Specialist, QC analytical

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 JobsSpecialist, QC analyticalSummit West - NJ - US No longer accepting applications.Job IDR1603714Date posted06/21/2026DepartmentCell TherapyPosition SummaryResponsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. May assist with method transfer, documentation, deviations, investigations, and continuous improvement efforts.Hours are Wednesday to Saturday, 1:30 PM to 11:30 PM ET.Role is fully onsite.Duties/ResponsibilitiesPerform routine testing of in-process, final product, and stability samples.Perform testing for method transfer/validation/verification.Perform data verification, data review and review of GMP documentation for general methods.May perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.Train analysts on general job duties.Perform other tasks as assigned.Reporting RelationshipThis position will report to QC management.QualificationsSpecific Knowledge, Skills, Abilities:Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.Knowledge of LIMS, ELN and laboratory data analysis systems preferred.Problem-solving ability/mentality, technically adept and logical.Ability to communicate effectively with peers, department management and cross-functional peers.Experience with writing technical documents preferred.Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.Education/Experience/ Licenses/Certifications:Bachelor's degree or equivalent required, preferably in science.  Netherlands: Bachelor's degree / HLO in (bioanalytical) science preferred. MLO level 4 with equivalent combination of work experience may be considered.2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.Demonstrated experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, ELISA, and aseptic technique).Position SummaryResponsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. May assist with method transfer, documentation, deviations, investigations, and continuous improvement efforts.Hours are Wednesday to Saturday, 1:30 PM to 11:30 PM ET.Role is fully onsite.Duties/ResponsibilitiesPerform routine testing of in-process, final product, and stability samples.Perform testing for method transfer/validation/verification.Perform data verification, data review and review of GMP documentation for general methods.May perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.Train analysts on general job duties.Perform other tasks as assigned.Reporting RelationshipThis position will report to QC management.QualificationsSpecific Knowledge, Skills, Abilities:Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.Knowledge of LIMS, ELN and laboratory data analysis systems preferred.Problem-solving...