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Senior Specialist - Regulatory Submissions

salary Not Disclosed
company-logo
job companyBristol-myers Squibb India Private Limited
job location Suraram, Hyderabad
job experience6 - 6+ years Experience in Nurse / Compounder
1 Opening
full_time Full Time

Job Highlights

qualification
All Education levels
gender
All genders
jobShift
5 days working | Day Shift

Job Description

Submission Senior Specialist 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 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 Experience Level Senior Level

Other Details

  • It is a Full Time Nurse / Compounder job for candidates with 6 - 6+ years Experience.

More about this Senior Specialist - Regulatory Submissions job

  1. Who is eligible to apply for this Senior Specialist - Regulatory Submissions job at Bristol-myers Squibb India Private Limited?
    Ans : Candidates should have All Education levels for this Senior Specialist - Regulatory Submissions job offered by Bristol-myers Squibb India Private Limited.
  2. How much can you earn in this position?
    Ans : Salary details will be shared during the hiring process.
  3. What shift and timings does this job follow?
    Ans : This Senior Specialist - Regulatory Submissions job follows a Day shift.
  4. Do you need to visit the office for this job?
    Ans : Yes, candidates need to visit the office and work from the location in Suraram, Hyderabad.
  5. How many vacancies are there for this Senior Specialist - Regulatory Submissions job?
    Ans : There is 1 vacancy for this Senior Specialist - Regulatory Submissions role.
  6. Is this job open for all genders?
    Ans : Yes, this Senior Specialist - Regulatory Submissions job is open for both male and female candidates.
  7. What is the job location for this position?
    Ans : The job location for this Senior Specialist - Regulatory Submissions position is Suraram, Hyderabad.
  8. What makes this Senior Specialist - Regulatory Submissions job a good opportunity?
    Ans : The employer has not disclosed the salary for this role, but it is a Full Time opportunity with 1 opening.
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Contact Person

BRISTOL-MYERS SQUIBB INDIA PRIVATE LIMITED
Posted 5 hours ago
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