Bristol Myers Squibb

Bristol Myers Squibb

Posted via Workday

Submission Senior Specialist

Apply by Oct 4, 2026

Posted Sep 28, 2026

Role at a glance

Job function
Legal & Compliance Compliance & Regulatory Affairs
Salary
Not Disclosed
Location
TS, Indiana, United States
Employment
Full-time
Experience
6+ years relevant submissions and publishing experience
Education
BA/BS degree, science/technology field preferred

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Role Summary

AI-generated

The Submission Senior Specialist supports routine and investigational regulatory submissions, including CMC submissions, for Health Authorities. The role manages submission components, publishing, verification, tracking, and related document activities.

What You'll Do

  • Tracks, collects, and reviews components for routine Health Authority submissions, coordinating with responsible parties to resolve...
  • Builds and manages dossier structures and compiles and publishes eCTD submissions using Lorenz Docubridge and Veeva Vault RIM.
  • Distributes, tracks, and archives global non-eCTD submissions; drafts eCTD content plans and prepares cover letters, FDA forms, and...
  • Verifies published submissions for eCTD compliance and maintains submission tracking data in Verity (Veeva Vault), including literature...
  • Assists with translation document management and supports process and system improvement initiatives and other regulatory operations...

Generated from the employer's posting. Verify important details before applying.

View full posting

Qualifications

6+ years of relevant submissions and publishing experience. Working knowledge of CMC/Quality dossier sections, including Module 3 structure; foundational knowledge of global regulatory practices and electronic submission guidelines and requirements. Comfortable with electronic docbases, databases, publishing systems, and eCTD viewers; technically savvy with Veeva Vault RIM, Lorenz Docubridge, Microsoft Office, and web-based applications. Effective written and verbal communication, prioritization, attention to detail, and ability to work with supervision.

Preferred

  • BA/BS degree in a science/technology field.

Original job description

Content provided by the employer

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 [email protected]. 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 [email protected] 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
Bristol Myers Squibb

About the company

Bristol Myers Squibb

Large Enterprise

Bristol Myers Squibb is a global biopharmaceutical company committed to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a focus on oncology, immunology, and cardiovascular health, the company leverages advanced science and technology to create transformative therapies that address critical unmet medical needs. Operating in more than 70 countries, Bristol Myers Squibb emphasizes collaborative efforts and strong partnerships in research and development to drive advancements in healthcare and improve patient outcomes worldwide.