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

Science Medical jobs in Galway, County Galway

Sort by: -
    • Knowledge of basic anatomy, physiology, and medical terminology.
    • 1-2 years relevant experience in a medical devices or related environment preferred.
    • This role will involve carrying out Plant-wide Internal Audits as per relevant schedules; Controlling closed Exception Reports/ Non Conformance Reports, Line…
    • Minimum 5-7 years of experience in medical device industry with minimum 5 years of progressively responsible positions.
    • Audit experience would an advantage.
    • View all Abbott Laboratories jobs - Galway jobs - Senior Quality Engineer jobs in Galway, County Galway
    • Salary Search: Senior Quality Engineer - Fixed Term Contract salaries in Galway, County Galway
    • See popular questions & answers about Abbott Laboratories
    • BE + ME Mechanical Engineering.
    • BE + ME Electronic & Computer Engineering.
    • Provide daily technical support to the department.
    • At our Quality Department in Medtronic, plc, we focus on supporting the product value stream to ensure that customer and patient needs are met every day.
    • This role is based in the company’s European facility in Athenry on our Day Shift. .
    • Day shift hours are Monday - Thursday 7am - 3:30pm and 7am - 1pm on…
    • Experience within a regulated industry such as medical devices, pharmaceuticals, supplements, cosmetics or a similar environment.
    • Position Title : Senior Programme Support Associate.
    • Classification : General Service Staff, G7.
    • Type of Appointment : *Special Short Term Graded Contract…
    • The team works with various software technologies in application software, network software, mobile software, BT/BLE communication software, and interfacing…
    • From secure device connectivity and real-time data platforms to intelligent clinical tools and patient-facing experiences, PCS transforms complex cardiac data…
    • The team works with various software technologies in application software, network software, mobile software, BT/BLE communication software, and interfacing…
    • Experience developing software within regulated environments, including medical device development.
    • Knowledge of software development standards and regulatory…
    • The team works with various software technologies in application software, network software, mobile software, BT/BLE communication software, and interfacing…
    • Bachelor's degree (or equivalent) in a science-related discipline.
    • Develop and implement global CMC regulatory strategies for injectable products.
    • At Boston Scientific, we are looking for an ambitious graduate to support the design, development, coordination, and delivery of capability-building initiatives…

Job Post Details

Associate MDR/Vigilance Specialist - job post

PE Global
4.0 out of 5 stars
Galway, County GalwayHybrid work
Full-time

Job details

Job type

  • Full-time

Location

Galway, County GalwayHybrid work

Full job description

The Role

PE Global are recruiting for an Associate MDR/Vigilance Specialist for our medical device client based in Galway. This is a 23-month contract role. Hybrid working options.

Job Responsibilities

  • Monitors the company's drug or medical devices surveillance program including the intake, protocol development, evaluation, processing, and follow-up on adverse reports, participation in the resolution of any legal liability and in complying with government regulations.
  • Ensures complete and accurate maintenance and reporting of Medical Device Reports (MDRs), Adverse Drug Experience (ADE) data or adverse reaction data as required by regulatory agencies.
  • Review and analyze clinical databases for the extraction of ADE data and integrates the data to ensure the creation of a unified database consistent with the aims and purposes of ADE standardization and internalization as well as to ensure the accuracy and quality of safety summaries.
  • Acts as a liaison internally and with external collaborators to develop programs and processes to meet regulatory reporting requirements.

Education & Experience

  • Bachelor's degree (Level 8 NFQ) in Engineering/ Science/ Legal/ Clinical or related discipline.
  • 1-2 years relevant experience in a medical devices or related environment preferred.
  • Dynamic team player who can work effectively and proactively on cross functional teams.
  • Ability to think critically and make sound decisions.
  • Strong attention to detail
  • Knowledge of basic anatomy, physiology, and medical terminology
  • Must be focused on patient safety and customer service, set high standards, instil operational excellence, drive accountability and model ethical behaviour.
  • Good communicator and fluent in English, both in writing and speaking


Interested candidates should submit an updated CV.

Please click the link below to apply, alternatively send an up-to-date CV aisling.oleary@peglobal.net

****Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland****

Let Employers Find YouUpload Your Resume