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.
Key Responsibilities
Functional and Technical
Participate in CSV activities for applications across multiple GxP business areas to ensure 'fit for use' before release to production setting. Participate in Qualification activities as it relates to infrastructure applications and hardware in a timely manner. Be part of the team that Conducts risk & impact assessments to determine the extent of validation and qualification requirements.
Implementation of organizational IT controls in accordance with applicable regulations and internal procedures. Author CSV deliverables including but not limited to Plans & Summary Reports. Support the SLC process as it relates to application validation and infrastructure qualification. Identifies opportunities for simplification, automation for CSV activities and partners with IT Delivery teams and IT Quality to implement. Supports inspections and audits (internal and external). Conducts periodic reviews to ensure applications remain in a state of compliance. Participates and represents IT Validation Services in problem management and audit remediation activities. Provides regular status updates to one up manager and escalates any potential issues in a timely manner People Management:
Support CSV staff across defined GxP business unit applications to ensure 'fit for use' before release to production environment Qualifications & Experience
B.E./B.Tech. or