Software Engineer I- Veeva Quality

The Software Engineer I - Veeva Quality role at Bristol Myers Squibb is part of the Veeva Drug Development & Cloud team. This position is responsible for Veeva configuration and operational activities across the BMS Veeva ecosystem, including supporting platform updates, enhancements, end-user support, and access management. The role involves architecture, design, and testing, with a focus on delivering the best user experience and maintaining system validation. Candidates should have a passion for healthcare technology and strong collaboration skills.

Must Have

• Minimum 4-6 years of experience in Veeva
• Thorough knowledge of principles and concepts of a discipline (e.g., software engineering/IT)
• Experience in implementing/supporting SaaS (Software as a Service) solutions
• Experience in automated testing tools
• Experience in life science industry with Quality domain knowledge
• Experience in GMP (Good Manufacturing Practice) Practices
• Ability to collaborate across multiple teams
• Excellent communication skills
• Agility to learn new tools and processes
• Accountable for Veeva Configuration and Operational activities
• Assist in deployment of Veeva Vault Platform and general releases
• Perform system analysis, design, and configuration to meet business requirements
• Contribute to all aspects of testing activities (unit, system, and/or user acceptance testing)
• Deliver on validation documentation required to ensure maintenance of the system’s validated state
• Provide operational support activities of the Veeva vaults to global user community
• Perform periodic user access review of the applications

Good to Have

• Familiarity with Java SDK
• Veeva Associate Administrator Level (previously called Veeva White Belt) certification
• Innovative and inquisitive nature to ask questions, offer bold ideas and challenge the status quo

Perks & Benefits

• Benefits and Wellbeing
• Recognition
• Time Off
• Health Benefits
• 8 People & Business Resource Groups

Life at BMS

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. 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.

Software Engineer I - Veeva Quality role is a member of the Veeva Drug Development & Cloud team and is accountable for Veeva Configuration and Operational activities in the various vaults of the BMS Veeva ecosystem. In this role, the individual is primarily responsible for supporting platform updates, enhancements and/or end-user support & access management activities including Architecture, design, and testing. 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’s 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 deployment of the Veeva Vault Platform and general releases including documentation and testing.
• System analysis, design, and configuration to meet business requirements.
• Contribute to all aspects of testing activities (unit, system, and/or user acceptance testing) of the vault release including script generation, execution, review, and approval. Deliver on validation documentation required on the various operational activities to ensure maintenance of the system’s validated state.
• Provide operational support activities of the Veeva vaults to our global user community, such as maintenance and break-fix releases, security assessments, regulatory risk assessments, incident response, etc.
• Perform periodic user access review of the applications.
• Obtain/maintain a Veeva Associate Administrator Level certification.

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.
• Minimum 4-6 years of experience in Veeva.
• Familiarity with Java SDK is a plus.
• Works within established procedures and actively participates in troubleshooting of routine problems. Makes decisions that impact own work and other groups/teams.
• Works under minimal supervision. Experience in implementing/supporting SaaS (Software as a Service) solutions
• Experience in automated testing tools
• Experience in life science industry with Quality domain knowledge
• Experience in GMP (Good Manufacturing Practice) Practices
• 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.
• Able to review multiple factors of data and can effectively organize information to compare and assess short and long-term implications. Can create a well-developed recommendation and sound actions.
• Ideal candidate will also have Veeva Associate Administrator Level (previously called Veeva White Belt) certification.

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 a supportive culture, promoting global participation 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

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

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

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.