QC Analytical Associate

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 JobsQC Analytical AssociateLeiden – NL No longer accepting applications.Job IDR1604341Date posted07/09/2026DepartmentCell TherapyPosition summaryResponsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts.Responsibilities• Perform routine testing of in-process, final product, and stabilitysamples.• May review GMP documentation and perform data verification.• Support document revision, project, CAPA and deviation/ investigationrelated tasks and/ or continuous improvement efforts.• May train analysts on general job duties.• Perform other tasks as assigned.QualificationsSpecific Knowledge, Skills, Abilities:• Ability to accurately and completely understand and followprocedures.• Apply scientific principles to analytical testing and the proper use oflaboratory equipment.• Ability to communicate effectively with peers and managementregarding task completion, roadblocks, and needs.• Attention to detail and demonstrated organizational skills.• Ability to work in a fast-paced team environment, meet deadlines, andprioritize work.Education/Experience/ Licenses/Certifications:• Bachelor's degree preferred in science. Associate’s degree withequivalent combination of education and work experience may beconsidered. Netherlands: Bachelor's degree /HLO in (bioanalytical)science preferred. MLO level 4 with equivalent combination of workexperience may be considered.• 0-2+ years of relevant analytical testing or QC experience orequivalent combination of education and experience, preferably in aregulated environment.• Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.• Prior experience in cell and molecular biology techniques (e.g., cell based assays, flow cytometry, qPCR, aseptic technique) is preferred.#LI-HybridPosition summaryResponsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts.Responsibilities• Perform routine testing of in-process, final product, and stabilitysamples.• May review GMP documentation and perform data verification.• Support document revision, project, CAPA and deviation/ investigationrelated tasks and/ or continuous improvement efforts.• May train analysts on general job duties.• Perform other tasks as assigned.QualificationsSpecific Knowledge, Skills, Abilities:• Ability to accurately and completely understand and followprocedures.• Apply scientific principles to analytical testing and the proper use oflaboratory equipment.• Ability to communicate effectively with peers and managementregarding task completion, roadblocks, and needs.• Attention to detail and demonstrated organizational skills.• Ability to work in a fast-paced team environment, meet deadlines, andprioritize work.Education/Experience/ Licenses/Certifications:• Bachelor's degree preferred in science. Associate’s degree withequivalent combination of education and work experience may beconsidered. Netherlands: Bachelor's degree /HLO in (bioanalytical)science preferred. MLO...