India jobs / Regulatory Documentation

Regulatory Documentation jobs

Explore 13 current openings. Compare roles, companies, locations, and work options, then open any job to view the full details.

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Current openings

Showing 20 jobs

  1. Senior Regulatory Documentation Coordinator

    IQVIA (formally Quintiles IMS)

    Supports compilation, publishing, and QC of regulatory submissions. Handles dossier assembly, electronic submissions (eCTD, NeeS), bookmarking, hyperlinking, TOC per HA guidelines. Collects CSR appendices per ICH. …

    Bangalore, IndiaOn-siteFull-time
    Active

  2. Senior Regulatory Affairs Specialist

    Medtronic

    Senior Regulatory Affairs Specialist at Medtronic responsible for leading regulatory strategy, documentation, and submissions for medical device projects. Works with cross-functional teams to prepare global pre‑market …

    Nanakramguda, Hyderabad, IndiaHybridFull-time
    Active

  3. Senior Regulatory Document Coordinator

    IQVIA (formally Quintiles IMS)

    Supports the preparation and coordination of regulatory documents and submissions, working under senior guidance. Requires a high school diploma or equivalent, with a preference for a science degree in biology, …

    Bangalore, IndiaOn-siteFull-time
    Active

  4. R&D Electronic Document Specialist

    Sanofi

    R&D Electronic Document Specialist at Sanofi Hyderabad is responsible for preparing, formatting, and validating regulatory documents for electronic submissions such as eCTD, INDs, and NDAs. The role requires mastery of …

    Hyderabad, IndiaOn-siteFull-time
    Active

  5. Senior Regulatory Document Coordinator

    IQVIA (formally Quintiles IMS)

    Senior Regulatory Document Coordinator responsible for compiling, publishing, and quality controlling regulatory submissions, ensuring compliance with GCP and ICH guidelines, and supporting electronic dossier creation.

    Bangalore, IndiaOn-siteFull-time
    Active

  6. Regulatory Affairs Associate I

    AstraZeneca

    Regulatory Affairs Associate I at AstraZeneca supports drug development by managing regulatory submissions, document tracking, and interfacing with health authorities. The role involves preparing and executing simple …

    Bangalore, IndiaHybridFull-time
    Active

  7. Technical Business Analyst

    Synechron

    Synechron seeks proactive Technical Business Analyst for FinTech product dev. Gather, analyze, document business & technical requirements for digital payments, wallets, trading systems. Work Agile with product owners, …

    Bengaluru, IndiaOn-siteFull-time
    Active

  8. Regulatory Affairs Specialist

    Medtronic

    Support design and development control, prepare and review premarket documents, collaborate with global regulatory teams, develop regulatory strategies, monitor regulatory changes, maintain communication with health …

    Nanakramguda, Hyderabad, IndiaHybridFull-time
    Active

  9. Medical Documents Filing/Abstract / Medical documentation/ Medical records

    ARstrat

    Medical Documents Filing/Abstract team at ARstrat focuses on organizing and indexing scanned medical records to support clinical workflows. The role maintains a structured filing system, assigns file names, folders, and …

    Bangalore,IND,IndiaFull-time
    Active

  10. Lead Specialist, Regulatory Affairs

    Gehc

    Lead Specialist, Regulatory Affairs at GE Healthcare Global Private Limited focuses on obtaining and maintaining global third‑party supplier documentation for Imaging Accessories & Supplies products. The role …

    Gurgaon, IndiaOn-siteFull-time
    Active

  11. Regulatory Affairs Specialist

    Medtronic

    Support design and development control activities, prepare and review pre‑market documents, collaborate with global regulatory teams, develop regulatory strategies, monitor regulatory changes, maintain communication …

    Nanakramguda, Hyderabad, IndiaOn-siteFull-time
    Active

  12. Document Controller

    Jones Lang LaSalle

    Document Control team at JLL ensures the Integrated Management System documents are accurate, stored securely, and compliant with ISO standards. The role supports the Management Representative by managing document …

    Bengaluru, KA, IndiaOn-siteFull-time
    Active

  13. Document Controller

    GE Vernova

    Document Control Team at GE Vernova ensures project documentation is accurate, up‑to‑date, and accessible throughout the project lifecycle, supporting quality and process improvement initiatives. The role maintains and …

    Noida,IndiaOn-siteFull-time
    Active

  14. Lead Regulatory Affairs Specialist

    Becton Dickinson

    Lead Regulatory Affairs Specialist at Becton Dickinson responsible for independently supporting projects to bring new and modified medical devices to market, ensuring ongoing compliance. Leads development of global …

    Bengaluru, IndiaOn-siteFull-time
    Active

  15. Document Controller

    :q Realty

    Create and process Purchase Orders, amendments, and EOTs in SAP. Book bills via SES and GRN, ensuring accurate cost centers and codes. Initiate budget transfers, follow up approvals, resolve SAP issues. Manage Purchase …

    Gurgaon, Haryana, IndiaOn-siteFull-time
    Active

  16. RA CMC Manager

    Novartis

    RA CMC Manager responsible for regulatory activities related to chemistry, manufacturing, and control (CMC). Leads global CMC regulatory strategy, planning, authoring, reviewing, coordinating, and submitting CMC …

    Hyderabad, IndiaOn-siteFull-time
    Active

  17. Document Controller

    SNC-Lavalin

    Document Controller at WS Atkins (India) Private Limited in Pune, India. The role maintains the Master Document Register, verifies drawings and specifications, and manages filing on Aconex and SharePoint to keep project …

    Pune,IN,IndiaFull-time
    Active

  18. Associate Regulatory Operations

    Abbott

    Associate Regulatory Operations is responsible for processing submission documents, ensuring compliance with regulatory formatting standards, and performing quality checks on team outputs. The role collaborates with …

    Mumbai, IndiaOn-siteFull-time
    Active

  19. Document Specialist

    ProPharma Group

    ProPharma Group seeks a Document Specialist to support regulatory document preparation and eCTD publishing for clients in the pharmaceutical and biotech sectors. The role involves formatting, reviewing, and converting …

    Hyderabad, IndiaOn-siteFull-time
    Active

  20. Document Controller

    SURBANA

    Document Controller at Surbana Jurong India Private Limited manages and maintains all project documents, ensuring proper version control and compliance with documentation standards. The role coordinates with engineers, …

    Ahmedabad,IndiaOn-siteFull-time
    Active