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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