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Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Senior Manager, IT - Digital Plant Applications & Infrastructure

System Administration +1Confirmed live in the last 24 hours
Full-timeIndianapolis, IN, USAIn-person

About the Job

Requirements

  • A bachelor's degree in Engineering, Information Technology, or a Science field, or equivalent experience.
  • Seven to ten or more years of Information Technology experience in biotechnology, pharmaceuticals, life sciences, or Good Practice (GxP) manufacturing.
  • Proven technical leadership and management experience.
  • Demonstrated experience implementing automation and digitization projects.
  • A Bachelor of Science or Master of Science degree in Information Technology or a similar degree, or equivalent experience.
  • Knowledge of pharmaceutical Information Technology architecture and infrastructure, including networks, servers, human-machine interfaces, printers, scanners, switches, firewall rules, and domains.
  • Knowledge of cGMP, GxP, GAMP, Software Development Life Cycle regulations, including 21 CFR Part 11, and good documentation practices.
  • Knowledge of pharmaceutical, manufacturing, and laboratory systems and equipment that support biologics and clinical manufacturing.
  • Knowledge of cybersecurity, patching, and Information Technology life cycle management.
  • Understanding of computer system validation.
  • Ability to apply artificial intelligence to improve team execution and decision-making.
  • Ability to wear personal protective equipment as required and to work comfortably with radioactive materials.

Responsibilities

  • Implement RayzeBio's growth vision and lead efforts to enable digital processes that support site commercialization objectives.
  • Ensure digital systems applications and computer system validation for laboratory and process automation are enabled and maintained to support radiopharmaceutical technologies.
  • Work with laboratory and process automation, corporate systems, small-biotech systems, and functions across the Whitestown site.
  • Work with architectural and Information Technology partners and specialty equipment manufacturers to achieve technology and commercialization goals.
  • Maintain continuous operation of Information Technology and data for laboratory and process automation systems, including manufacturing execution systems, laboratory information management systems, local manufacturing systems, quality control and quality management site systems, and associated site infrastructure.
  • Partner with Engineering in the process automation space.
  • Deliver site service-level management scope and processes with Information Technology groups or vendor-managed services, including service-level agreements and disaster recovery/service continuity.
  • Work with service providers to deliver effective, innovative, and stable solutions that meet site needs.
  • Support site regulatory inspection readiness and data integrity initiatives.
  • Partner on new demands from Manufacturing Operations, Quality, Supply Chain, and Manufacturing Science & Technology.
  • Identify key technology trends and assess how new technologies can provide improved solutions for the manufacturing site.
  • Support deployment of long-term, three-year roadmaps identifying organizational capabilities with the greatest business impact, partnering and benchmarking with external sources.

Desired Qualifications

  • Prior radiopharmaceutical experience is highly valued but not required.

About the Company

Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Bristol Myers Squibb discovers, develops and sells prescription medicines for serious illnesses, including cancer, blood disorders, immune diseases and heart disease, for patients treated by doctors and hospitals around the world. Its best-known drug is Opdivo, an immunotherapy that helps the body's own immune system find and attack many kinds of cancer. Researchers develop drug candidates in its labs or bring them in through acquisitions and partnerships, then test them in clinical trials to win regulatory approval. The company makes and markets the approved medicines and earns its revenue from sales of patent-protected drugs. Its roots go back to a business founded in 1887, and it is based in Lawrence Township, New Jersey.

Company size
10,001+
Company stage
IPO
Headquarters
Lawrence Township, NJ
Founded
1887

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