8 Surgical Equipment jobs in Ireland

Occupational Health Nurse Qualified Occ Health Nurse Location: Galway Permanent Full Time Position Monday Friday On site only role Excellent Benefits Connaught Salary euro An established multinational medical device manufacturing company in Galway is currently recruiting a qualified Occupational Health Nurse to work on site in Galway. We offer a favourable package and working environment with a strong focus on development. Requirements: A recognised qualification in Occupational Health is essential for this role. Registered General Nurse with a valid NMBI registration Excellent communication skills with strong interpersonal, empathy and listening skills. Strong organisational and planning skills including time management with proven track record of prioritizing key tasks and delivery to a high professional standard. Strong team member with proven ability to establish and maintain effective working people relationships. Minimum of 2 years plus of experience in occupational health nursing. Occupational Health Nurse duties: * Case management triage for all HR referrals, with OHN initial assessment and booking into OP diary. OP visits half day per week. * Health surveillance 2 yearly recalls * Vision assessment annually * Work related injury follow up * Flu clinics annually If you are a highly motivated and experienced OH Nurse looking for a new challenge, we encourage you to apply for this exciting opportunity. We would be delighted to hear from you. This is an exciting opportunity to get your foot in the door of an excellent reputable organisation. Salary is excellent & negotiable for the right candidate, excellent benefits, flexible hours & much more! 5 days per week on-site Monday to Friday generally 8am - 4:30pm or 8.30am 5pm. IND1 For more information call Maria O' Dwyer today on or for more information on this client & a confidential chat please call Maria on or email Maria on Skills: Occ Health Nurse Occupational Health Nurse NMBI Nurse #occhealthnurse#occupationalhealthnurse#nmbi#Galway Skills: Occupational Health Nurse Occ Health Nurse Occ Health Nurse Medical Device Galway Benefits: excellent

I am keen to speak with R&D Engineers who are looking to further develop their career in the Design and Development of Medical Device Products. Working on R&D Projects at my clients state of the art Medical Device Design Facility, you will work in cross-functional teams based in Ireland and liaise with other R&D Teams Internationally. I currently have a range of roles from Engineer Level (€65k) to Senior Engineer Level (€5k+). As well as offering competitive packages ( my client has an award-winning culture and at ISS Ltd (Recruitment Agency) we are offering a Signing Bonus ( APPLY TODAY R&D Engineer / Research & Development / Improve Current Product Design / NPD / Design Controls / Material Science Engineer / Hydrophilic Coated Products / Polymer Science / Medical Device / Mayo / Ireland Job Title: R&D Engineer Location: Co. Mayo Package: Full Time / Permanent k+ Basic Annual Bonus (7.5% - 10%) Health Insurance (VHI) Pension Parking Canteen Paid Annual Leave Signing Bonus ( Role: The R&D Engineer is expected to help drive the development and integration of new materials, processes or technologies into new products and processes. You will have a good understanding of medical device design controls, be capable of participating in cross-functional teams and interfacing with colleagues at all levels within the organization while effectively delivering solutions which benefit our customers. Duties: Providing technical support to NPD, Global Marketing, Engineering and Manufacturing Leading or supporting project teams to select and demonstrate the feasibility of alternative materials, processes or technologies for new and existing products Preparation of technical documentation in accordance with regulatory and design control requirements and with the company's development processes Working with cross functional partners to gather stakeholders input and develop plans to ensure requirements are assessed and met by proposed technical solutions Developing protocols and experimental test plans and managing the product build, transportation and storage as well as the execution of testing Conducting statistical analysis of data and developing detailed reports documenting results, conclusions and recommendations Representing the Research & Development function on cross-functional teams throughout the New Product Commercialization process Company: An established Multinational with Manufacturing and R&D facilities on-site in Ireland. Manufacturing a range of disposable Medical Device Products used across the Healthcare Sector. Experience: Third Level Degree (Hon) in Materials / Polymer Science / Mechanical / Biomedical Engineering 5 Years commercial experience in a R&D role (Medical Device Industry) An understanding of hydrophilic coatings and related technologies Skills Matrix: Attention to detail and good understanding of design controls and associated documentation A demonstrated track-record of being part of successful cross-functional technical teams Innovative / Creative Thinker; must have a demonstrated ability to conduct exploration of subject areas for novel concepts and approaches Demonstrated analytical problem-solving abilities Demonstrated ability to manage projects including directing the work of others Good team working skills and a high level of enthusiasm and motivation Good working knowledge of medical device quality & regulatory systems and medical device directives Experience of hydrophilic coating technologies, materials science and surface chemistry If you would like to be considered for this opportunity, follow the links below and send me your CV. Other R&D Roles @ ISS Ltd: Snr R&D Team Lead / k+ R&D Project Manager / k+ R&D Lead Packaging Engineer / k+ Key Words: R&D Engineer / Research & Development / Improve Current Product Design / NPD / Design Controls / Material Science Engineer / Hydrophilic Coated Products / Polymer Science / Medical Device / Mayo / Ireland Independent Search Solutions (ISS Ltd) is as the name suggests an Independent Recruitment Agency that aims to treat all its applicants with the up-most respect and in a professional manner. With a Company code of practice in place, you can be assured that your details will not be shown to any of ISS Ltds clients without your consent. Skills: Medical Device R&D Engineer Research And Development Material Science Engineer Hydrophilic Coating Technology Polymer Science R&D Mechanical Engineering Benefits: Annual Bonus / 13th Cheque Group Life Assurance Meal Allowance / Canteen Medical Aid / Health Care Paid Holidays Pension Fund Performance Bonus

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
The Quality Manager is responsible for leading the sustainment, improvement, and globalization of the AbbVie quality management system in support of AbbVie medical devices and combination products. This role serves as the Person Responsible for Regulatory Compliance for the EU Authorized Representative under EU MDR 2017/745, providing compliance subject matter expertise to internal business partners, demonstrating AbbVie quality management system compliance to external regulators, and leading continuous process improvement & globalization initiatives with other cross-functional AbbVie team members.
Ideally, this person will be based near one of our sites that manufacture medical devices in Ireland, either in Sligo or Westport.
Responsibilities:
+ Serve as the Person Responsible for Regulatory Compliance (PRRC) for the EU Authorized Representative, fulfilling all in-country obligations under EU MDR 2017/745.
+ Host external audits in the EU region, demonstrating AbbVie quality management system compliance to external regulators for ISO 13485 and other country-specific device audits.
+ Conduct internal audits to assess the compliance of AbbVie quality management system in accordance with ISO 13485 and other country-specific device regulations under MDSAP.
+ Lead root cause investigation and corrective action planning in response to external and internal audit observations, in collaboration with departmental process owners and subject matter experts.
+ Maintain expertise in both current and emerging regulations and standards impacting AbbVie medical device and combination products.
+ Perform regulatory compliance assessments of high complexity to support decision-making in critical business decisions, including Market Actions.
+ Analyze and interpret quality system performance metrics, presenting to Top Management as part of Management Reviews.
+ Program-manage initiatives intended to improve and globalize the AbbVie quality management system.
Qualifications
+ Bachelor's degree, preferably in engineering, physical science (e.g., Chemistry), life science (e.g., Microbiology or Biology), or pharmacy and a minimum of 7 years of industry experience in a GXP regulated environment.
+ ISO 13485 Lead Auditor certification by a professional body is preferred. Additional accreditation by a professional body is desirable; examples include American Society of Quality (ASQ) Certified Manager of Quality & Operational Excellence (CMQ-OE), Six Sigma Black Belt Certification, or Project Management Professional (PMP) Certification.
+ Operates with a high degree of autonomy and accountability, making independent quality and compliance decisions timely and demonstrating the ability to manage multiple commitments while delivering on-time. The role also demonstrates an enterprise mindset, being able to influence without direct authority and apply past learnings to novel situations.
This is a hybrid role with 3 days on site, 2 days remote.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community? Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
The Quality Manager is responsible for leading the sustainment, improvement, and globalization of the AbbVie quality management system in support of AbbVie medical devices and combination products. This role serves as the Person Responsible for Regulatory Compliance for the EU Authorized Representative under EU MDR 2017/745, providing compliance subject matter expertise to internal business partners, demonstrating AbbVie quality management system compliance to external regulators, and leading continuous process improvement & globalization initiatives with other cross-functional AbbVie team members.
Ideally, this person will be based near one of our sites that manufacture medical devices in Ireland, either in Sligo or Westport.
Responsibilities:
+ Serve as the Person Responsible for Regulatory Compliance (PRRC) for the EU Authorized Representative, fulfilling all in-country obligations under EU MDR 2017/745.
+ Host external audits in the EU region, demonstrating AbbVie quality management system compliance to external regulators for ISO 13485 and other country-specific device audits.
+ Conduct internal audits to assess the compliance of AbbVie quality management system in accordance with ISO 13485 and other country-specific device regulations under MDSAP.
+ Lead root cause investigation and corrective action planning in response to external and internal audit observations, in collaboration with departmental process owners and subject matter experts.
+ Maintain expertise in both current and emerging regulations and standards impacting AbbVie medical device and combination products.
+ Perform regulatory compliance assessments of high complexity to support decision-making in critical business decisions, including Market Actions.
+ Analyze and interpret quality system performance metrics, presenting to Top Management as part of Management Reviews.
+ Program-manage initiatives intended to improve and globalize the AbbVie quality management system.
Qualifications
+ Bachelor's degree, preferably in engineering, physical science (e.g., Chemistry), life science (e.g., Microbiology or Biology), or pharmacy and a minimum of 7 years of industry experience in a GXP regulated environment.
+ ISO 13485 Lead Auditor certification by a professional body is preferred. Additional accreditation by a professional body is desirable; examples include American Society of Quality (ASQ) Certified Manager of Quality & Operational Excellence (CMQ-OE), Six Sigma Black Belt Certification, or Project Management Professional (PMP) Certification.
+ Operates with a high degree of autonomy and accountability, making independent quality and compliance decisions timely and demonstrating the ability to manage multiple commitments while delivering on-time. The role also demonstrates an enterprise mindset, being able to influence without direct authority and apply past learnings to novel situations.
This is a hybrid role with 3 days on site, 2 days remote.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community? Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
The Quality Manager is responsible for leading the sustainment, improvement, and globalization of the AbbVie quality management system in support of AbbVie medical devices and combination products. This role serves as the Person Responsible for Regulatory Compliance for the EU Authorized Representative under EU MDR 2017/745, providing compliance subject matter expertise to internal business partners, demonstrating AbbVie quality management system compliance to external regulators, and leading continuous process improvement & globalization initiatives with other cross-functional AbbVie team members.
Ideally, this person will be based near one of our sites that manufacture medical devices in Ireland, either in Sligo or Westport, otherwise in one of our other Ireland sites.
Responsibilities:
+ Serve as the Person Responsible for Regulatory Compliance (PRRC) for the EU Authorized Representative, fulfilling all in-country obligations under EU MDR 2017/745.
+ Host external audits in the EU region, demonstrating AbbVie quality management system compliance to external regulators for ISO 13485 and other country-specific device audits.
+ Conduct internal audits to assess the compliance of AbbVie quality management system in accordance with ISO 13485 and other country-specific device regulations under MDSAP.
+ Lead root cause investigation and corrective action planning in response to external and internal audit observations, in collaboration with departmental process owners and subject matter experts.
+ Maintain expertise in both current and emerging regulations and standards impacting AbbVie medical device and combination products.
+ Perform regulatory compliance assessments of high complexity to support decision-making in critical business decisions, including Market Actions.
+ Analyze and interpret quality system performance metrics, presenting to Top Management as part of Management Reviews.
+ Program-manage initiatives intended to improve and globalize the AbbVie quality management system.
Qualifications
+ Bachelor's degree, preferably in engineering, physical science (e.g., Chemistry), life science (e.g., Microbiology or Biology), or pharmacy and a minimum of 7 years of industry experience in a GXP regulated environment.
+ ISO 13485 Lead Auditor certification by a professional body is preferred. Additional accreditation by a professional body is desirable; examples include American Society of Quality (ASQ) Certified Manager of Quality & Operational Excellence (CMQ-OE), Six Sigma Black Belt Certification, or Project Management Professional (PMP) Certification.
+ Operates with a high degree of autonomy and accountability, making independent quality and compliance decisions timely and demonstrating the ability to manage multiple commitments while delivering on-time. The role also demonstrates an enterprise mindset, being able to influence without direct authority and apply past learnings to novel situations.
This is a hybrid role with 3 days on site, 2 days remote.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community? Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

Location: County Tipperary (On-site)
Contract: 12-Month Fixed Term (with potential for extension)

Our client, a well-established engineering firm, is seeking a Tooling & Equipment Design Engineer to support the development of custom tooling and mechanical systems for implantable medical devices. The role is based on-site at a world-class manufacturing facility in County Tipperary. This is a hands-on, technically challenging role ideal for an experienced mechanical engineer who enjoys precision design, collaboration, and seeing their work make a real-world impact.

Responsibilities include but are not limited to:

• Design and develop mechanical tooling, fixtures, and assembly equipment to support advanced medical device manufacturing.

• Create detailed 3D models and engineering drawings using CAD (preferably SolidWorks).

• Collaborate with manufacturing, quality, and product development teams to ensure seamless integration of new equipment and processes.

• Participate in design reviews, technical problem-solving, and continuous improvement initiatives.

• Liaise with external vendors, suppliers, and equipment manufacturers to ensure quality and timely delivery of components.

• Support the validation and qualification of new equipment and processes as required.

• 3+ years of mechanical design experience, ideally in tooling, fixtures, or automation within a medical device or regulated manufacturing environment.

• Strong proficiency in CAD (SolidWorks preferred).

• Solid understanding of mechanical engineering principles, materials, and production techniques.

• Proven ability to deliver detailed and accurate mechanical designs within project timelines.

• Excellent problem-solving skills and attention to detail.

• Strong communication and teamwork skills.

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