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Mdr/Vigilance Specialist I

0-2 years
Not Disclosed
10 June 13, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Summary

Medtronic, a global leader in healthcare technology, seeks an MDR/Vigilance Specialist I for its Hyderabad facility. In this hybrid role, you will monitor medical device and drug surveillance programs to ensure timely and accurate reporting of adverse events. This entry-level position is perfect for candidates passionate about regulatory compliance, pharmacovigilance, and patient safety in the clinical research and medical device sectors.


Key Responsibilities

  • Monitor and manage the company’s medical device and drug surveillance programs.

  • Ensure accurate intake, evaluation, processing, and follow-up of adverse event reports.

  • Comply with government regulations regarding Medical Device Reports (MDRs) and Adverse Drug Experience (ADE) data.

  • Analyze clinical databases for ADE data extraction and integration into unified safety summaries.

  • Collaborate with internal teams and external partners to develop regulatory reporting processes.

  • Deliver assigned projects and contribute to process improvements under supervision.

  • Communicate effectively with internal stakeholders to gather and share necessary information.


Required Skills & Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or equivalent.

  • 0 years of experience required (entry-level role).

  • Broad theoretical knowledge of pharmacovigilance and medical device vigilance processes.

  • Ability to follow established procedures and adapt to minor process improvements.

  • Strong communication skills for internal coordination.

  • Detail-oriented with analytical problem-solving abilities.

  • Familiarity with global regulatory guidelines for medical devices (desirable).


Perks & Benefits

  • Competitive salary package.

  • Flexible benefits tailored to career and life stages.

  • Access to global learning resources and training.

  • Strong culture of recognition and employee appreciation.

  • Hybrid work environment supporting work-life balance.


Company Description

Medtronic is a pioneering global healthcare technology leader, dedicated to solving the world's most complex health challenges. With over 95,000 professionals worldwide, Medtronic innovates in medical device development, R&D, and clinical safety, transforming healthcare solutions for better patient outcomes.


Work Mode

Hybrid (Nanakramguda, Hyderabad, India)


Call to Action

Begin your career in healthcare regulatory vigilance with Medtronic! Apply today to contribute to medical device and drug safety programs that impact millions globally.