6 Medtronic jobs in Ireland

Medical Sales Executive Surgical Location Flexible Leinster./ Munster - Home office supported. The Company A Global, FTSE listed PLC with revenues in Ireland totalling €50m+, our client are one of Irelands largest Life Sciences companies. Offering products & services to the healthcare, research & pharma sectors, portfolio includes medical devices, hospital equipment, laboratory diagnostics, critical care capital equipment & consumables. Witnessing year-on-year double-digit growth across all market segments, they wish to appoint a Key

Manufacturing Engineer Waterford, County Waterford, Ireland Are you an engineer with a passion for building, problem-solving, and driving continuous improvement? This is an exciting opportunity to join a leading medical device manufacturer where you'll play a pivotal role in shaping processes that deliver safety, quality, and productivity. The Role As a key member of the engineering team, you will: Lead Engineering Change Notices (ECNs) and ensure smooth, timely implementation. Manage validation activities and oversee First Article Inspection (FAIR) reporting. Support New Product Introductions (NPI), acting as a project lead and working closely with customers and cross-functional teams. Provide CAD support, prepare technical drawings, and design jigs and fixtures. Define and optimise manufacturing and assembly processes, including external subcontract processes. Ensure compliance with SOPs and production system requirements. Drive continuous improvement initiatives to reduce waste and enhance efficiency. Stay current with new technologies and best practices within manufacturing. What We're Looking For Bachelor's degree in Engineering. 3-5 years' experience in medical devices or another highly regulated industry (pharma, aerospace, automotive). CAD experience (SolidWorks or equivalent). Familiarity with investigative techniques and statistical analysis tools (e.g., Minitab) desirable. Strong problem-solving mindset and a passion for process improvement. Why Join? You'll be part of a forward-thinking company at the forefront of advanced manufacturing, working on innovative projects that directly impact patient outcomes. This role offers excellent scope for career development, exposure to cutting-edge technologies, and the chance to make a real difference in a regulated, high-quality environment. Skills: Manufacturing Medical Devices Process

SSA are recruiting a LOTO Engineer for an on-site, local-hire role in Ireland, focused on Lockout/Tagout within the MedTech industry. This position is urgent and exclusive to candidates based in Ireland. Key Details Position: LOTO (Lockout/Tagout) Engineer Industry: Medical Devices / Safety Engineering / Compliance Location: Ireland (On-site; local candidates only) Type: Full-Time, Permanent Salary:€60,000 - €70,000& Package Full Job Description Our client is a respected MedTech manufacturer with operations across Ireland. They are now seeking a skilled LOTO Engineer to lead hazardous-energy control during equipment maintenance. This permanent, on-site position will be central to safeguarding staff, patients, equipment integrity, and regulatory compliance. Key Responsibilities Identify and document all energy sources (electrical, mechanical, pneumatic, hydraulic, etc.) Develop and implement detailed Lockout/Tagout procedures for medical and service equipment Deliver training for staff on LOTO protocols; conduct audits to verify adherence Oversee LOTO implementation during maintenance and servicing operations Maintain accurate records of LOTO activities, training sessions, and audits Ensure practices align with OSHA and EU safety and regulatory standards Investigate LOTO-related incidents or near-misses; drive corrective actions Qualifications & Experience Bachelors degree or diploma in Engineering, EHS, or related field 36 years experience managing LOTO programmes in MedTech or manufacturing Strong understanding of hazardous energy control best practice and standards Experience collaborating with maintenance teams and completing safety audits Excellent communication, documentation, and stakeholder engagement skills How to Apply Please reach out to Conor ODonnell at SSA Group for a confidential conversation at or Skills: EHS LOTO Engineering LOTO Safety Environmental Health & Safety Safety Medical Devices

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

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**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