Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Sr Specialist Regulatory Affairs

Abbott
1+ years
8 LPA - 14 LPA
New Delhi, India
1 June 22, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Senior Specialist – Regulatory Affairs

Location: New Delhi, India
Company: Abbott
Department: Regulatory Affairs
Employment Type: Full-Time


Role Summary

The Senior Specialist – Regulatory Affairs is responsible for supporting regulatory strategy, product registrations, lifecycle management, and health authority interactions to ensure timely approvals and continued compliance of pharmaceutical, biologic, or medical device products.

This role serves as a key regulatory liaison across product development, manufacturing, quality, marketing, and regulatory agencies, ensuring that submissions, amendments, supplements, and regulatory documentation are prepared and maintained in accordance with global and local regulatory requirements.


Key Responsibilities

Regulatory Submissions & Product Registration

  • Prepare, review, and coordinate regulatory submissions for:

    • New Product Registrations

    • Supplements

    • Variations

    • Amendments

    • Renewals

    • Periodic Regulatory Reports

  • Ensure timely preparation and submission of regulatory dossiers.

  • Track submission progress and approval timelines.

Health Authority Interaction

  • Liaise with regulatory authorities to facilitate product approvals.

  • Respond to regulatory queries and deficiency letters.

  • Support meetings and communications with health authorities.

  • Monitor regulatory commitments and ensure timely closure.

Product Lifecycle Management

  • Support regulatory activities throughout the product lifecycle.

  • Manage post-approval changes and regulatory maintenance activities.

  • Ensure continued compliance of marketed products.

  • Assess regulatory impact of manufacturing, labeling, and formulation changes.

Regulatory Strategy Support

  • Contribute to regulatory strategy development and implementation.

  • Provide regulatory guidance during product development activities.

  • Support regulatory risk assessments and mitigation plans.

  • Assist in evaluating regulatory pathways for new products.

Cross-Functional Collaboration

  • Collaborate with:

    • Research & Development

    • Manufacturing

    • Quality Assurance

    • Marketing

    • Supply Chain

    • Regulatory Agencies

  • Act as regulatory representative within project teams.

  • Provide regulatory recommendations during product development and commercialization.

CMC & Compliance Support

  • Support Chemistry, Manufacturing & Controls (CMC) documentation and submissions.

  • Evaluate manufacturing and process changes for regulatory impact.

  • Ensure compliance with applicable regulations and guidelines.

  • Maintain regulatory documentation and submission records.

Labeling & Regulatory Documentation

  • Review and support:

    • Product Labels

    • Technical Documentation

    • Product Claims

    • Packaging Information

  • Ensure compliance with country-specific regulatory requirements.

  • Provide regulatory interpretation and guidance to internal stakeholders.


Required Qualifications

Education

  • Bachelor's Degree / Associate Degree in:

    • Pharmacy

    • Life Sciences

    • Biotechnology

    • Biomedical Sciences

    • Regulatory Affairs

    • Related Scientific Discipline


Experience

  • Minimum 1+ years of experience in:

    • Regulatory Affairs

    • Regulatory Submissions

    • Product Registration

    • Regulatory Compliance

Preferred Experience

  • Experience in:

    • Pharmaceuticals

    • Medical Devices

    • Biologics

    • Healthcare Industry

  • Exposure to product lifecycle management activities.