Skip to main content
Post your CV and find your next job on Indeed!

Medical Devices Research jobs

Sort by: -
    • Experience in a regulated manufacturing environment; medical device experience is highly desirable.
    • We are seeking a hands-on R&D Process Technician to join…
    • Reporting to the Eyecare Technical Lead and the Director of the Technical Centre, you will lead cross-functional teams — spanning Operations, Global Program…
    • View all AbbVie jobs - Westport jobs - Scientist jobs in Westport, County Mayo
    • Salary Search: Process Scientist salaries in Westport, County Mayo
    • See popular questions & answers about AbbVie
    • You will have experience in a pharmaceutical, biotechnology, medical device, technical operations, manufacturing, or regulated laboratory environment.
    • Co-operate in evaluating assays, equipment, consumable items and research projects.
    • Full-time (35 hours per week).
    • Values and strategic plan of the Hospital.
    • Lead and support Risk Management activities throughout the product development lifecycle for medical devices and combination products.
    • In this leadership role, you will lead a dedicated team of electronic and electrical engineers responsible for the development and support of sophisticated…
    • Experience in medical devices or another highly regulated environment.
    • This is a senior role leading complex, cross-functional product development and…
    • Maintain detailed awareness and understanding of global risk management requirements for medical devices and drug-device combination products in regions of…
    • Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
    • They will work to process, analyse and report results of…
    • Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
    • Act as the sponsor's main contact person in all matters…
    • Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
    • This is an exciting opportunity to work within a fast paced,…
    • Support the preparation of prototypes, fixtures, equipment, and test records for medical-device verification and applicable IEC 60601 testing under engineering…
    • Consumer electronics experience is preferred, but candidates from medical devices, automotive, aerospace, or other technically rigorous industries with relevant…
    • Translate scientific and technological advances into differentiated service offerings for clinical research and patient-facing care.
    • The purpose of this role is to provide technical support for electronic manufacturing test systems and associated equipment used in the production of medical…
R&D Process Technician
Athlone, County Westmeath
Permanent, Full-time

Job details

Pay information not provided
Company pension, Private medical insurance, On-site parking
Permanent, Full-time
Athlone, County Westmeath

Full job description

We are seeking a hands-on R&D Process Technician to join our client's growing medical device manufacturing start-up in Ireland. Working closely with R&D, Process Engineering, Quality and Operations, you will support process development, equipment testing, troubleshooting and manufacturing scale-up, helping transform new product concepts into reliable, repeatable and scalable manufacturing processes within a regulated environment.

Key Responsibilities:

  • Conduct engineering tests and experiments, analyse data and prepare technical reports.
  • Operate, troubleshoot, calibrate and maintain manufacturing and R&D equipment, tooling and test systems.
  • Support process development, optimisation, equipment qualification and process validation.
  • Investigate technical issues, identify root causes and implement improvements to product quality, process reliability and manufacturing efficiency.
  • Assist with the introduction of new equipment, tooling and manufacturing methods, including the transfer of new products into production.
  • Maintain accurate technical records, SOPs, work instructions and equipment documentation in line with quality and regulatory requirements.
  • Ensure all activities comply with health and safety requirements and established quality standards.

Requirements:

  • Diploma, degree or equivalent qualification in Mechanical, Biomedical, Manufacturing or Process Engineering, or a related discipline.
  • Minimum of 2 years’ relevant experience in R&D, process engineering, manufacturing or equipment engineering.
  • Experience in a regulated manufacturing environment; medical device experience is highly desirable.
  • Hands-on experience with manufacturing equipment, test systems, fixtures or tooling.
  • Strong technical problem-solving skills, with experience in engineering testing, data analysis and technical documentation.
  • Familiarity with SOPs, controlled documentation and quality management systems.
  • An understanding of process development, equipment qualification and process validation.
  • Excellent communication and teamwork skills, with the ability to work independently and adapt to a fast-paced start-up environment.

This is an opportunity to play a hands-on role in developing manufacturing capabilities within a growing medical device business, contributing directly to product development, process improvement and manufacturing scale-up.

For more information or to apply, please contact: Aoife Regan

Email: aoife.regan@collinsmcnicholas.ie

Phone: (090) 6450 760

CMCNPRO1

Benefits:

  • Company pension
  • On-site parking
  • Private medical insurance

Work Location: In person

Let Employers Find YouUpload Your Resume