Science Medical jobs in Galway, County Galway
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- PE GlobalGalway, County GalwayAd
- Knowledge of basic anatomy, physiology, and medical terminology.
- 1-2 years relevant experience in a medical devices or related environment preferred.
- Cregg Recruitment LtdGalway, County GalwayAd
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- MedtronicGalway, County Galway
- 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.
- Lifewave Europe LtdAthenry, County Galway
- Employee assistance program
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Ad- This role is based in the company’s European facility in Athenry on our Day Shift. .
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- Collins McNicholas RecruitmentAthenry, County Galway
- Company pension
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Ad- Experience within a regulated industry such as medical devices, pharmaceuticals, supplements, cosmetics or a similar environment.
- Collins McNicholas RecruitmentAthenry, County Galway
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Ad- Experience within a regulated industry such as medical devices, pharmaceuticals, supplements, cosmetics or a similar environment.
- UN International Organization for MigrationIreland
- Sick pay
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- MedtronicGalway, County Galway
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- MedtronicGalway, County Galway
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- MedtronicGalway, County Galway
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- MedtronicGalway, County Galway
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- ViatrisGalway, County Galway
- Bachelor's degree (or equivalent) in a science-related discipline.
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- Boston ScientificGalway, County Galway
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Job Post Details
Associate MDR/Vigilance Specialist - job post
4.04.0 out of 5 stars
Galway, County Galway•Hybrid work
Full-time
Job details
Job type
- Full-time
Location
Galway, County Galway•Hybrid 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****
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