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Regulatory Affairs Manager (Cmc)

0-2 years
Not Disclosed
10 Sept. 15, 2025
Job Description
Job Type: Full Time Education: B.Sc/ M.Sc/ M.Pharm/ B.Pharm/ 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

Job Title

Manager (CMC)

Location

  • India – Hyderabad

  • Work Location Type: On Site

Job ID

R-224460

Date Posted

August 29, 2025

Category

Regulatory


Role Overview

The Regulatory Affairs (RA) CMC Manager is responsible for coordinating and executing global regulatory CMC (Chemistry, Manufacturing & Controls) activities. This includes providing leadership, regulatory guidance, and oversight to ensure successful implementation of regulatory strategies for assigned commercial products. The role requires effective communication of strategy, risks, and issues to senior management, as well as collaboration with site and regional CMC representatives to deliver global regulatory outcomes.


Key Activities

  • Act as product lead or principal for one or more products.

  • Provide strategic regulatory input and conduct regulatory risk assessments for product teams.

  • Execute regulatory strategy in line with submission preparation requirements.

  • Ensure compliance with RA CMC processes and identify opportunities for improvement.

  • Incorporate updates from external regulatory guidance into internal strategies.

  • Report regulatory issues and process needs to RA CMC product team management.


Key Responsibilities

  • Develop and execute global and country-specific regulatory strategies.

  • Define minimal regulatory filing requirements, submission strategy, and risk assessments.

  • Prepare global CMC dossiers for initial submissions, variations, and amendments.

  • Support change management activities.

  • Develop strategies and responses to health authority queries.

  • Collaborate with development, operations, and commercial teams to ensure strategy alignment and supply continuity.

  • Align filing strategies with local regulatory teams.

  • Maintain accurate and current submission data in Regulatory Information Management (RIM) systems.

  • Follow established processes to ensure consistency and alignment across products.


Knowledge & Skills

  • Strong knowledge and hands-on experience in CMC-specific regulatory affairs.

  • Familiarity with manufacturing, testing (QC/QA or clinical), or distribution processes.

  • Ability to assess and manage regulatory risks.

  • Effective communication and cross-functional collaboration skills.


Education & Experience

  • Doctorate degree; OR

  • Master’s degree with minimum 3 years of directly related experience; OR

  • Bachelor’s degree with minimum 5 years of directly related experience.

  • Prior Regulatory CMC experience is required.