Medtronic is a global leader in medical technology, services, and solutions, committed to improving healthcare access and equity worldwide. With a strong focus on innovation and compassion, Medtronic empowers employees to lead with purpose and drive meaningful change in patient care.
Join a company that values your contributions and offers a dynamic work environment with opportunities for professional growth.
Job Description
Key Responsibilities:
- Monitor and manage the company’s medical device surveillance program, including intake, evaluation, and follow-up on adverse event reports.
- Ensure accurate maintenance and reporting of Medical Device Reports (MDRs) in compliance with regulatory requirements.
- Review and analyze clinical databases to extract Adverse Drug Experience (ADE) data for safety summaries.
- Act as a liaison between internal teams and external collaborators to meet regulatory reporting standards.
- Assist in resolving legal liabilities related to adverse event reporting.
- Provide guidance to junior professionals and support cross-functional projects.
Qualifications & Experience:
- Bachelor’s degree (or equivalent as per U.S. immigration standards).
- Minimum 2 years of relevant experience in pharmacovigilance, medical device vigilance, or regulatory compliance.
- Advanced degree (preferred for candidates with less experience).
- Strong analytical skills with attention to detail.
- Knowledge of FDA/EU MDR regulations is a plus.
Career Growth & Benefits:
- Competitive salary & flexible benefits package.
- Opportunities for professional development and mentorship.
- Work in a collaborative, innovative environment with a global impact.
How to Apply
Application Link For MDR/Vigilance Specialist II
Application Link For MDR/Vigilance Specialist I
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