Manufacturing Associate, Liso-cel CAR-T, Manufacturing Operations

Career Areas Career Stories Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Careers Home Life at BMS Career Areas Student Opportunities Events How We Recruit Career Stories Search this site Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Single PositionView All JobsManufacturing Associate, Liso-cel CAR-T, Manufacturing OperationsSummit West - NJ - US No longer accepting applications.Job IDR1603700Date posted06/18/2026DepartmentCell TherapyManufacturing AssociateBiopharmaceutical Manufacturing | Day Shift (Quad 1) | cGMP Cleanroom EnvironmentAbout the RoleThe Manufacturing Associate is responsible for producing human blood-derived components in a controlled, cGMP cleanroom environment in accordance with Standard Operating Procedures (SOPs) and regulatory requirements. This role operates within a collaborative, shift-based team structure and plays a critical part in ensuring the quality, safety, and timely delivery of life-changing therapies.Shift Schedule: Quad 1 — Sunday through Wednesday, 5:00 AM – 5:30 PM Start and end times are subject to change based on business needs.This position reports directly to the Manufacturing Manager, with day-to-day supervision provided by the shift Supervisor or designated Team Lead.Key ResponsibilitiesProduction & OperationsSet up and operate equipment to support blood component production through cell culture, harvest, and cryopreservationApply aseptic technique for all applicable activities, including tube welding, connections, and transfers; aseptic qualification is requiredWeigh and measure in-process materials to ensure accurate quantities are added or removedAdhere to the production schedule to support on-time, internal production logisticsQuality & ComplianceRecord production data clearly and concisely in accordance with Good Documentation Practices (GDPs)Support deviation investigations and write-ups as neededEnsure on-time closure of assigned CAPAs within the designated shiftPerform all tasks in alignment with site safety policies, quality systems, and GMP requirementsTeam & DevelopmentWork in a team-based, cross-functional environment to fulfill shift production requirementsDevelop subject matter expertise (SME) and become a qualified trainer within a designated manufacturing functionMaintain timely completion of all training assignments to uphold technical skills and process knowledgeContribute to continuous improvement projects, inspection readiness, and right-first-time initiatives, as assignedKnowledge, Skills & AbilitiesBasic understanding of cell culture, cryopreservation, purification, and aseptic processing or laboratory techniqueFamiliarity with cGMP and FDA-regulated industry standardsStrong technical writing capabilityBasic mathematical skills with a general understanding of cGMPsProficiency in Microsoft Office applicationsBackground in biology, chemistry, or medical/clinical practices preferredPrior experience in manufacturing and/or a scientific or engineering disciplineEducation RequirementsWe welcome candidates from a variety of educational backgrounds:Education LevelExperience RequiredBachelor's Degree—Associate's / Medical Technical Degree3+ years in Manufacturing OperationsHigh School Diploma / GED2+ years in Manufacturing or OperationsWorking ConditionsThis role involves working in a specialized cleanroom and laboratory environment. Candidates should be comfortable with the following:Physical Requirements: Intermittent walking and...