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Regulatory Affairs Manager (Cmc)

Amgen
8-13 years
Not Disclosed
Hyderabad
1 June 3, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding

Regulatory Affairs Manager (CMC)

Location: Hyderabad, India
Work Type: On-Site
Department: Regulatory Affairs – Chemistry, Manufacturing & Controls (CMC)

Position Summary

The Regulatory Affairs (CMC) Manager is responsible for the execution and coordination of global regulatory CMC activities for assigned commercial products. This role provides leadership, guidance, and regulatory expertise to ensure successful implementation of CMC regulatory strategies and regulatory compliance throughout the product lifecycle.

The position collaborates closely with cross-functional teams across development, manufacturing, quality, operations, commercial functions, and regional regulatory teams to support global submissions, change management activities, and health authority interactions.


Key Responsibilities

Regulatory Strategy & Execution

  • Develop and execute global and country-specific CMC regulatory strategies for assigned products.

  • Provide strategic regulatory input and risk assessments to product teams.

  • Define regulatory filing requirements and submission strategies.

  • Identify potential regulatory risks and develop mitigation plans.

  • Execute regulatory strategies in alignment with business objectives and regulatory requirements.

  • Communicate regulatory strategies, risks, and critical issues to senior management.


Submission Planning & Regulatory Documentation

  • Lead preparation and coordination of CMC regulatory submissions.

  • Develop global CMC dossiers for:

    • Initial Marketing Applications

    • Variations

    • Amendments

    • Post-Approval Changes

  • Ensure submission content meets global regulatory requirements and quality standards.

  • Support regulatory filing activities across multiple markets.


Health Authority Interactions

  • Develop response strategies for regulatory agency inquiries.

  • Coordinate preparation and submission of responses to health authority questions.

  • Support interactions with global regulatory authorities regarding CMC matters.

  • Ensure timely and compliant communication with regulatory agencies.


Product Team Leadership

  • Serve as Product Lead or Principal Regulatory Representative for assigned products.

  • Participate in cross-functional product teams and provide CMC regulatory expertise.

  • Support product development, lifecycle management, and commercialization activities.

  • Provide strategic recommendations regarding regulatory pathways and compliance requirements.


Change Management

  • Support manufacturing, process, analytical, and quality-related change management activities.

  • Assess regulatory impact of proposed changes.

  • Ensure appropriate regulatory filings are identified and executed.

  • Coordinate implementation of regulatory requirements related to product changes.


Cross-Functional Collaboration

  • Partner with teams across:

    • Development

    • Manufacturing

    • Quality Assurance

    • Quality Control

    • Supply Chain

    • Operations

    • Commercial Functions

  • Ensure alignment of regulatory strategies, timelines, execution plans, and supply requirements.

  • Collaborate with local regulatory teams to support global and regional filing strategies.

  • Facilitate communication between global and regional stakeholders.


Regulatory Compliance & Process Management

  • Ensure compliance with established regulatory processes and procedures.

  • Maintain alignment across products and programs through standardized practices.

  • Monitor evolving regulatory requirements and industry guidance.

  • Incorporate new regulatory expectations into product strategies and regulatory planning.

  • Identify opportunities for process optimization and continuous improvement.


Regulatory Information Management

  • Maintain accurate regulatory records and submission data.

  • Support regulatory tracking and reporting activities.

  • Ensure information is current and accurately maintained within Regulatory Information Management (RIM) systems.

  • Monitor departmental deliverables and regulatory milestones.


Continuous Improvement

  • Identify process improvement opportunities within Regulatory Affairs CMC.

  • Contribute to enhancement of regulatory systems, tools, and workflows.

  • Support implementation of organizational and regulatory process changes.

  • Drive efficiencies while maintaining compliance and quality standards.


Required Qualifications

Education

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Chemistry

    • Biochemistry

    • Engineering

    • Related Scientific Discipline

Experience

  • 8–13 years of directly related professional experience.

  • Experience in one or more of the following areas:

    • Manufacturing Operations

    • Quality Control (QC)

    • Quality Assurance (QA)

    • Clinical Manufacturing Support

    • Supply Chain or Distribution

    • Regulatory Affairs