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Job Details

Bristol Myers Squibb

US Labeling Specialist

Equipment/Technology Specialist

Equipment and Facilities Specialist


Tampa, Florida, United States

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more:

Ideal Candidate:
  • Bachelor’s or Master’s degree, preferred in sciences with > 2 years of labeling experience in a regulated environment, or > 3 years other pharmaceutical experience
  • Must possess an excellent command of English language
  • Good understanding of pharmaceutical or medical terminology
  • Good communication and organizational skills and a meticulous eye for details
  • Proficiency in standard office technology, including Microsoft Suite, Outlook Mail/Calendar; willing to learn additional applications as needed
  • Experience working on multi-disciplinary teams and projects
  • Good knowledge of rigorous pharmaceutical and/or scientific documentation practices and change control processes (e.g. revision control)


  • Works under the guidance of the US Labeling Operations Senior Manager or with Senior Specialists
  • Manages external requests for data with professionalism and adherence to policy and regulations.
  • Prepares and distributes US labeling submission documents that meet FDA and BMS internal standards (including annual reports, xml and eCTD documentation).
  • Manages the end-to-end labeling process to minimize the risk and associated costs to BMS and patients of a significant error occurring in final labeling preparations that results in a product delay or recall due to labeling;
  • Approves and maintains artwork for US packaging components including decision when artwork should be printed “at risk.”
  • Collaborates with contributing functional areas and external sources to verify accuracy of submission labeling components in the required formats. Advises Global Manufacturing and Supply of upcoming changes to labeling and providesguidance on when changes need to be implemented in the market; This responsibility encompasses safety and quality labeling compliance
  • Proactively identifies risks and issues, and develops solutions to challenging areas related to assigned projects in the interest of keeping projects streamlined and moving forward.

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

COVID-19 Information
To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.

BMS is dedicated to ensuring that people with disabilities can perform complex functions through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or in any part of the recruitment process, direct your inquiries to Visit to access our complete Equal Employment Opportunity statement.

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

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