Global Regulatory Sciences Lead

6 days ago


Hyderabad, Telangana, India Bristol Myers Squibb Full time

Transforming Patients' Lives through Science

The CMC Regulatory Associate Director, Biologics plays a pivotal role in developing, compiling, and reviewing the Quality Module for regulatory submissions related to biologics products, encompassing clinical trial applications, new marketing applications, HA responses, and background packages. As the primary interface between Global Regulatory Sciences (GRS) and Global Product and Supply (GPS), this role assesses manufacturing change controls for global impact and guides technical teams on practical aspects of global change management.

Uniquely Interesting Work, Life-changing Careers

At Bristol Myers Squibb, every employee contributes to work that goes beyond the ordinary, driven by a shared vision of transforming patients' lives through science. An inclusive culture promotes diversity in clinical trials, and our values of passion, innovation, urgency, accountability, inclusion, and integrity bring out the best in our colleagues.

On-site Protocol

Bristol Myers Squibb employs a diverse occupancy structure, determining where employees conduct their work. This structure includes site-essential, site-by-design, field-based, and remote-by-design jobs. The assigned occupancy type depends on the role's nature and responsibilities.

Workplace Inclusion and Support

Bristol Myers Squibb is dedicated to ensuring that employees with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations, and ongoing support. Applicants can request accommodations before accepting a job offer, and the company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.



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