ExM Bio/Sterile Quality Operation Manager

at  BristolMyers Squibb

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 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.

REQUIRED QUALIFICATION(S) AND DESIRED EXPERIENCE

• Minimum B.S. degree in relevant scientific discipline e.g. Biochemistry, Microbiology, Pharmacy, Biological Sciences or Related Pharmaceutical Science
• Minimum of four (4) years’ experience in pharmaceutical operations at the manufacturing site
• At least two (2) years in Quality, ideally in product release or pharma project quality
• Experience in aseptic, sterile and biological drug product manufacturing
• Experience in contract manufacturing or contract testing
• Experience with technical writing, ideally authoring investigations, quality risk assessments, process descriptions, or study protocols
• Ability to negotiate and clearly present complex topics both in written and verbally
• Knowledge of combination products manufacturing or finished drug product packaging
• Experience with biological product testing methods/quality control
• Experience with Good Manufacturing Practice (GMP) tools and standard applications: SAP, Quality Management System (QMS) or Verity, Microsoft Office (especially OneNote and Visio)
  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.

• Perform product disposition activities to ensure timely supply of drug substance, drug product, and finished product that meet commercial customer requirements while ensuring compliance with testing standards, standard operating procedures (SOPs), validation guidelines and regulatory filings
• Author, compile and maintain documentation needed for disposition of the product from Contract Manufacturing Organizations (CMOs)
• Review disposition documentation from CMOs and recommend disposition, escalating potential issues
• Ensure batch documentation relative to CMO materials and products is maintained and archived
• Input required deviation, complaint, change control, and product disposition information into applicable enterprise systems
• Prepare and review of Quality Agreements with external manufacturers and external laboratories
• Manage and report quality metrics in relation to CMO performance
• Prepare and review Annual Product Quality Reviews for BMS products at CMOs as required
• Work with CMOs and BMS project teams to ensure pre-approval inspection (PAI) readiness and filing submission readiness for the new products transferred to CMOs or major process changes.
• Assist with reviewing analytical and method protocols and reports for compliance
• Assist with commercialization quality-related activities on the new products transferred or launched to/from CMOs
• Provide quality support during self-inspections, internal audits, and regulatory agency inspections at contract manufacturers.
• Support supplier relationship manager, global procurement, supply chain and manufacturing science and technology teams for new projects, technical transfers programs, supplier selection programs, and commercial manufacturing activities
• Review validation documents, deviations, and change controls and escalate any potential compliance gaps
• Escalate issues to senior management to ensure that issues are resolved to support BMS business and compliance requirements
• Evaluate external quality complaint investigations provided by CMOs
• Ensure maintenance of System, Applications and Products (SAP) Master Data (related to Quality)