Sr. Specialist, Quality Control Raw Materials (Method Transfer/Validation)

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. Responsibilities Perform method transfer, validation, verification and routine testing of materials; lead retain sample management activities. Anticipate and perform routine troubleshooting and problem solving with minimal guidance. Perform data verification, data review and review of GMP documentation for general and complex methods. Perform document revision, project, CAPA and deviation/investigation related tasks and/or continuous improvement efforts. Train and mentor others on QC test methods, processes, and procedures. Perform other tasks as assigned. Specific Knowledge, Skills, Abilities Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements. Demonstrated technical writing skills. High problem‑solving ability/mentality, technically adept and logical. Ability to communicate effectively with peers, department management and cross‑functional peers about task status, roadblocks and needs. Ability to work in a fast‑paced team environment, meet deadlines, and prioritize work. Advanced knowledge of LIMS and laboratory data analysis systems preferred. Education / Experience / Licenses / Certifications Bachelor’s degree or equivalent required, preferably in science. Advanced degree preferred. Compensation Overview Summit West – NJ – US $82,220 – $99,632 (starting range for a full‑time employee). Additional incentive cash and stock opportunities, based on eligibility, may be available. Final, individual compensation will be decided based on demonstrated experience. Benefits Health Coverage – Medical, pharmacy, dental, and vision care. Well‑being Support Programs such as BMS Well‑Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). Financial Well‑being and 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 US Exempt Employees flexible time off (unlimited, with manager approval, 11 paid national holidays). Phoenix, AZ, Puerto Rico and Rayzebio exempt/non‑exempt/hourly employees 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays. Eligible employees may have additional time off: unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs, and an annual Global Shutdown between Christmas and New Years Day. On‑site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. Site‑essential roles require 100% onsite; site‑by‑design roles may be eligible for a hybrid model with at least 50% onsite. Field‑based and remote‑by‑design roles require essential physical presence to attend meetings and collaborate. Candidate Rights BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws. Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Position Details R1603007 – Sr. Specialist, Quality Control Raw Materials (Method Transfer/Validation) #J-18808-Ljbffr Bristol Myers Squibb