| Position | Associate MDR Vigilance Specialist |
| Posted | 24 Jul 2026 |
| Expired | 23 Aug 2026 |
| Company | Sigmar Recruitment |
| Location | Galway | IE |
| Job Type | Full Time |
Latest job information from Sigmar Recruitment for the position of Associate MDR Vigilance Specialist. If the Associate MDR Vigilance Specialist vacancy in Galway matches your qualifications, please submit your latest application or CV directly through the updated Jobkos job portal.
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About Your New Employer Join a forward-thinking company committed to patient and product safety in the healthcare industry. Be part of a dynamic team focused on innovation and regulatory excellence in pharmaceutical and medical device oversight. Work in a supportive, collaborative environment designed to foster professional growth and knowledge development. About Your New Job As a Drug & Device Surveillance Specialist, you will: Monitor and manage drug and medical device surveillance programs, including the intake, protocol development, processing, and follow-up on adverse reports. Ensure thorough and accurate maintenance and regulatory reporting of Medical Device Reports (MDRs) and Adverse Drug Experience (ADE) data. Review and analyze clinical databases to extract and integrate ADE data, contributing to standardized and high-quality safety summaries. Act as a liaison with both internal teams and external partners to develop and refine compliance programs and fulfill regulatory reporting requirements. Deliver and manage assigned projects, primarily of limited scope, working under close supervision and within established guidelines. What Skills You Need Bachelors degree in a relevant scientific or healthcare discipline (or equivalent international qualification). Strong analytical and organizational skills with keen attention to detail. Effective communicator, able to interact confidently and professionally with internal and external stakeholders. What's on Offer Competitive salary and benefits package. Opportunities for mentorship, career development, and advancement within the company. The chance to start your career in a specialized, future-oriented area of drug and medical device safety. What's Next All applications are treated in strict confidence. Apply now by clicking the "Apply Now" button. If the role isnt quite right but youre interested in similar positions, please get in touch! We offer a range of opportunities across the pharmaceutical and medical device sectors. Skills: EMA regulations Regulatory affairs Surveillance MDR Benefits: Paid Holidays Parking Pension TPBN1_IJ
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