneficial
+ Green or Black Belt 6 Sigma qualifications are beneficial
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
This advertiser has chosen not to accept applicants from your region.
1
Manufacturing Engineer
Cork, Munster
Stryker
Posted 5 days ago
Job Viewed
Job Description
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.
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.
This advertiser has chosen not to accept applicants from your region.
2
Engineer, Manufacturing
Cork, Munster
Stryker
Posted 5 days ago
Job Viewed
Job Description
**Project Engineer - Stryker Model Farm Road**
**(12-month FTC - with potential to extend)**
**Why engineering at Stryker?**
At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products. As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better. Here, you will work in a supportive culture with other incredibly talented and intelligent people, creating industry-leading medical technology products. You will also have growth opportunities as we have a culture that supports your personal and professional development.
Need another reason to apply? Check out these 8 reasons to join Stryker's engineering team: we are looking for:**
+ **Detail-oriented process improvers** . Critical thinkers who naturally see opportunities to develop and optimize work processes - finding ways to simplify, standardize and automate.
+ **Collaborative partners** . People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.
+ **Analytical problem solvers** . People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.
+ **Dedicated achievers.** People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
+ **Strategic thinkers.** People who enjoy analyzing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities.
**What you will do:**
+ Work with Engineering leaders to deliver business objectives through the application of engineering principles focused on quality, service, and cost.
+ Display proficiency in the use of process improvement and problem-solving manufacturing issues using Six-Sigma tools.
+ Providing technical leadership on all product and process issues and line performance monitoring to include performance management.
+ 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).
+ Process validation for products and processes; VP, IQ, OQ, PQ and associated documentation.
+ Conduct Gage R&R studies for products and new processes.
**What you will need:**
+ Level 8 degree in Engineering.
+ 0 to 2 years' experience in a manufacturing environment.
+ Demonstrable analytical and 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.
+ Confident and effective decision maker, with a proven leadership ability to negotiate and influence others.
+ Proven Project Management skills through the delivery of business-critical projects.
**About Stryker**
Stryker is one of the world's leading medical technology companies and, together with our customers, is driven to make healthcare better.
The company offers innovative products and services in Medical and Surgical, Neurotechnology, Orthopedics, and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 100 million patients annually.
More information is available at stryker.com ( role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
**(12-month FTC - with potential to extend)**
**Why engineering at Stryker?**
At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products. As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better. Here, you will work in a supportive culture with other incredibly talented and intelligent people, creating industry-leading medical technology products. You will also have growth opportunities as we have a culture that supports your personal and professional development.
Need another reason to apply? Check out these 8 reasons to join Stryker's engineering team: we are looking for:**
+ **Detail-oriented process improvers** . Critical thinkers who naturally see opportunities to develop and optimize work processes - finding ways to simplify, standardize and automate.
+ **Collaborative partners** . People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.
+ **Analytical problem solvers** . People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.
+ **Dedicated achievers.** People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
+ **Strategic thinkers.** People who enjoy analyzing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities.
**What you will do:**
+ Work with Engineering leaders to deliver business objectives through the application of engineering principles focused on quality, service, and cost.
+ Display proficiency in the use of process improvement and problem-solving manufacturing issues using Six-Sigma tools.
+ Providing technical leadership on all product and process issues and line performance monitoring to include performance management.
+ 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).
+ Process validation for products and processes; VP, IQ, OQ, PQ and associated documentation.
+ Conduct Gage R&R studies for products and new processes.
**What you will need:**
+ Level 8 degree in Engineering.
+ 0 to 2 years' experience in a manufacturing environment.
+ Demonstrable analytical and 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.
+ Confident and effective decision maker, with a proven leadership ability to negotiate and influence others.
+ Proven Project Management skills through the delivery of business-critical projects.
**About Stryker**
Stryker is one of the world's leading medical technology companies and, together with our customers, is driven to make healthcare better.
The company offers innovative products and services in Medical and Surgical, Neurotechnology, Orthopedics, and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 100 million patients annually.
More information is available at stryker.com ( role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
This advertiser has chosen not to accept applicants from your region.
3
Manufacturing Technician
Cork, Munster
Cregg Group
Posted today
Job Viewed
Job Description
Maintenance Technician 3 Day Week | Medical Device Manufacturer | Cork CREGG Recruitment is delighted to partner with a leading global medical device manufacturer in Cork, currently seeking a Maintenance Technician to join their dynamic team. This is a unique opportunity to work a 3-day week while enjoying an excellent shift premium giving you more work-life balance without sacrificing earnings. To apply, contact Mark at or . The Role Reporting to the Senior Maintenance Engineer, youll play a key part in ensuring equipment runs at peak performance. Using your electrical and mechanical expertise, youll keep high-tech manufacturing lines running smoothly, while maintaining the highest standards of safety, quality, and compliance. What Youll Be Doing Delivering planned preventative maintenance. Troubleshooting and repairing production equipment both planned and unplanned maintenance. Driving root cause analysis to implement lasting fixes and minimise downtime. Supporting Line Support teams to maximise machine uptime and output. Partnering with engineers and value streams on projects to eliminate recurring issues. Contributing to 5S + Safety and continuous improvement initiatives. Reporting effectively on maintenance activities and equipment status. Ensuring full compliance with GMP and FDA standards at all times. What You Bring A Level 6 Qualification (trade or relevant discipline). Strong electrical and electronic repair/diagnostic skills. Mechanical problem-solving expertise, with experience in pneumatics. Previous manufacturing experience (medical devices, pharma, or regulated industry an advantage). Knowledge of GMP; cleanroom experience beneficial but not essential. Proficiency with computers and maintenance systems (CMMS). A collaborative mindset, with excellent teamwork and communication skills. Why Join? ? Work just 3 days per week enjoy better work-life balance. ? Competitive pay with a premium shift allowance. ? Be part of a world-class medical device manufacturer with career growth opportunities. ? Work in a supportive, safety-focused, and innovation-driven environment. INDCRG Skills: maintenance electrical mechanical PLC trouble shooting fault finding
This advertiser has chosen not to accept applicants from your region.
4
Senior Engineer, Manufacturing
Cork, Munster
Stryker
Posted 5 days ago
Job Viewed
Job Description
**Senior Engineer, Manufacturing**
**Location: Tullagreen, Carrigtwohill.**
**Contract: 23 Month Contract**
**On-Site Position.**
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 prioritized approach in Value Centered 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.**
**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 pro-active identification and resolution of issues around any deficits in same.**
**Adherence to, and enforcement of all Environment 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**
**All other duties as assigned.**
**What you will need:**
**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.
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.
**Location: Tullagreen, Carrigtwohill.**
**Contract: 23 Month Contract**
**On-Site Position.**
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 prioritized approach in Value Centered 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.**
**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 pro-active identification and resolution of issues around any deficits in same.**
**Adherence to, and enforcement of all Environment 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**
**All other duties as assigned.**
**What you will need:**
**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.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
This advertiser has chosen not to accept applicants from your region.
5
Staff Engineer, Manufacturing
Cork, Munster
Stryker
Posted 5 days ago
Job Viewed
Job Description
**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.
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.
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.
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
This advertiser has chosen not to accept applicants from your region.
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6
Manufacturing Operator (Macroom)
Cork, Munster
Stryker
Posted 5 days ago
Job Viewed
Job Description
**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.
+ **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.
This advertiser has chosen not to accept applicants from your region.
7
Senior Manufacturing Engineer
Cork, Munster
CareerWise Recruitment
Posted today
Job Viewed
Job Description
A Senior / Principal 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 Honours 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
This advertiser has chosen not to accept applicants from your region.
8
Manufacturing Engineering Technician
Cork, Munster
Sanmina
Posted today
Job Viewed
Job Description
JOB TITLE: Manufacturing Engineering Technician DEPARTMENT: Engineering REPORTING TO: Lead Manufacturing Technician - Eng About Sanmina Fermoy Our Fermoy, Ireland, facility is FDA registered and certified to ISO ISO for the manufacture of high-quality PCBAs, subassemblies and complete devices up to and including Class III medical devices. Sanmina Fermoy's core specialization is manufacturing automation. We provide services for the entire product lifecycle from New Product Introduction (NPI), prototyping and process validation to complex volume manufacturing & test, shipping and repair. We create a state-of-the-art environment for manufacturing medical and other high-quality devices. The facility has a track record of 30 years of outstanding operational performance and customer service, backed by a highly experienced workforce. We hire people with a range of skills, experience, and backgrounds to fulfill roles in careers such as engineering, quality and manufacturing to name just a few. OBJECTIVES OF POSITION: The Manufacturing Engineering Technician ensures the smooth running of all Production Equipment in a High Volume Production Environment (SMT/Clean Room or Packaging). RESPONSIBILITIES: To maintain Production Equipment to maximise Quality, Output and Yield, in a High Volume Manufacturing Environment, while adhering to Good Manufacturing Practices (cGMP) Guidelines. Apply Root Cause and Problem Solving to troubleshoot Production Line Issues and optimise or repair Production Equipment quickly and efficiently. Execute Preventative Maintenance activities. Liaise with Cross-Functional Teams to communicate and manage operational issues. Complete all Documentation clearly and concisely in accordance with GDP (Good Documentation Practice) Guidelines. Participate in Continuous Improvement Projects to drive Process Improvements and Efficiency in pursuit of Operation Excellence. Assist with the commissioning of new Production Equipment. Maintain appropriate stock of spare parts. Cross-Train new Manufacturing Technicians as required. Flexibility to travel to support new Production Equipment Assessments/Site Visits/Training. Any ad hoc duties as required. Assure ongoing compliance with quality and industry regulatory requirements Ensure compliance with Health & Safety Legislation and Regulations. MEASUREMENTS: Measurements will be assessed against an agreed set of MBO's (Management Objectives) as detailed in the annual performance appraisal process. PERSONNEL SPECIFICATIONS ESSENTIAL: NFQ Level 6 Qualification in Technology, Mechanical / Automation Electrical, Electronics, Mechatronics or similar (Qualified Trades Personnel with Industrial Experience will also be considered.) A Technical skillset of a Mechanical nature A "Compliance Mindset" and a high level of attention to detail in following Procedure and completing Documentation. Good communication and influencing skills. Ability to work under own initiative. Availability to work Shift Patterns. DESIRABLE: Experience in High Volume Manufacturing. Experience in High Volume Automation/Robotics/PLCs Experience in a Regulated Manufacturing Environment. Experience in Pneumatics, Electrical, Hydraulics, Vision Systems, and Workshop Machining. Understanding of Process Capability. Understanding of MSA (Measurement System Analysis) & GR&R (Gauge Repeat & Reduction) Experience in FAT (Factory Acceptance Test), SAT (Site Acceptance Test), IOPQ (Installation, Operation, Performance Qualification). #Sanmina To Apply Please forward your CV via the APPLY Now button below.
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