MaxCyte, IncNewField Applications Scientist MaxCyte, IncField Applications ScientistRaleigh, NCThe Field Applications Scientist (FAS) provides technical and troubleshooting support to customers of MaxCyte’s Scalable Transfection Systems, with primary focus on cell therapy and protein production/expression but will work with customers in multiple application areas. You will also play a key role in pre-sales, helping identify high-potential projects and educating customers on off-target risk assessments for cell & gene therapy, highlighting our SeQure Services portfolio.
Encoded TherapeuticsNewAnalytical Sciences Associate Encoded TherapeuticsAnalytical Sciences AssociateMorrisville, NCPerform routine analytical testing to support GMP release, stability, and product characterization programs, including cell-based potency assays, molecular assays (e.g., ddPCR), and/or biochemical assays (e.g., ELISA, CE, HPLC, Western blot), with primary depth in at least one assay category. Hands-on experience in at least one of the following areas required, with working knowledge or exposure to others preferred: Cell-based potency assays, Molecular assays, or Biochemical assays (ELISA, CE, HPLC, Western blot).
Beam TherapeuticsManufacturing Sciences & Technology (MS&T) Co-op Beam TherapeuticsManufacturing Sciences & Technology (MS&T) Co-opDurham, NC$23–$34 / hourBeam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. Under the guidance of their mentor, the MS&T co-op will support the following: Develop a project plan, define objectives and desired outcomes, engage and collaborate with cross-functional partners and stakeholders, and meet timelines.
Beam TherapeuticsQC Analytical Methods Co-op Beam TherapeuticsQC Analytical Methods Co-opDurham, NC$23–$34 / hourThe co-op will support lab readiness by gaining understanding of analytical methods, coordinating equipment onboarding activities, assisting with qualification and validation documentation, supporting build-out efforts, maintaining laboratory materials, and gaining practical experience with GxP workflows and equipment processes. The role offers hands-on exposure to Quality Control operations in a regulated environment, including equipment onboarding and validation, cross-functional collaboration with external equipment vendors and internal teams such as QC, Facilities, Validation and Project Management teams.
Leadstack IncQuality Control Analyst I Leadstack IncQuality Control Analyst IResearch Triangle Park, NC$28–$30 / hourPreferred Education, Experience and Skills Relevant work experience (0-2 years) in areas such as, analytical testing, development, and technology transfer; in rAAV/gene therapy, recombinant protein/biomolecules, and/or. The purpose of the Analyst I, Quality Control (Non-Clinical) is to perform analytical testing to support the release of Non-Clinical grade rAAV vector lots manufactured in various .
Alcami CorporationSr. Scientist II - Biotech , Mass Spec Alcami CorporationSr. Scientist II - Biotech , Mass SpecDurham, North CarolinaA Senior Scientist II in this role routinely executes method development/method validation projects, troubleshoots equipment, documents proficiently in electronic laboratory notebooks, prepares and reviews summaries of observations, test procedures and project reports, and is capable of verbal and written presentations to internal and external audiences. Demonstrated experience in development, validation and troubleshooting chromatographic, electrophoretic, mass spectrometry and other spectroscopic methods for one or more of the following products: peptides, monoclonal antibodies/recombinant proteins, nucleic acids, cell therapy, and gene therapy.
LanceSoft IncQuality Control Analyst LanceSoft IncQuality Control AnalystDurham, NCFull timeThe purpose of the Analyst I, Quality Control (Non-Clinical) is to perform analytical testing to support the release of Non-Clinical grade rAAV vector lots manufactured in various departments (including, Pre-Clinical Manufacturing, Process Development, MSAT) and external partners. Preferred Education, Experience and Skills: Relevant work experience (0-2 years) in areas such as, analytical testing, development, and technology transfer; in rAAV/gene therapy, recombinant protein/biomolecules, and/or other advanced therapeutic modalities.
IntelliPro Group Inc.Lab Quality Control IntelliPro Group Inc.Lab Quality ControlResearch Triangle Park, NCThe purpose of the Analyst I, Quality Control (Non-Clinical) is to perform analytical testing to support the release of non-clinical grade rAAV vector lots manufactured in various departments (including, Pre-Clinical Manufacturing, Process Development, MSAT) and external partners. Preferred Education, Experience and Skills:Relevant work experience (0-2 years) in areas such as, analytical testing, development, and technology transfer; in rAAV/gene therapy, recombinant protein/biomolecules, and/or other advanced therapeutic modalities.