Associate Director, Drug Product Analytical Science and Technology

Associate Director, Drug Product Analytical Science and Technology Position Summary of this leadership role is the technical oversight of the analytical method lifecycle within the Cell Therapy Analytical Science and Technology organization. The Associate Director leads a team of scientists providing analytical subject‑matter expertise to the Commercial Quality Control organization during investigations, commercial drug product method validation and transfers, regulatory submissions and Health Authority interactions. Additional responsibilities include overseeing operational workflows, metrics, and quality events such as actions and investigations. Duties & Responsibilities Lead and manage a team of analytical Subject‑Matter Experts (SME) responsible for the commercial drug product release methods used in cellular biology, molecular, and flow cytometry areas. Provide technical oversight and guidance to the team for method performance troubleshooting, evaluation of analytical test methods, and data generated by internal and external laboratories, including investigations related to out‑of‑specification, out‑of‑trend, and aberrant results. Oversee method performance metrics and the team’s completion of quality events, including actions and investigations, within electronic systems. Act as an SME in functional areas as needed. Partner with analytical development and the Commercial QC organization to identify method optimization and automation opportunities to enhance productivity and reduce testing costs. Interface with analytical development functions on method qualification strategies. Hire, mentor, and develop exceptional ASAT personnel. Qualifications Bachelor’s degree in a relevant scientific discipline or equivalent is required; an advanced degree is preferred. 10+ years of relevant experience or the equivalent combination of education and experience, preferably in a regulated environment (GMP), cellular therapy or gene therapy, with 2+ years’ experience in Analytical Science. 5+ years of leadership experience. Experience in the analytical method lifecycle, including method transfer, validation, and maintenance. Advanced knowledge and implementation of Quality Management including SOPs, Change Controls, Deviations, CAPAs, Risk Assessments and data integrity principles. Advanced understanding of regulatory requirements and guidelines related to the manufacture of cell therapy products (FDA, EMA, ICH, USP, EP). Self‑directed with a high degree of professional integrity, highly organized, and detail oriented. Ability to work independently and to collaborate cross‑functionally to drive operational and quality excellence. Demonstrated leadership and management skills, including establishing strategic direction and goals, and guiding execution while fostering a team‑based environment. Advanced verbal and written communication skills with the ability to tailor style for a variety of audiences, including the ability to author general, technical, and complex business documents. Advanced mentoring, coaching, influencing, negotiating, and personal interaction skills. Ability to travel to other BMS sites or Partner sites as required. Compensation Overview The starting compensation range for this role varies by location and position type: Devens, MA – $168,930 – $204,702 Seattle, WA – $173,660 – $210,439 Summit West, NJ – $157,880 – $191,312 In addition to base salary, the role may be eligible for incentive cash and stock opportunities. Final individual compensation is determined based on demonstrated experience and performance. Benefits Health Coverage: Medical, pharmacy, dental, and vision care. Well‑being Support: Programs such as the BMS Well‑Being Account, BMS Living Life Better, and Employee Assistance Programs. Financial Well‑being & Protection: 401(k) plan, short‑ and long‑term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. Work‑life Benefits: Paid Time Off, unlimited paid sick time (where applicable), paid volunteer days, summer hour flexibility (where eligible), leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs, and an annual global shutdown. Equal Employment Opportunity Statement We are dedicated to providing a workplace that values diversity and inclusion. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. #J-18808-Ljbffr Bristol-Myers Squibb