Working with UsChallenging. 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: careers.bms.com/working-with-us.
BMS Hyderabad is an integrated global hub where our work is focused on helping patients prevail over serious diseases by building sustainable and innovative solutions. This important science, technology, and innovation center will support a range of technology and drug development activities that will help us usher in the next wave of innovation.
Key ResponsibilitiesPerforms EVMPD maintenance coordination through data entry and data QC for EVMPD
Maintains understanding of the assigned EVMPD Processes
Manages daily workload and independently addresses questions for assigned regulatory processes
Contributes to enhancements in developed areas of expertise
Provides support for internal audits, HA inspections and corrective action plans.
Supports management in developed areas of expertise
Recognizes and reports data compliance issues and how they impact assigned processes
Executes operational aspects of enabled processes according to BMS procedures
Create, update and/or execute new reports in RIM system for any new data entries or updates to existing product data
Collaborate with stakeholders and SMEs to find solutions and rectify any ongoing or potential issues, as needed
Develop working knowledge of global regulatory practices and requirements as they pertain to IDMP and EVMPD
Recognizes and reports data compliance issues, and able to derive how they impact assigned processes and other processes
Experience with the life cycle of marketed products (preferred, but drug development experience will also be considered) processes.
Solid regulatory knowledge and previous experience in the Regulatory Information Management area
Demonstrate experience and understanding of the procedures and decision-making process of Health Authorities as it relates to RIM.
Clear knowledge and experience with EVMPD, IDMP, and/or SPOR.
Possesses knowledge in standard desktop applications and RIM systems, including effective troubleshooting skills.
Easily adapts to new software and procedures.
Strong attention to detail.
Excellent command of English language, written and oral.
Demonstrated ability to follow specific standards and processes and ability to identify when others do not.
Qualifications & ExperienceBA/BS degree, science / technology field preferred
3-5 years of pharmaceutical experience
Experience with the life cycle of marketed products (preferred, but drug development experience will also be considered) processes.
Solid regulatory knowledge and previous experience in the Regulatory Information Management area
Demonstrate experience and understanding of the procedures and decision-making process of Health Authorities as it relates to RIM.
Clear knowledge and experience with EVMPD
Possesses knowledge in standard desktop applications and RIM systems, including effective troubleshooting skills.
Easily adapts to new software and procedures.
Strong attention to detail.
Demonstrated ability to follow specific and standards and processes.
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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 CareersWith 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 ProtocolPhysical 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.
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 [Confidential Information]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
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.
