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    Job · 21049314

    HYDERABAD · FULLTIME

    Submission Senior Specialist

    Bristol-Myers Squibb

    Bristol-Myers Squibb

    Hyderabad · onsite · Posted 8d ago

    Sourced fromFoundit
    Not disclosed6–8 yrsfulltimeHyderabad

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    Section · 01

    About this role

    At Bristol Myers Squibb, our employees often ask, Who are you working for—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

    Key Responsibilities

    • Tracks, collects and reviews all components for routine submissions to Health Authorities
    • Interacts with responsible parties to ensure quality submission documents for routine submissions
    • Troubleshoots issues found in components received and coordinates with responsible parties for clarification or revision
    • Builds and manages dossier structures in Lorenz Docubridge for global CMC submissions
    • Builds, compiles, and publishes eCTD submissions in-house using Veeva Vault RIM
    • Distributes, tracks, and archives non-eCTD submissions globally
    • Drafts eCTD content plans for CMC submissions
    • Independently prepares Cover Letters, FDA Forms, and submission content plans for routine maintenance and Investigational submissions
    • Performs submission verification on published submissions to confirm eCTD compliance
    • Maintains and updates submission tracking data in Verity (Veeva Vault) — planned, in-progress, and submitted submissions
    • Lead contact to ensure Literature References are correctly maintained in Verity (Veeva Vault)
    • Assists with translation document management activities
    • Supports process and system improvement initiatives (e.g., submission tracking tools, workflow enhancements)
    • Other miscellaneous regulatory operational activities as needed (e.g., US export waivers)

    Qualifications & Experience

    • BA/BS degree, science/technology field preferred
    • 6+ years relevant submissions and publishing experience

    Key Competency Requirements

    • Must have working knowledge of CMC/Quality dossier sections (e.g., Module 3 structure) to accurately compile and publish submission content
    • Foundational knowledge of global regulatory practices, electronic submission guidelines and requirements
    • Communicates questions and issues as they arise with possible solutions
    • Supports other functions as appropriate
    • Participates in submission team meetings
    • Effective written and verbal communication skills
    • Works with supervision
    • Ability to prioritize and strong attention to detail
    • Comfortable working with electronic docbases, databases, publishing systems, and eCTD viewers; technically savvy with Veeva Vault RIM, Lorenz Docubridge, Microsoft Office, and web-based applications

    We hire for skills and capabilities, not just credentials – if this role excites you, but doesn't perfectly match your resume, we encourage you to apply anyway.

    How We Work

    Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

    Supporting People With Disabilities

    BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [HIDDEN TEXT]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

    Candidate Rights

    BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

    For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

    Data Protection

    We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

    Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

    If this posting is missing required information required by local law or incorrect, contact BMS at [HIDDEN TEXT] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

    R1606855 : Submission Senior Specialist

    Sourced from foundit

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    Section · 02

    Skills

    VerityeCTD viewerselectronic docbasesmicrosoft officeDatabasesVeeva Vault RIMeCTD submissionsPublishing SystemsLorenz DocuBridge

    Section · Company

    About Bristol-Myers Squibb

    Bristol-Myers Squibb

    Bristol-Myers Squibb

    Pharma

    375

    employees

    1887

    139 years old

    New York

    United States

    ₹19.1L PA avg

    Avg at Bristol-Myers Squibb

    About

    We are a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. At Bristol Myers Squibb, we work every day to transform patients’ lives through science. We combine the agility of biotech with the reach and resources of an established pharmaceutical company to create a global leading biopharma company powered by talented individuals who drive scientific innovation. We have the brightest people in the industry and believe that their diverse experiences and perspectives help to bring out our best ideas, drive innovation and achieve transformative business results. Each day, our employees around the world work together for patients – patients are at the center of everything we do. They inspire us. They are the reason we come to work each day. We are proud of the advancements we have made in oncology, hematology, immunology, and cardiovascular disease, and we are dedicated to helping patients prevail over serious diseases through our diverse and promising pipeline and new scientific platforms. We are pursuing therapies at the forefront of scientific discovery with the goal of bringing an exciting new generation of life-changing treatments to patients. We aspire to be at the center of a vibrant healthcare innovation ecosystem, where academic research centers, biotech, and biopharma companies all contribute to continued scientific advancement.

    Industries

    PharmaBiotech & Life sciences

    Employee ratings

    10 reviews

    3.7/ 5

    Culture

    2.6

    Career growth

    2.2

    Work-life

    3.1

    Employees rate it well for

    Work-Life Balance38Compensation & Benefits37

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