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Bristol Myers Squibb

Director, Cell Therapy Drug Product Operations Risk Management

Bristol Myers Squibb, Harvard, Massachusetts, us, 01451

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Director, Cell Therapy Drug Product Operations Risk Management

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Bristol Myers Squibb

Position Summary The Director, Cell Therapy Drug Product Operations Risk Management is responsible for delivering improvements in commercial cell therapy product supply reliability by leading risk assessments, prioritizing risk mitigations, and managing the resulting project portfolio. The scope encompasses suppliers, process and analytics across the DPO manufacturing network. As a key member of the Proactive Risk Management team, this role partners cross‑functionally to holistically assess and mitigate risks to supply reliability.

Key Responsibilities

Assess risks/vulnerabilities that impact our ability to reliably supply product on‑time and in‑spec to patients, covering Suppliers, Process, and Analytical functions.

Create a holistic Risk Register capturing the landscape of risks and mitigation projects, ensuring alignment with Business Continuity Management & Quality Risk Management.

Prioritize a selection of risk mitigation projects and identify opportunities to accelerate.

Partner with matrix team leads to build project schedules, charters, budgets, and resourcing plans.

Identify areas for deeper dive risk assessment and systems/processes to target for improvement; develop plans to address.

Foster a culture of accountability, inclusion, integrity, and innovation.

Qualifications & Experience

B.S., M.S., or Ph.D. in Chemical Engineering, Biochemical Engineering, Biochemistry, or a related discipline with 15+ years (B.S./M.S.) or 12+ years (Ph.D.) of experience in biologics or cell therapy process development, analytical development, tech transfer, and/or GMP manufacturing support.

Strong understanding of CMC regulatory requirements, DS & DP manufacturing, and analytical testing.

Excellent strategic thinking, problem‑solving, decision‑making, and communication skills.

Strong knowledge of ICH guidelines, control strategies, and validation lifecycle frameworks.

Ability to effectively utilize project management and Lean Six Sigma tools is a plus.

Excellent interpersonal, collaborative, team‑building, and communication skills.

Ability to influence senior stakeholders and align cross‑functional teams on complex technical and strategic issues.

Approximately 10‑20% travel.

Compensation Overview Bothell – WA – US: $209,070 – $253,339 Devens – MA – US: $209,070 – $253,339 Summit West – NJ – US: $190,060 – $230,308

Additional incentive cash and stock opportunities (based on eligibility) may be available. Final individual compensation will be determined based on demonstrated experience.

Benefits Medical, pharmacy, dental and vision care; Wellbeing support; 401(k); Paid vacation and holiday programs; Parental, caregiver, bereavement and military leave; Tuition reimbursement and recognition programs; Work‑life flexibility and hybrid work options where eligible.

EEO Statement Bristol Myers Squibb is an equal opportunity employer. We encourage applications from a diverse workforce and provide reasonable accommodations for qualified candidates with disabilities. Visit careers.bms.com/eeo–accessibility for our full Equal Employment Opportunity statement.

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