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

Manager - Regulatory Affairs - Crlb - Mumbai

7+ years
Not Disclosed
10 Nov. 11, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Manager - Regulatory Affairs (CRLB)

Location: Mumbai, India
Category: Regulatory Affairs


Role Summary / Purpose

  • Specialist professional individual contributor with comprehensive knowledge in Regulatory Affairs.

  • Executes highly complex or specialized projects.

  • Adapts existing precedents and may develop innovative solutions beyond traditional approaches.


Key Responsibilities

  • Act as a highly experienced resource within Regulatory Affairs for product registration submissions, progress reports, supplements, amendments, and periodic experience reports.

  • Interact with regulatory agencies to expedite pending approvals.

  • Serve as a regulatory liaison throughout the product lifecycle.

  • Participate in:

    • Product plan development and implementation

    • Regulatory strategy

    • Risk management

    • Chemistry, Manufacturing, and Control (CMC) processes

  • Ensure timely approval of new drugs, biologics, or medical devices and continued approval of marketed products.

  • Represent Regulatory Affairs to marketing, research teams, and regulatory agencies.

  • Advise development and/or marketing teams on:

    • Manufacturing changes

    • Line extensions

    • Technical labeling

    • Regulatory compliance and interpretations


Qualifications

  • Education:

    • Associate Degree (±13 years) or equivalent

  • Experience:

    • Minimum 7 years in Regulatory Affairs or relevant pharmaceutical/biopharma experience