medical devices jobs

Near limerick, limerick
120Jobs Found

120 jobs found for medical devices jobs Near limerick, limerick

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Research & Development Engineer

Cook Group

Limerick
22 days ago
Limerick
22 days ago

Design, development and taking to market of medical devices for one or more Cook Medical Strategic Business Units.

 

 

Reporting to: Senior Research & Development Engineer/Research & Development Manager  

 

 

 

Find out more about Cook Medical here


  • Perform Duties of Research & Development Engineer including:
    • Design development, prototyping, test method design, design evaluation, design reviews, design specifications, design verification and validation, design protocols and reports, transfer to production activities in a timely effective manner.
    • Product testing and evaluation, completion of test reports to support design selection.
    • Preparation and presentation of design reviews.
    • Product and project risk analysis and risk management.
    • Work with Process Development Engineering to introduce/develop new equipment and production processes as required for any new manufacturing techniques.
    • Source new materials components and equipment.
    • Development of component specifications, inspection methods, bills of materials and manufacturing processes.
    • Introduction of new equipment, materials and technologies.

 

  • Work closely with Key Opinion Leaders (KOL’s), physicians and product managers to develop innovative medical devices to improve patient care.

 

 

  • Project lead for assigned research & development projects including technical and project management responsibly.
    • Manage and drive project tasks to ensure timely completion of project milestones.
    • Work closely with cross functional groups to achieve project and company goals.
    • Product performance evaluations.
    • Contribute to innovation and creativity within team through filing of disclosures and patents.
    • Hold regular project meetings and document minutes and actions.
    • Ensure project milestones are achieved to meet business metrics.

 

 

 

  • Compliance with Quality, Regulatory and company policies and systems.
  • Communications:
    • Regular communication to cross-functional teams, senior management and business unit leaders.
    • Project status communications and reporting.
  • Remain on the forefront of emerging industry practice

 

 

  • Educating oneself in the medical area for which the new devices are being developed in order to have an appreciation for what needs to be achieved with these products.
  • Support other cross functional groups to deliver company goals.#
  • Ensure that Cook’s Code of Conduct is considered in all business matters carried out on Cook’s behalf.

 


  • Third level degree in Mechanical, Biomedical, Design, Chemical Engineering or similar discipline.
  • 2 Years design experience medical device roles.
  • Project planning skills.
  • Execution of project in a timely effective manner.
  • Knowledge of anatomy and physiology.
  • Good mechanical design and understanding of engineering fundamentals with extensive medical device materials knowledge.
  • Manufacturing design and process understanding.
  • Good working knowledge of Solidworks and/or Pro Engineer CAD.
  • Strong technical writer.
  • Knowledge of medical device quality & regulatory systems and medical device directives (ISO13485 and FDA CFR 820), EU Medical Device Regulation 2017/745.
  • Team Player with ability to develop strong working relationships.
  • Strong communication and inter-personal skills.
  • Good problem solving skills.
  • Highly motivated individual, self-starter with a passion for excellence.
  • Must be able to work in a fast paced environment.
  • Willingness and availability to travel on company business.

 

 

 

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Senior Quality Engineer

Webrecruit Ireland

Limerick, Limerick
28 days ago
Limerick, Limerick
28 days ago

Senior Quality Engineer

Limerick, Co. Limerick

 

The Company

 

Fleming Medical is a market-leading pharmacy supplies company based in Limerick which has grown internationally by design innovation in consumer healthcare products.

 

They are now seeking a Senior Quality Engineer to join their team in Limerick.

 

The Benefits

 

- Competitive salary

- VHI cover

- 20 days’ holiday

- Join a successful regulated medical device and healthcare distribution business

 

This is the ideal role for a quality-focused professional with an excellent grasp of quality assurance and regulatory standards to advance their career with a growing and highly successful organisation.

 

You will have the chance to play a pivotal role in building the company’s operational excellence across a diversified product portfolio.

 

So, if you want to support the delivery of pioneering products that are helping healthcare professionals across the globe to save lives, our client wants to hear from you.

 

The Role

 

As the Senior Quality Engineer, you will be tasked with driving compliance and continuous improvement of the site quality management system to the required quality and regulatory standards.

 

Driving compliance with activities such as new product introduction, supplier quality, change control, complaints, NC & CAPA, you will also seek to drive improvements to meet KPIs.

 

Managing and controlling document with the QMS, you will seek to improve QMS documents and systems, co-ordinate internal audits and identify and implement operational improvement initiatives.

 

Additionally, you will:

 

- Drive Quality requirements related to New Product Introduction

- Continuously assess the regulatory impact on new product releases or product updates

- Maintain appropriate product records to demonstrate compliance

- Develop appropriate trending analysis and sampling plan reviews

- Prepare for and participate in external regulatory inspections

 

About You

 

To be considered as a Senior Quality Engineer, you will need:

 

- Good knowledge of quality assurance and regulatory standards

- Good technical writing skills and experience

- Good computer skills including knowledge of Microsoft, ERP and QMS database systems

- Good communication and interpersonal skills with the ability to communicate clearly and concisely in both spoken and written form

- Attention to detail and accuracy to deal effectively with literature and data reviews

- To be self-motivated, flexible, organised and a good team player with the ability to prioritise own work based on departmental and site requirements

 

A third level qualification in a related discipline would be beneficial to your application, as would experience working in a similar quality assurance related role in the Medical Device Industry.

 

Other organisations may call this role Quality Engineer, Manufacturing Compliance Engineer, QA Engineer, Quality Assurance Engineer, QMS Engineer, or Compliance Engineer.

 

Webrecruit Ireland and Fleming Medical are equal opportunities employers, value diversity and are strongly committed to providing equal employment opportunities for all employees and all applicants for employment. Equal opportunities are the only acceptable way to conduct business and we believe that the more inclusive our environments are, the better our work will be.

 

To apply for the role of Senior Quality Engineer, please apply via the button shown. This vacancy is being advertised by Webrecruit Ireland Ltd. The services advertised by Webrecruit Ireland Ltd are those of an Employment Agency.

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Senior Embedded Engineer (C++) - R&D Medical Devices - Limerick

ITSearch

Limerick, Limerick
7 days ago
Limerick, Limerick
7 days ago

Senior Embedded Engineer (C++) - R&D Medical Devices - Limerick

 

My client based in Limerick is a world leading firm in the area of wearable technology and medical devices and has engaged IT Search to speak to candidates regarding this challenging senior role that will work within R&D to create complex medical devices.

 

The role is to join an existing global team headquartered here as a Senior team member, mentoring more junior staff but bringing significant expertise to the R&D team in the areas of designing, testing and implementing embedded processes at all levels of the architecture. Working within compliance and regulatory guidelines, this role will allow the Senior Engineer to produce cutting edge technological solutions to the medical community.

 

This will be a hybrid onsite/remote role so candidates will need to be based within a commuting distance.

 

Candidates should have:

  • 5 to 10 years of commercial development experience using C++ post graduation, ideally within a pharmaceutical or highly regulated environment
  • Ideally Firmware development experience
  • Linux (embedded) ARM and Cortex skills and architectural knowledge
  • Exceptional communications skills, able to work with multiple areas of the business and various locations and have a track record of strong documentation

 

To learn more about the role, client and process, please forward your CV stating required salary and availability and we can arrange a discussion.

 

Please note, we can only accept applications from candidates eligible to work in the EU

 

 

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Regulatory Officer

Adecco Retail

Limerick, Limerick
6 days ago
Limerick, Limerick
€35k - €45k Per Year
6 days ago
€35k - €45k Per Year
Adecco have an amazing opportunity for a Regulatory Officer to join a leading Molecular Diagnostics company-based in Limerick City (East). In this role you will report into the Director of Quality & Regulatory and be responsible for preparing and maintaining technical files and utilising information from cross-functional teams
Roles & Responsibilities:
*Review documentation and participate in R&D Phase Reviews
*Aid in coordination of Risk Management activities and file preparation
*Aid in coordination of Post Market Surveillance / Vigilance Reporting
*Communicate specific regulatory requirements to cross functional teams
*Prepare Regulatory Reports for Management as required
Specific Skills Required:
*Qualification: BSc molecular biology or related discipline
*Good Knowledge & understanding of IVD Directive/Regulation or Medical Device Directive/Regulation
*Experience working in ISO 13485 and FDA regulated companies
*Ability to work on own initiative
*Good command of Microsoft Office
Desirable Criteria:
*PhD in molecular biology or related discipline
*Experience in preparation of medical device technical files and regulatory submissions
*Good problem-solving skills
Adecco Ireland is acting as an Employment Agency in relation to this vacancy.
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Warehouse Operative/ Relief Driver

FRS Recruitment

Limerick, Limerick
5 days ago
Limerick, Limerick
€27k - €35k Per Year
5 days ago
€27k - €35k Per Year

Warehouse Operative/ Relief Driver
Perm -Days (no Shift)
Our client, a well-established multinational expert in providing supply chain services to pharma and medical device companies is looking for a Warehouse Operative/ Relief Driver to join their growing organisation.
This job is offering a Full-time days only, permanent position, job security, competitive pay, interesting fast paced rewarding work supporting medical device and pharma companies, progression, future employability as the experience you gain here is highly desired.
This is an excellent company to work for and they have very low turnover of staff. This type of role in this company does not come up very often and they are offering a very competitive salary for the right person.
We have been assisting this client for many years with their recruitment needs. This company is continuing to grow and expand even during a global pandemic. This company is positioned very well in the market allowing it to go from strength to strength.
Duties for the successful Warehouse Operative/ Relief Driver
Facilitate all inward and outbound stock movements for the branch efficiently, following company procedures, and using IT systems where appropriate.
  • Pick and pack goods in an efficient, timely and safe manner.
  • Actively maintain and improve housekeeping throughout working hours ensuring that stored goods are kept tidily and in the correct place, using mechanical handling equipment where appropriate in accordance with company procedures.
  • Ensure that with all aspects of Health & Safety policies and procedures are complied with in all daily activities.
  • Contribute to the effective operation of the branch by supporting other staff in meeting Customer Service levels.
  • Continually review operating systems. Procedures and practices, recommending any changes to improve operational effectiveness and efficiency and to reduce costs.
  • Making Deliveries to client sites on an as needed basis in 7.5 tonne Rigid Vehicle

Requirements for the successful Warehouse Operative/ Relief Driver
  • Experience with ERP systems such as SAP
  • An in date counter balance forklift certificate
  • Full CPCs and Digital Tachograph card
  • In date C- License
  • Strong IT skills
  • Previous experience in a Warehouse/Supply Chain role
  • Strong communications skills
  • Good team player
  • Hardworking and reliable

How I can help:
I have placed many people with this client, I can help guide you through the process and give you hints and tips that will give you a competitive advantage over other applicants.
Interested?
To apply for this exciting new position here are your three options:
"This sounds like me" - Call now and let's talk through your experience. Ask for Richard O'Sullivan (Recruiter) on 086 1852327 between 9 am - 5pm.
"I think I'm right for this position, but I'm not sure I have enough experience" - Click "apply now" so I can read your profile and let you know.
"I'm interested but need to know more about what this job can offer me" - email with your CV and questions and we'll set up a call to talk.
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Lead Software Developer - Limerick

E-Frontiers

Limerick, Limerick
2 days ago
Limerick, Limerick
€80k - €80k Per Year
2 days ago
€80k - €80k Per Year

We are looking for a talented C#, .NET Developer to join our client's security team, based in Limerick.
Our client, a Product company in the Medical Industry, is on the lookout for a Lead Software Developer (C#) to join their Security team in their Limerick office.
* we can only accept applications from candidates currently based in Ireland with European passports, Stamp 4 or Spousal visas.*
The Opportunity:
  • Lead technical design reviews and code inspections. Provide clear, actionable feedback for project team members.
  • Develop and administer software engineering procedures and training for vulnerability scans and static code analysis.
  • Implement software security solutions and architect/design products in accordance with industry accepted standards for medical device security including encryption, disaster recovery, authentication, audit logging, hardening measures, patch management, vulnerability monitoring, and antivirus/antimalware requirements
  • Lead product security risk assessments, hazard analysis, and provide vulnerability remediation guidance and mentoring to product development software engineers both on and off-site.

Skills:
  • Minimum of 5 years of experience in software development, systems & architecture concepts and designs
  • Minimum of 5 years work experience with C#/.NET development
  • Minimum of 5 years work experience in product development
  • Minimum of 3 years work experience using secure coding practices.
  • BS degree in Computer Science, Computer Engineering, Electrical Engineering, or other related engineering field is required.

Nice to Have:
  • Candidate for or certification in InfoSec Security are a plus, e.g. CSSLP
  • Knowledge of Completing a track Trace and plan using a Security Requirements Traceability Matrix (SRTM) or similar tool with the goal of tracking: Security Requirements, Source of Requirement, Requirement Objective, Verification Method.
  • Work experience in network security along with knowledge of Windows networking fundamentals (IP protocol, firewalls etc.) strongly desired
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Software Technical Lead

FRS Recruitment

Limerick, Limerick
5 days ago
Limerick, Limerick
5 days ago

FRS are delighted to announce a new Software Technical Lead position with our long term client partner in Limerick. You will develop a high functioning team while adhering to the core values, practices, and vision of both the agile manifesto and the company..
You will have:
  • A strong understanding of software design/systems/architecture concepts and their application in a professional environment within a software team structure.
  • Understanding of different software development life cycle methodologies, primarily Agile.
  • Excellent written and oral communication and interpersonal skills are essential
  • Be a 'hands-on' technical lead contributing to the software development effort (specify, plan, design, develop, test and support software components)
  • Architect and design system software components for medical device platforms

Your experience:
  • BS degree in Computer Science, Computer Engineering, Electrical Engineering, Mathematics, Physics or other related engineering field with a minimum of 8 years of experience in software development
  • Minimum of 5 years of experience in C# and .NET Framework
  • Minimum of 5 years of experience with Microsoft SQL Server and Entity Framework
  • Minimum of 4 years of experience with ASP.NET MVC development
  • Minimum of 4 years of experience with WebAPI 2
  • Minimum of 4 years of experience with JavaScript, HTML, LESS/CSS and Node.js
  • Minimum of 3 years of experience with .NET Core
  • Minimum of 2 years of experience with Angular 2 or later
  • Experience with JavaScript frameworks such as Bootstrap, jQuery or Knockout.js
  • Experience with source controls systems such as TFS, Azure DevOps and Git
  • Demonstrable understanding of, and experience with SOA and RESTful architectures
  • xUnit and Moq

Please send a fully updated, detailed cv via reply for this exciting new role.
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Research & Development Engineer

Cook Group

Limerick
23 days ago
Limerick
23 days ago

Overview

Design, development and taking to market of medical devices for one or more Cook Medical Strategic Business Units.

 

 

Reporting to: Senior Research & Development Engineer/Research & Development Manager  

 

 

 

Find out more about Cook Medical here

Responsibilities

  • Perform Duties of Research & Development Engineer including:
    • Design development, prototyping, test method design, design evaluation, design reviews, design specifications, design verification and validation, design protocols and reports, transfer to production activities in a timely effective manner.
    • Product testing and evaluation, completion of test reports to support design selection.
    • Preparation and presentation of design reviews.
    • Product and project risk analysis and risk management.
    • Work with Process Development Engineering to introduce/develop new equipment and production processes as required for any new manufacturing techniques.
    • Source new materials components and equipment.
    • Development of component specifications, inspection methods, bills of materials and manufacturing processes.
    • Introduction of new equipment, materials and technologies.

 

  • Work closely with Key Opinion Leaders (KOL’s), physicians and product managers to develop innovative medical devices to improve patient care.

 

 

  • Project lead for assigned research & development projects including technical and project management responsibly.
    • Manage and drive project tasks to ensure timely completion of project milestones.
    • Work closely with cross functional groups to achieve project and company goals.
    • Product performance evaluations.
    • Contribute to innovation and creativity within team through filing of disclosures and patents.
    • Hold regular project meetings and document minutes and actions.
    • Ensure project milestones are achieved to meet business metrics.

 

 

 

  • Compliance with Quality, Regulatory and company policies and systems.
  • Communications:
    • Regular communication to cross-functional teams, senior management and business unit leaders.
    • Project status communications and reporting.
  • Remain on the forefront of emerging industry practice

 

 

  • Educating oneself in the medical area for which the new devices are being developed in order to have an appreciation for what needs to be achieved with these products.
  • Support other cross functional groups to deliver company goals.#
  • Ensure that Cook’s Code of Conduct is considered in all business matters carried out on Cook’s behalf.

 

Qualifications

  • Third level degree in Mechanical, Biomedical, Design, Chemical Engineering or similar discipline.
  • 2 Years design experience medical device roles.
  • Project planning skills.
  • Execution of project in a timely effective manner.
  • Knowledge of anatomy and physiology.
  • Good mechanical design and understanding of engineering fundamentals with extensive medical device materials knowledge.
  • Manufacturing design and process understanding.
  • Good working knowledge of Solidworks and/or Pro Engineer CAD.
  • Strong technical writer.
  • Knowledge of medical device quality & regulatory systems and medical device directives (ISO13485 and FDA CFR 820), EU Medical Device Regulation 2017/745.
  • Team Player with ability to develop strong working relationships.
  • Strong communication and inter-personal skills.
  • Good problem solving skills.
  • Highly motivated individual, self-starter with a passion for excellence.
  • Must be able to work in a fast paced environment.
  • Willingness and availability to travel on company business.

 

 

 

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Manufacturing Team Member

Cook Group

Limerick
30+ days ago
Limerick
30+ days ago

The primary function is to assist in the manufacturing & shipment of medical device products.

 

Reporting to: Production Supervisor  

 

 

Find out more about Cook Medical here


  • Carry out any process steps required for the manufacture & shipment of high quality medical devices products.
  • Adherence to COOK Quality system procedures and all associated manufacturing documentation which is provided to employees in order to assist them in the manufacture & shipment of high quality products.
  • Responsible for the completion of training in relation to the manufacture & shipment of product.
  • Ensure that a high standard of GMP and housekeeping is maintained in all manufacturing areas.
  • Adherence to all Environmental, Health and Safety requirements in accordance with company Policies.
  • Highlight any potential issues to team leaders/Supervisors.
  • Provide flexibility in working on any other tasks that may arise during the course of a normal day in a production environment.
  • May perform other duties as assigned by Supervisor.
  • Working as part of a team within the Production area.
  • Ensure that Cook’s Code of Conduct is considered in all business matters carried out on Cook’s behalf.

  • Experience in a production environment preferred.
  • Previous experience in medical devices, while not essential is advantageous.
  • Good communication and inter-personal skills.
  • Ability to work as part of a team.
  • Some flexibility as regards working hours/days.
  • Willingness and availability to travel on company business
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Manufacturing Team Member

Cook Group

Limerick
30+ days ago
Limerick
30+ days ago

Overview

The primary function is to assist in the manufacturing & shipment of medical device products.

 

Reporting to: Production Supervisor  

 

 

Find out more about Cook Medical here

Responsibilities

  • Carry out any process steps required for the manufacture & shipment of high quality medical devices products.
  • Adherence to COOK Quality system procedures and all associated manufacturing documentation which is provided to employees in order to assist them in the manufacture & shipment of high quality products.
  • Responsible for the completion of training in relation to the manufacture & shipment of product.
  • Ensure that a high standard of GMP and housekeeping is maintained in all manufacturing areas.
  • Adherence to all Environmental, Health and Safety requirements in accordance with company Policies.
  • Highlight any potential issues to team leaders/Supervisors.
  • Provide flexibility in working on any other tasks that may arise during the course of a normal day in a production environment.
  • May perform other duties as assigned by Supervisor.
  • Working as part of a team within the Production area.
  • Ensure that Cook’s Code of Conduct is considered in all business matters carried out on Cook’s behalf.

Qualifications

  • Experience in a production environment preferred.
  • Previous experience in medical devices, while not essential is advantageous.
  • Good communication and inter-personal skills.
  • Ability to work as part of a team.
  • Some flexibility as regards working hours/days.
  • Willingness and availability to travel on company business

Posted

22 days ago

Description

Design, development and taking to market of medical devices for one or more Cook Medical Strategic Business Units.

 

 

Reporting to: Senior Research & Development Engineer/Research & Development Manager  

 

 

 

Find out more about Cook Medical here


  • Perform Duties of Research & Development Engineer including:
    • Design development, prototyping, test method design, design evaluation, design reviews, design specifications, design verification and validation, design protocols and reports, transfer to production activities in a timely effective manner.
    • Product testing and evaluation, completion of test reports to support design selection.
    • Preparation and presentation of design reviews.
    • Product and project risk analysis and risk management.
    • Work with Process Development Engineering to introduce/develop new equipment and production processes as required for any new manufacturing techniques.
    • Source new materials components and equipment.
    • Development of component specifications, inspection methods, bills of materials and manufacturing processes.
    • Introduction of new equipment, materials and technologies.

 

  • Work closely with Key Opinion Leaders (KOL’s), physicians and product managers to develop innovative medical devices to improve patient care.

 

 

  • Project lead for assigned research & development projects including technical and project management responsibly.
    • Manage and drive project tasks to ensure timely completion of project milestones.
    • Work closely with cross functional groups to achieve project and company goals.
    • Product performance evaluations.
    • Contribute to innovation and creativity within team through filing of disclosures and patents.
    • Hold regular project meetings and document minutes and actions.
    • Ensure project milestones are achieved to meet business metrics.

 

 

 

  • Compliance with Quality, Regulatory and company policies and systems.
  • Communications:
    • Regular communication to cross-functional teams, senior management and business unit leaders.
    • Project status communications and reporting.
  • Remain on the forefront of emerging industry practice

 

 

  • Educating oneself in the medical area for which the new devices are being developed in order to have an appreciation for what needs to be achieved with these products.
  • Support other cross functional groups to deliver company goals.#
  • Ensure that Cook’s Code of Conduct is considered in all business matters carried out on Cook’s behalf.

 


  • Third level degree in Mechanical, Biomedical, Design, Chemical Engineering or similar discipline.
  • 2 Years design experience medical device roles.
  • Project planning skills.
  • Execution of project in a timely effective manner.
  • Knowledge of anatomy and physiology.
  • Good mechanical design and understanding of engineering fundamentals with extensive medical device materials knowledge.
  • Manufacturing design and process understanding.
  • Good working knowledge of Solidworks and/or Pro Engineer CAD.
  • Strong technical writer.
  • Knowledge of medical device quality & regulatory systems and medical device directives (ISO13485 and FDA CFR 820), EU Medical Device Regulation 2017/745.
  • Team Player with ability to develop strong working relationships.
  • Strong communication and inter-personal skills.
  • Good problem solving skills.
  • Highly motivated individual, self-starter with a passion for excellence.
  • Must be able to work in a fast paced environment.
  • Willingness and availability to travel on company business.

 

 

 

Source: Cook Group