Drug Safety & MDR Vigilance Analyst

Hero Recruitment Group; Galway; On-site; EUR 35,000 - 45,000; Full time

Job summary

Hero Recruitment Group is seeking a detail‑oriented regulatory affairs professional to join our Galway team. This entry‑level role focuses on pharmacovigilance, processing adverse event reports, and ensuring MDR/ADE data complies with regulations.

You will collaborate with internal teams and external partners to meet reporting requirements, contribute to safety summaries, and develop specialised knowledge through on‑the‑job training and project delivery from design to implementation.

Qualifications

• Requires broad theoretical knowledge typically obtained through advanced education.
• Bachelor's degree (or equivalent) required.
• No professional experience required.

Responsibilities

• Monitor pharmacovigilance or medical device surveillance programme and manage adverse event reports.
• Ensure regulatory reporting of Medical Device Reports (MDRs) and ADE data.
• Collaborate with internal/external teams to meet regulatory reporting requirements.

Skills

Regulatory knowledge

Adverse event reporting

Data reporting

Quality awareness

Education

Bachelor's degree or equivalent

Job description

Hero Recruitment Group is seeking a detail‑oriented regulatory affairs professional to join our Galway team. This entry‑level role focuses on pharmacovigilance, processing adverse event reports, and ensuring MDR/ADE data complies with regulations.

You will collaborate with internal teams and external partners to meet reporting requirements, contribute to safety summaries, and develop specialised knowledge through on‑the‑job training and project delivery from design to implementation.