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    Job · 21684973

    AHMEDABAD · FULLTIME

    Sr Executive, Drug Device Combination Product

    Amneal Pharmaceuticals

    Amneal Pharmaceuticals

    Ahmedabad · onsite · Posted 1d ago

    Sourced fromNaukri
    Undisclosed5–8 yrsfulltimeAhmedabad

    About a minute. You'll make an account on the way through.

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    Section · 01

    About this role

    Description:
    This role is responsible for developing and optimizing pharmaceutical packaging systems by applying scientific and engineering principles to ensure product protection, stability, compliance, and patient usability. The role contributes to design, selection, and qualification of primary and secondary packaging components aligned with product requirements, regulatory standards, and commercial considerations. The incumbent leads packaging development studies including compatibility, stability, and performance evaluations, and supports packaging validation and technology transfer activities. It collaborates with cross-functional teams to ensure timely and compliant product delivery. The role also evaluates new packaging technologies and materials, contributing to innovation, cost optimization, and continuous improvement within the product development lifecycle.

    Responsibilities:
    • Familiarity in the area of drug-device combination product development and regulatory requirements
      • Review change controls pertaining to DDCPs
        • Knowledge of QMSRs and ISO/ASTM standards including design controls for devices
          • Ability to work with cross-functional teams
          • Prepare and/or review DDCP documents including study protocols, reports, test procedures as per the QMSR requirements.
          • Coordinate with cross-functional teams including Quality Management and compile various elements of DHFs (Design History for drug device combination products.
          • Ensure conformance to the established Quality Management Systems Regulations for combination products.
          • Help draft Threshold/Comparative Analysis and Human Factors Study protocols
          • Provide support for identifying, preparing, and compiling the design transfer documents.
          • Prepare the risk management documents as per ISO 14971.
          • Interact with device development suppliers/third parties /testing institutions for the development of drug device combinations products as per the requirements.


    Additional Responsibilities:
    Education:
    • B. Pharm B. Pharm - Required
    • M. Pharm M. Pharm - Preferred
    Experience:
    • 5 years or more in 5 - 8 Years
    Specialized Knowledge: Licenses:


    Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

    Sourced from naukri

    Section · 02

    Skills

    Pharmaceutical Packagingtechnology transferProduct DeliveryComparative AnalysisRisk ManagementcomplianceProduct DevelopmentPharmaceuticalquality management

    Section · Company

    About Amneal Pharmaceuticals

    Amneal Pharmaceuticals

    Amneal Pharmaceuticals

    Pharma

    5.5k+

    employees

    2002

    24 years old

    Bridgewater, New Jersey

    United States (USA)

    About

    Amneal Pharmaceuticals operates in the pharmaceutical sector, focusing on developing accessible and affordable medicines to address critical healthcare challenges.

    Industries

    PharmaBiotechnologyClinical Research

    Employee ratings

    1,455 reviews

    4.2/ 5

    Culture

    4.0

    Career growth

    3.5

    Work-life

    4.2

    Employees rate it well for

    Work Culture190Senior Management93Work Life Balance87Work Environment69HR Policies65

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