Project Engineer

BMS is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose is to discover and develop therapies that will change the course of human health. We value the passion for patients, quest for innovation, spirit of independence, and love of challenge. With a presence in more than 70 countries, we develop novel cellular immunotherapies based on two complementary platforms: Chimeric Antigen Receptors (CARs) and T Cell Receptors (TCRs). Our goal is to revolutionize medicine by re-engaging the body's immune system to treat cancer.Project Engineer – Materials Science (CTTO)We are seeking a Project Engineer to support the Material Review Committee (MRC) within the Cell Therapy Technical Operations (CTTO) department. The role drives dual sourcing, alternate sourcing, and business-continuity mitigation projects, with accountability for global and site implementation change management. It includes vendor management, change control partnership, proactive process monitoring, deviation management, and process improvements to support CAR-T therapies during late-stage clinical, tech transfer, and commercial production.Responsibilities (not limited to)Execute MRC-prioritized material risk mitigation projects, including dual sourcing, alternate sourcing, and business-continuity initiatives for raw materials and single-use systems.Own global and site implementation change controls, coordinating BOM updates, master data changes, and site execution activities.Collaborate with MRC to translate risk-prioritized materials into aligned mitigation strategies and executable project plans.Coordinate cross-functional execution with CTTO Labs, Supplier Quality, Supply Chain Planning, and site functions to support lab studies, PPQ, stability, and implementation activities.Track project milestones, risks, and dependencies; escalated execution risks and resource constraints to the MRC Lead and Sponsors as needed.Ensure alignment with GMP, quality, and documentation requirements throughout project execution and site implementation.EducationRequired B.S. with 4 years of experience or M.S. with 1 year of relevant experience in Chemical, Biochemical, Biomedical Engineering, Materials Science, or a related discipline, or equivalent experience.Skills / Knowledge RequiredExperience executing cross-functional projects in a biopharmaceutical GMP manufacturing environment.Experience with technical and/or manufacturing support for biologics or cell therapy clinical or commercial manufacturing operations.Demonstrated ability to lead cross-functional project execution across global and site teams.Working knowledge of change control processes, including site implementation actions, BOM updates, and master data impacts.Strong organizational, communication, and stakeholder management skills with the ability to drive execution under tight timelines.Experience collaborating with external suppliers is a plus.Experience with pharmaceutical single-use systems, consumables, and raw materials (e.g., design, testing, or manufacturing) is a plus.50% onsite required.Work Schedule: Mon-Fri (normal business hours).Contract Assignment InformationThis posting is for a contract assignment with ASK Staffing DBA ASK Consulting to provide services to Bristol Myers Squibb. The starting hourly compensation is $56–$58.43/hr. Final compensation and available benefits will be determined by ASK Staffing, Inc.About ASK ConsultingASK Consulting is an award-winning, woman-owned staffing and recruitment solutions provider with over three decades of industry experience. We specialize in connecting businesses of all sizes across IT, healthcare, engineering, finance, and more with top-tier professionals.BenefitsASK Consulting provides ACA-compliant health coverage, dental, vision, short- and long-term disability for eligible employees, commuter benefits, a 401(k) plan (no matching), and a referral bonus program. Unpaid leave and paid sick leave are offered as required by law.Equal Opportunity EmployerASK Consulting is an equal opportunity employer and does not discriminate based on race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability, veteran status, or any other protected classification.California Applicant NoticeASK Consulting complies with the California Privacy Rights Act (CPRA) and relevant privacy laws. For more information, review our Notice to California Job Applicants regarding the Collection of Personal Information.Fair Chance Employment NoticeBackground checks may be required. We consider qualified applicants with arrest or conviction records per applicable ordinances.Applicants must be legally authorized to work in the United States and should not submit false information. The posting does not constitute an offer of employment, and any eventual offer will be at will.J-18808-Ljbffr