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Regulatory Affairs Specialist-Ii-Et

4-7 years
Not Disclosed
10 April 4, 2025
Job Description
Job Type: Hybrid 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 Title:

Regulatory Affairs Specialist-II

Company:

Medtronic

Location:

Nanakramguda, Hyderabad, India (Hybrid)

Job Type:

Full-time

 

 


Job Summary:

As a Regulatory Affairs Specialist-II at Medtronic, you'll support the design and development of medical devices by ensuring compliance with global regulatory requirements. This role combines strategic planning with execution in a collaborative environment, and offers numerous opportunities for professional growth, skill development, and global impact.


Key Responsibilities:

  • Prepare, review, and file premarket documents for global registrations.

  • Collaborate with business units and international regulatory teams for marketing authorizations.

  • Review pre-clinical and clinical protocols and reports for submissions.

  • Develop regulatory strategies for new or modified products.

  • Monitor and assess regulatory changes and their impact.

  • Communicate with global health authorities.

  • Prepare internal documentation related to product modifications.

  • Support audits and inspections by health agencies.

  • Author/review regulatory procedures and update as needed.

  • Evaluate regulatory impact of change control documents.

  • Maintain regulatory records and systems.

  • Review promotional materials for regulatory compliance.

  • Ensure compliance of materials and prototypes to regulatory standards.


Minimum Qualifications:

  • Bachelor’s degree in Medical, Mechanical, Electrical, Life Sciences, or other healthcare-related disciplines.

  • 4–7 years of experience in Regulatory Affairs in the medical device or pharmaceutical industry.

  • Strong understanding of India, US FDA, and EU regulations.

  • Excellent communication, organization, and writing skills.

  • High attention to detail and ability to manage multiple tasks.

  • Strong English language proficiency (reading, writing, speaking).

  • A proactive learner with a team-oriented attitude.


Preferred Qualifications ("Nice to Haves"):

  • Global regulatory affairs knowledge and experience.

  • Experience with cross-functional teams.

  • Problem-solving and project management experience.

  • Ability to manage projects to completion independently.

  • Strong interpersonal, influencing, and negotiation skills.

  • Familiarity with RAPS Regulatory Affairs Certification (RAC).

  • Experience in fast-paced, dynamic work environments.


Physical Job Requirements:

  • This description outlines general responsibilities but is not exhaustive of all duties and skills required for the role.


Benefits & Compensation:

  • Competitive salary and flexible benefits package.

  • Career growth and development programs.

  • A culture that values employee contributions and supports work-life balance.


About Medtronic:

Medtronic is a global leader in healthcare technology with over 90,000 employees worldwide. Their mission is to alleviate pain, restore health, and extend life. Medtronic fosters a culture of innovation, inclusion, and collaboration, empowering employees to engineer solutions that impact lives globally.