Jobs and Careers
BR

Senior Director, Analytical Excellence

Bristol Myers Squibb
United Statesfull_timeVerifiedPosted 6 Jan 2026
💰 $287,710/yr($230,950/yr$287,710/yr)

About the role

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.

Position Summary

The Sr. Director, Analytical Science and Technology (ASAT) Analytical Excellence is responsible for defining and driving strategic Quality Control (QC) Excellence programs across BMS’s global cell therapy network. This role will be responsible for driving alignment and harmonization of analytical method performance, execution, and efficiency improvements, partnering closely with QC, Quality, and Analytical Development stakeholders. The individual will champion initiatives that improve analytical method performance, facilitate best-in-class operational practices, and optimize the use of analytical instruments and software platforms.

Duties/Responsibilities

  • Develop, implement, and continuously improve the QC Excellence strategy for global QC sites, focusing on method harmonization, performance optimization, and operational efficacy

  • Lead cross-functional teams to establish standardized procedures, tools, and metrics for routine QC testing

  • Partner with site QC, Quality (GPQ and QA), and ASAT functions to assess current practices, identify gaps, and drive alignment

  • Champion data-driven decision-making and continuous improvement principles for analytical method execution

  • Own and evolve business processes for QC-related analytical instruments and software systems, coordinating with IT and site SMEs

  • Benchmark industry best practices and implement innovative approaches to process efficiency, regulatory compliance, and quality improvement

  • Monitor performance indicators, compliance metrics, and operational dashboards, using findings to inform global improvement initiatives

  • Prepare and present strategic plans, performance updates, and improvement proposals to executive leadership

  • Mentor and develop team members, fostering a high-performance and collaborative culture

  • Ensure robust change management and stakeholder engagement throughout all initiatives

  • Foster a culture of excellence and accountability for cell therapy across all partners and stakeholder.

Reporting Relationship

Reports to the Executive Director, Analytical Science and Technology

 Specific Knowledge, Skills, Abilities:

  • Extensive experience in analytical science, QC operations, or method lifecycle management within the pharmaceutical/biologics industry; leadership at a multi-site/global level preferred

  • Demonstrated expertise in analytical method development, validation, transfer, troubleshooting, and routine QC operations

  • Proven track record of leading complex, cross-functional global initiatives, preferably in operational excellence or continuous improvement roles

  • Deep understanding of analytical instrument platforms and enterprise software systems used in QC testing

  • Strong project management and organizational skills, able to coordinate multiple initiatives across diverse stakeholders

  • Exceptional communication, influencing, and stakeholder engagement abilities

  • Data analytics competence, with ability to analyze complex data sets and drive improvement actions

  • Sound knowledge of current GMP, regulatory expectations, and quality management systems

  • Change management expertise, with experience implementing harmonization or transformation programs at scale

  • Collaborative leadership style; ability to inspire and drive teams towards a common vision

  • Strategic thinker with a results-driven, proactive approach

  • Demonst

Apply for this role

Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.

Apply Now →Generate Application Kit

Free account required — sign up in 30s

Company

Bristol Myers Squibb

View company profile →