7 Medtronic jobs in Ireland

Maintenance Technician - Manufacturing Location: Cork Schedule: Monday to Friday (On-call rotation included) An exciting opportunity has opened for a Maintenance Technician to join a leading high-precision manufacturing facility. This role is ideal for a hands-on technician with experience in preventative and reactive maintenance, troubleshooting mechanical and electrical systems, and optimising equipment performance in a high-tech production environment. Key Responsibilities: Perform preventative and reactive maintenance on production equipment, including CNC machines, robotics, pneumatics, and hydraulics. Troubleshoot electrical and mechanical issues to minimise downtime and improve efficiency. Work with automation systems, PLCs, and control panels to ensure seamless production. Support continuous improvement initiatives and TPM (Total Productive Maintenance) programs. Manage spare parts inventory, vendor coordination, and maintenance planning. Participate in on-call rotation and respond to urgent maintenance requests. Requirements: Trade qualification in mechanical, electrical, or a related discipline. Experience in a manufacturing or high-precision production environment. Strong knowledge of CNC machines, automation systems, pneumatics, and hydraulics. Hands-on experience with fault diagnosis, repairs, and preventative maintenance. Familiarity with CMMS systems (SAP, Maximo, etc.) for maintenance tracking. Ability to work independently and as part of a team in a fast-paced setting. What's on Offer: Private medical insurance, company pension, and other benefits. Funded training programs (e.g., ABB, Six Sigma) to develop technical skills. A collaborative and high-tech work environment with career growth opportunities. Interested? Apply now or reach out for more details. Skills: Maintenance Electrical Mechanical

Senior Manufacturing QA Engineer - Medical Devices Location: Galway / Hybrid | Type: Permanent | Sector: Medical Devices | Salary: Competitive An innovative and fast-scaling medical device company is seeking a Senior Manufacturing QA Engineer to support commercial manufacturing of a cutting-edge connected health solution for chronic wound care. This role is ideal for a quality professional with experience in manufacturing, supplier oversight, and regulatory compliance. You'll work across internal operations and contract manufacturing to ensure product quality, compliance with ISO 13485 / FDA 21 CFR 820, and readiness for regulatory inspections. Key Responsibilities: Oversee quality for electronics/system-level manufacturing with CMs Lead investigations and CAPA for non-conformances Support IQ/OQ/PQ validations and documentation reviews Monitor supplier quality and contribute to audit preparedness Collaborate on regulatory submissions and inspection readiness Requirements: Degree in Engineering, Quality, or a related discipline 3-7 years in QA or manufacturing quality within a regulated industry Strong knowledge of ISO 13485, FDA QSR, and process validation Experience supporting regulatory audits or working with Regulatory Affairs teams Advantageous: Contract manufacturing experience, CQE, Six Sigma, or auditing certifications For more info, contact Seamus at Reperio or apply through the link Reperio Human Capital acts as an Employment Agency and an Employment Business. Skills: QA QMS RA Medical Devices Galway

Location: Galway (On-site)
Industry: Medical Device / Start-up
Our client, a dynamic and fast-paced medical device start-up based in Galway, is seeking a Quality Engineer I to join their growing team. The company is focused on developing innovative, patient-centric technologies to improve quality of life and is advancing rapidly through the product development lifecycle toward global market launch.

This role offers a unique opportunity for a motivated and hands-on quality professional to apply their engineering knowledge across multiple areas of a developing Quality Management System. The ideal candidate will enjoy working in a cross-functional, start-up environment and contributing directly to impactful product development.

Responsibilities include but are not limited to the following:

• Apply quality engineering expertise across the Quality Management System (QMS).

• Support certification and maintenance of compliance to ISO 13485 and 21 CFR Part 820.

• Assist with design assurance activities, including design controls, verification, and validation.

• Support development and validation of test methods and computer system assurance programs.

• Participate in risk management and usability engineering activities.

• Maintain document control through QT9 eQMS and perform related administrative tasks.

• Contribute to the CAPA and non-conformance (NC) investigation and resolution process.

• Assist in internal and external audits and implement corrective actions as needed.

• Support updates and gap assessments for applicable regulatory standards and guidance.

• Participate in supplier quality management, vendor evaluation, and AVL maintenance.

• Collaborate cross-functionally to uphold quality objectives and continuous improvement.

• Perform additional quality-related duties to support business goals and KPIs.

• Bachelor’s degree in engineering, science, or related field (or equivalent).

• Minimum of 2 years' experience in a medical device or supplier environment.

• Familiarity with ISO 13485, FDA QSR (21 CFR Part 820), and GMP requirements.

• Experience in both FDA and European regulatory environments is preferred.

• Strong initiative, problem-solving, and follow-through in executing responsibilities.

• Understanding of risk management methodologies (ISO 14971).

• Experience with sterilization (EtO/Gamma), biocompatibility, and transportation testing is a plus.

• Prior involvement in audits or inspections is an advantage.

• Proficiency in MS Office and familiarity with electronic QMS tools.

Immediate interviews available for suitable candidates.

Note: By applying for this position, you may also be considered by Pale Blue Dot® Recruitment for other future vacancies

 Pale Blue Dot® Recruitment

The Experts in STEM Workforce Solutions

Medical Sales Specialist Acute Care Capital Equipment Location: Flexible - Limerick, Cork, Tipperary, Waterford etc Home office Supported The Company A Global, FTSE listed PLC with revenues totalling €1bn+, their healthcare division are one of Irelands largest Life Sciences companies, employing over 3000 people both here & overseas. Exclusively representing some of the biggest global bands in Science & Healthcare, they offer systems, products & services to the hospital, pharmaceutical & research sectors supplying diagnostics, medical devices, orthopaedic reconstruction, hospital equipment, laboratory instrumentation, critical care equipment plus associated services & support. They wish to appoint a Territory Manager to their Acute Care Capital Equipment division. The Role Managing an already well-established territory and exclusively representing some major global brands across theatre equipment, infusion, patent monitoring, imagining & infection control, the role will involve working with surgical consultants, nursing, theatre managers and procurement across both public & private hospitals in the Munster region. Along with responsibility for delivering revenue objectives for the area, the role will also involve product support & training in order to deliver best patient outcomes. Keen to speak to industry experienced individuals, applicants from nursing & theatre support staff seeking a commercial career also welcomed. Full product training provided. The Reward Great opportunity to build a longer-term career with one of Ireland's larger Life Science companies, managing a profitable territory with procurement contracts in place. With several sales teams operating across their various divisions, there are career development opportunities available for anyone who makes an impact. On offer will be a comprehensive package including an attractive base salary, commission plan, company car, lunch allowance, pension etc. For a confidential discussion contact Geoff Collins Pinnacle specialise in Life Science led sales roles, to view similar positions go to our website and view Sectors section. Benefits: Work From Home

**FIXED TERM CONTRACT**
**Abbott in Ireland**
Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. We have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Kilkenny, Longford, and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations, and shared services in Dublin and Galway. We have been operating in Ireland since 1946.
**Abbott Nutrition**
Our nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow, to keeping adult bodies strong and active. Millions of people around the world count on our leading brands - including Similac®, PediaSure®, Pedialyte®, Ensure®, Glucerna® and ZonePerfect® - to help get the nutrients they need to live their healthiest life.
**PURPOSE OF THE JOB**
As a Medical Safety & Surveillance (MSS) Global Medical Device Manager, the candidate will use his/her in-depth understanding of medical devices to ensure compliance with regulatory requirements for Abbott Nutrition medical devices. The MSS Global Medical Device Manager will have responsibility for generating documentation that supports Abbott Nutrition's global medical device registration and on-going compliance with EUMDR. This may include development and implementation of global standardized operating procedures. The candidate may also lead the development/maintenance of local medical device vigilance systems (predominantly for UK and EU), ensuring compliance with local regulations. The candidate will have departmental, cross functional, and global influence, and will be considered a medical device subject matter expert within the company.
**MAJOR RESPONSIBILITIES**
+ Organizes, manages and maintains a highly compliant global medical device system for Abbott Nutrition.
+ Maintains awareness and ensures compliance with established and updated local and global medical device processes as well as local and global regulations and guidelines for medical device registration and post-market documentation.
+ Develops and implements training programs for individuals involved in medical device activities.
+ Monitors medical device system performance; tracks compliance metrics and reports to global MSS Leadership Team.
+ Ensures global/local medical device audit readiness; Supports medical device audits/inspections and leads activities related to corrective and preventative actions for any audit findings.
+ Actively contributes to activities related to the monitoring of safety profiles for Abbott Nutrition products registered as medical devices, such as signal detection, evaluation, and prioritization.
+ Reviews and provides input to product DFMEAs.
+ Assists local staff with drafting and implementation of Safety Data Exchange Agreements, if applicable.
+ Works cross-functionally with Regulatory Affairs and Quality Assurance functions to maintain current knowledge of regulatory safety reporting guidelines and implementing relevant guidelines into practices and procedures.
+ Assists in the preparation, review and submission of aggregate safety reports.
+ Accountable for strategic preparation of medical device regulatory submission documentation (i.e. CEP, CER, PSUR, PMCF etc) and on-time completion of these activities for the division.
**EDUCATION & COMPETENCIES**
+ Master's degree in related health science or equivalent skills, education, or experience.
+ RAC certification is a plus.
+ 5-7 years of experience and proficiency in medical device regulatory submissions to Notified Bodies under EUMDR / MedDEV and knowledge of Medical Device standards and guidelines (such as ISO, GSPR, and MDGC).
+ Solid understanding and working knowledge of medical device regulatory requirements and in the development and implementation of processes to maintain compliance.
+ Strong medical knowledge and understanding to support safety related activities; background/experience with nutrition/nutritional products is a plus.
+ Knowledge of Vigilance reporting regulations on a Global scale.
+ Minimum 3 years of experience in leading complex projects or programs; global/regional experience desirable.
+ Fluency in spoken/written English;
+ Computer proficient (Windows, Word, Excel); experience working in adverse event databases.
+ Excellent communication and interpersonal skills, both written and spoken.
+ Strong organizational skills with proven ability to prioritize and work on multiple tasks and projects.
+ Strong commitment to compliance with the relevant rules and procedures and to scientific quality and integrity.
+ High level of accountability and reliability.
+ Demonstrates ability to work productively as a team.
+ Ability to work in a fast paced, changing environment.
+ Ease of operating in high stress, big decision situations.
+ Continuous improvement mindset.
+ Ability to influence a team in a positive way in relation to performance, change, and culture.
+ Demonstrate broad knowledge of Abbott's business and how department processes/responsibilities interconnect.
+ Mastery of the inventory deployment planning process.
+ Exceptional problem-solving skills
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

Overview Who we are PM Group is an employee owned, international project delivery firm with a team of 3,700 + people. We are world leaders in the pharma, food, medtech and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organisations. We are focused on growing a sustainable business centred around our people, our clients and trade partners. We are looking for a Laboratory Test Technician to join our Medical Device Client's (GMP accredited manufacturer) to join the Research and Development (R&D) team. The successful candidate will have a strong technical knowledge base and experience in laboratory equipment, as well as experience with R&D testing and quality documentation. Responsibilities Daily Responsibilities Product testing to support program milestones. Participate in the generation of laboratory equipment operation, maintenance, calibration, and cleaning SOPs to ensure adherence to approved laboratory procedures. Using the laboratory with adherence to good laboratory practices (GLP) for product testing and good documentation practices (GDP) through planning, performing, monitoring, recording and reporting on product testing. Providing support in testing of root cause investigations on malfunctioning product. Ensuring that all work is carried out in compliance with the required regulatory standards, conforms to company policies and standard operating procedures (SOPs). Maintaining the laboratory and equipment to good safe working order and ensure readiness of the laboratory for internal/customer/regulatory inspections within the laboratory. Working as part of a dynamic team to collaboratively reach project targets and milestones. Maintaining appropriate recording and reporting systems on all engineering related matters (calibrations etc). Manage stock, including allocation and removal of products and waste. Qualifications Requirements The successful candidate will have a third level Engineer/Technical/Science qualification. You must have a clear understanding of R&D testing and have experience in a laboratory environment. The ideal candidate will have experience of working with mechanical testing equipment and tools. Ability to work autonomously and meet project deadlines with diligence. Good communications and time management skills. As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2025 business strategy. Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future. PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know. #LI-BW1