Associate I-II, QC Analytics (Contract, Multiple Positions)

ElevateBio
United States
Workplace: OnsiteContractUSD 33 - 48 hourlyFunction: Data Analytics & Business IntelligenceExperience: 1-5 yearsSkills: ["Organizational skills","Attention to detail","Independent work","Communication","Collaboration"]

Support GMP testing in QC laboratories at the BaseCamp facility in Waltham. Perform routine cell and molecular biology assays, analyze and record results, and help with peer review of data and testing reports. Assist with investigating excursions (deviations, CAPAs, OOSs), manage inventory and daily lab operations, and collaborate with Analytical Development and other QC teams to qualify developed assays. Draft and/or edit testing and equipment procedures as needed.

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ElevateBio
ElevateBio
1 day ago

Associate I-II, QC Analytics (Contract, Multiple Positions)

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Last checked: 10 hours agoStatus: Live

Job Summary

Support GMP testing in QC laboratories at the BaseCamp facility in Waltham. Perform routine cell and molecular biology assays, analyze and record results, and help with peer review of data and testing reports. Assist with investigating excursions (deviations, CAPAs, OOSs), manage inventory and daily lab operations, and collaborate with Analytical Development and other QC teams to qualify developed assays. Draft and/or edit testing and equipment procedures as needed.
Location: United States
Workplace: Onsite
Employment Type: Contract · 9 months
Job Function: Data Analytics & Business Intelligence
Seniority: Mid level

Key Responsibilities

  • •Perform routine GMP testing using established test methods, analyzing results and recording/reporting data.
  • •Perform peer-review of data records and testing reports.
  • •Assist with investigating and reviewing testing excursions, including deviations, CAPAs and OOSs.
  • •Collaborate with other QC functions to complete testing within established timelines.
  • •Share responsibility with peers for inventory/reagents management and daily lab operations, and assist with assay qualification and procedure drafting/editing.

Pay and Benefits

Salary: USD 33 - 48 hourly

Key Requirements

  • •Bachelor’s or Master’s degree in a technical discipline (Biology/Molecular Biology/Biochemistry/Chemistry or related field).
  • •1-5 years of experience with a Bachelor’s, or 1-3 years with a Master’s.
  • •Experience working in a GMP setting is preferred.
  • •Experience with cell and gene therapy test methodologies (PCR, Flow Cytometry, ELISA, cell culture, cell-based assays).
  • •Knowledge of GMP, SOPs, and Quality System processes, with experience performing laboratory investigations.
Experience:1-5 yearsCell and gene therapyGMP
Education:
Skills:Organizational skillsAttention to detailIndependent workCommunicationCollaboration
Languages:English
Tech Stack:GMPSOPsQuality SystemPCRFlow CytometryELISACell cultureCell-based assaysLIMSCMMSQMSERP

Company Brief

ElevateBio
Develops and manufactures cell and gene therapies and provides integrated biologics development and manufacturing platforms, partnering with biotech companies to accelerate clinical and commercial production of advanced therapies.
Industry: Biotech
Company Size: Large (251 to 1,000 employees)
Growth: Established Company
Headquarters: Cambridge, United States
Founded: 2017
WebsiteLinkedIn