QC Analytical Associate III
: Job Details :


QC Analytical Associate III

Joule

Location: Mahwah,NJ, USA

Date: 2025-01-08T16:03:28Z

Job Description:
Title: QC Analytical Associate IIILocation: Mahwah, NJ areaSchedule: Sunday to Thursday ( 6:00 am to 2:30 pm)Type: Contract to HireResponsibilities:The Quality Control Analytical Associate III serves as a support role to clinical and commercial production. The QC Analytical Associate III will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility.Under the direction of the Manager, QC Analytical, responsibilities of the QC Analytical Associate III will include but are not limited to: Performs accurate execution of all company and/or client test methods and procedures of cellular products to ensure the safety and/or efficacy of different cell populationsPerforms maintenance, monitoring, and troubleshooting of pertinent equipmentPerforms and assists in the training of other Quality Control Analytical AssociatesMaintains training records and coordinates records retention with Document Control and Training groupsTests, documents, and reports results for products or materials following company and/or client procedures following CGMP and/or GTP guidelinesPerforms state proficiency testing and/or client proficiency testing under direct supervision as applicableParticipates in managing QC materials and suppliesPerforms and assists in equipment and method qualification/validation activities as neededPerforms reagent and media preparationProvides input based on level of knowledge and experience with troubleshooting malfunctioning equipmentLeads investigations for out-of-specification, out-of-trend, aberrant, and/or non-conforming test resultsDetermines root causes and implements intelligent corrective and preventive actions (CAPAs) and monitors CAPA effectivenessInitiates, investigates, and prepares deviation reports with input from assigned supervisorBrainstorms and implements corrective and preventive actions, as and when applicableDocuments training and execution of shipping test samples to contract laboratories for testingCompletes all documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP)Ensures timely issuance, review, and approval of Certificate of Analysis, alongside timely closures of batch records, deviations, and CAPAInitiates, assesses, approves, tracks, and trends deviations, Change Controls and CAPAsCommunicates effectively with other co-workers, departments, management and clientsEventually serves as a lead and/or co-lead for client projectsManages and drives resolution of quality issues with clients, collaborators, and internal personnelMakes informed and independent decisions on complex issues in collaboration with key stakeholders and alignment with company policies.Manages completion of document changes and maintains the internal QC change control systemApplies expertise of compliance requirements and therefore maintains an inspection-ready state laboratoryParticipates as subject matter expert during audits/inspectionsWorks with internal departments and outside vendors, collaborators, and partners effectively for meeting projects timelines and commitmentsAdditional tasks as assignedRequirements: BA/BS in a science or relevant field requiredMS is preferredPrior cGMP experience requiredPrior QC laboratory, clinical laboratory, microbiology, hematology, blood banking, or immunology experience in a CGMP/GTP environment a mustGMP, Cell count, flow cytometry , documentation, flexibility, CBC, Endotoxin, ELISA, qPCR, Quality records (DRs, CAPA, CC, Docs revision) Fluency, multitasking, agilityPrior industrial experience in cell count methodologies preferredPrior academic and/or industrial cell therapeutic experience preferredMinimum 4-6 years of experience in Quality Control laboratory setting or within the biopharmaceutical industryProficient with computer software such asMicrosoft OfficeVisioBenefitsSystem One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.
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