Submission Senior Specialist

Bristol Myers Squibb · Hyderabad

  • Experience6–7 yrs
  • SalaryNot disclosed
  • Work modeonsite
  • Posted28 Sept 2026

About Bristol Myers Squibb

Bristol Myers Squibb is hiring in Hyderabad in pharma biotech. This role looks for around 6+ years of experience.

Skills

  • CMC submissions
  • Veeva Vault RIM
  • Lorenz Docubridge
  • eCTD
  • global regulatory practices
  • electronic submission guidelines
  • Microsoft Office

The role

A submission specialist at a pharmaceutical company compiles regulatory dossiers and manages CMC submissions using Veeva Vault RIM and Lorenz Docubridge. The role also applies eCTD compliance and global regulatory practices to maintain submission content and tracking.

Full job description

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 AuthoritiesInteracts with responsible parties to ensure quality submission documents for routine submissionsTroubleshoots issues found in components received and coordinates with responsible parties for clarification or revisionBuilds and manages dossier structures in Lorenz Docubridge for global CMC submissionsBuilds, compiles, and publishes eCTD submissions in-house using Veeva Vault RIMDistributes, tracks, and archives non-eCTD submissions globallyDrafts eCTD content plans for CMC submissionsIndependently prepares Cover Letters, FDA Forms, and submission content plans for routine maintenance and Investigational submissionsPerforms submission verification on published submissions to confirm eCTD complianceMaintains and updates submission tracking data in Verity (Veeva Vault) — planned, in-progress, and submitted submissionsLead contact to ensure Literature References are correctly maintained in Verity (Veeva Vault)Assists with translation document management activitiesSupports 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 preferred6+ 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 contentFoundational knowledge of global regulatory practices, electronic submission guidelines and requirementsCommunicates questions and issues as they arise with possible solutionsSupports other functions as appropriateParticipates in submission team meetingsEffective written and verbal communication skillsWorks with supervisionAbility to prioritize and strong attention to detailComfortable 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 adastaffingsupport@bms.com. 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 TAEnablement@bms.com 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