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    Team Member LCM Job at Cipla

    Kickstart a rewarding regulatory career with the Team Member – LCM role in Vikhroli, Maharashtra. This Assistant Job position focuses on life cycle management activities for global non-respiratory product markets, ensuring compliance and uninterrupted supply across 150+ countries including the US, EU, South Africa, WHO, ANZ, and PEPFAR regions. Join a world-class team contributing to global business continuity and regulatory excellence. Build your career with cipla careers. Graduates searching for Pharma Jobs can apply.

    Introduction of the Job

    This Assistant Job role involves implementing Life Cycle Management activities for Non-respi products across global markets to ensure business continuity. The position supports regulatory compliance and post-approval activities across 150+ countries.

    Job Details

    • Designation: Team Member – LCM
    • Location: Vikhroli, Maharashtra, India
    • Posting Date: 22 Oct 2025
    • Req ID: 97010
    • Division: Not Specified
    • Department: Regulatory / LCM

    Responsible for non-respiratory product lifecycle management across US, EU, South Africa, ANZ, WHO, PEPFAR & 150+ global markets.

    About the Company

    A leading global pharmaceutical organization responsible for delivering medicines across multiple regulated and emerging markets while maintaining strong compliance and regulatory practices.

    Key Responsibilities for Assistant Job Role:

    • Assess global change requests per regulatory guidelines
    • Determine applicability of change and coordinate with QA, units, regional teams
    • Track and compile change request evaluations
    • Prepare variation packages (Module 2–5) & deficiency responses
    • Coordinate with API-RA, purchase, R&D, ADL, QA
    • Prepare annual reports (US) & WHO requalification dossiers
    • Compile re-registration dossiers and maintain document tracker
    • Save & maintain product database after change closure
    • Overcome documentation gaps through checklists
    • Key interactions with Manufacturing, Clinical, Purchase, R&D, QA, API suppliers

    Major Challenges for Assistant Job Role:

    • Inadequate documentation for evaluation of change requests and variations
    • Resolved by preparing checklist of required documents

    Educational Requirements for Assistant Job Role:

    • Minimum Graduate in Pharmacy

    Experience Requirements for Assistant Job Role:

    • Minimum 2 years in Regulatory Affairs / Quality Assurance / Quality Control / Manufacturing / Analytical Development / R&D

    Skills Required for Assistant Job Role:

    • Knowledge of regulatory procedures
    • Documentation & data compilation skills
    • Coordination & communication skills
    • Ability to track and manage multiple regulatory submissions

    How to Apply for Assistant Job Role:

    Graduates searching for Pharma Jobs can apply through cipla careers. Refer to the company career portal or recruitment contact for application submission.

    CLICK HERE TO APPLY ONLINE

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