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

Senior Specialist, Regulatory Affairs (Grade 16)

Baxter
8-10 years
INR 18 LPA – 30 LPA
Ahmedabad, India
1 July 2, 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 (Grade 16)

Company: Baxter
Location: Ahmedabad, Gujarat, India
Department: Regulatory Affairs
Job Type: Full-Time


JOB OVERVIEW

The Senior Specialist, Regulatory Affairs is responsible for developing and executing global regulatory strategies to obtain and maintain marketing authorizations for pharmaceutical products. The role supports regulatory submissions, lifecycle management, labeling, compliance activities, and cross-functional regulatory projects while ensuring compliance with global regulatory requirements. The position also provides regulatory guidance to project teams, manages regulatory risks, and coordinates interactions with health authorities to support product development and commercialization.


KEY RESPONSIBILITIES

Regulatory Strategy

  • Develop and execute global regulatory strategies for assigned products.

  • Prepare regulatory project plans and timelines.

  • Support product registration and lifecycle management.

  • Evaluate regulatory pathways for global markets.

  • Identify and mitigate regulatory risks.

Regulatory Submissions

  • Prepare, compile, review, and submit regulatory dossiers.

  • Coordinate global regulatory submissions.

  • Maintain marketing authorizations throughout the product lifecycle.

  • Ensure timely submission of regulatory documents.

  • Support new product registrations and post-approval submissions.

Regulatory Compliance

  • Monitor global regulatory requirements and guidelines.

  • Ensure compliance with applicable regulatory standards.

  • Maintain regulatory documentation and records.

  • Support regulatory inspections and audits.

  • Escalate compliance risks when necessary.

Health Authority Interactions

  • Respond to regulatory authority queries within required timelines.

  • Coordinate communications with global health authorities.

  • Provide regulatory support during agency interactions.

  • Ensure timely resolution of regulatory requests.

Product Lifecycle Management

  • Maintain existing regulatory approvals.

  • Support product variations, renewals, and amendments.

  • Manage post-approval regulatory activities.

  • Coordinate lifecycle regulatory documentation.

Labeling Management

  • Prepare, review, and approve product labeling.

  • Ensure labeling complies with global regulatory requirements.

  • Support labeling updates throughout the product lifecycle.

  • Review regulatory labeling documentation.

Quality Documentation

  • Prepare, review, and maintain Standard Operating Procedures (SOPs).

  • Maintain regulatory files and documentation.

  • Ensure document accuracy and version control.

  • Support quality management activities.

Cross-Functional Collaboration

  • Provide regulatory guidance to project teams.

  • Collaborate with Quality Assurance, R&D, Manufacturing, and Commercial teams.

  • Support global product development projects.

  • Participate in multidisciplinary project meetings.

Project Leadership

  • Represent Regulatory Affairs in project teams.

  • Lead small regulatory projects.

  • Manage multiple regulatory deliverables simultaneously.

  • Monitor project timelines and milestones.

Risk Management

  • Identify regulatory compliance risks.

  • Recommend mitigation strategies.

  • Monitor regulatory changes impacting products.

  • Escalate critical regulatory issues when necessary.


EDUCATIONAL QUALIFICATIONS

Required

  • Bachelor's Degree in a Scientific Discipline (or equivalent).

Preferred

  • Pharmacy

  • Pharmaceutical Sciences

  • Biotechnology

  • Biochemistry

  • Life Sciences

  • Chemistry

  • Related Scientific Discipline


EXPERIENCE REQUIREMENTS

Required

  • 8–10 years of total industry experience.

  • Minimum 2 years of Regulatory Affairs experience.

  • Experience in Pharmaceutical, Medical Device, CRO, or related healthcare industry.

  • Experience with global regulatory submissions.

  • Experience managing marketing authorizations.

Preferred

  • Experience with complex drug products.

  • Experience in biologics regulatory submissions.

  • Experience with peptides, liposomes, or iron colloids.

  • Experience in global regulatory strategy development.