Job Description

Working with Us
Challenging. Meaningful. Life-changing. Those aren\xe2\x80\x99t 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\xe2\x80\x99ll 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: .

Junior Veeva Test Specialist role is a member of the Veeva Drug Development & Cloud team and is accountable for Veeva Configuration Testing and Operational activities in the various vaults of the BMS Veeva ecosystem. In this role, the individual is primarily responsible for leading the testing efforts of Veeva product, enhancement, and operational releases across various functional areas.

If you want an exciting and rewarding career that is meaningful, consider joining our diverse team!

Desired Candidate Characteristics:

Have a strong commitment to a career in technology with a passion for healthcare

Ability to understand the needs of the business and commitment to deliver the best user experience and adoption

Able to collaborate across multiple teams

Excellent communication skills

Innovative and inquisitive nature to ask questions, offer bold ideas and challenge the status quo

Agility to learn new tools and processes

Key Responsibilities

Supporting a wide range of projects across multiple domain areas, selected candidate\xe2\x80\x99s responsibilities will include:

Collaborate closely with the Veeva Drug Dev & Quality Cloud team to obtain high level overview knowledge of the Veeva vault platform and various vaults

Assist in the development of Validation and test plans to aid deployment of the Veeva Vault Platform and general releases

Determine the ideal system operations and identify the types of tests and tools to use

Collaborate with QA to develop effective testing strategies, scenarios, and test plans

Work on all aspects of testing activities (unit, system, and/or user acceptance testing) of the

vault release including script generation, execution, review, and approval

Execute test cases (manual or automated) and document results and defects

Manage defects and effectively communicate with various stakeholders on testing status

Collaborate with engineering/development team to troubleshoot issues

Conduct post-release/post -implementation testing (Implementation Qualification and Operational/Production Qualification)

Work with cross-functional teams to ensure quality throughout the software development lifecycle

Deliver on validation documentation required on the various operational activities to ensure maintenance of the system\xe2\x80\x99s validated state

Qualifications & Experience

Requires thorough knowledge of the principles and concepts of a discipline and developed knowledge of other related disciplines, typically gained through a university degree and 2-3 years of experience. Works predominately within established procedures. Actively participates in troubleshooting of routine problems. Makes decisions that impact own work and other groups/teams. Works under minimal supervision.

Proven experience in testing or QA role

Experience in QA methodology and 21CFR Part 11 regulations

Experience in both test management and automated testing tools

Experience in life science industry with Drug Development life cycle knowledge

Identifies opportunities to improve and grow, balancing performance feedback and career development

Applies a continuous improvement mindset in enhancing efficiency, quality and effectiveness or their work outputs.

Ideal candidate will also have GxP/GMP experience and testing certification

If you come across a role that intrigues you but doesn\xe2\x80\x99t 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 \xe2\x80\x9cTransforming patients\xe2\x80\x99 lives through science\xe2\x84\xa2 \xe2\x80\x9d, 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.

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 . Visit 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.

Bristol-Myers Squibb