• Sr. Scientist, Cell Therapy R&D (Telford, PA)
    on July 29, 2021 at 6:46 pm

    Sr. Scientist, Cell Therapy R&D (Telford, PA)SNAPSHOT!Our client engineers biomaterials to facilitate the repair, recovery, and regeneration of the human body. Throughout the pproduct lifecycle, they provide clients with consistent value, quality, and technical expertise. Our mission is to continually advance biomaterials technology into practical applications for the medical device and pharmaceutical industries.Their business partnerships focus on quality, responsiveness, communication, and continuous improvement throughout the product lifecycle and beyond.To achieve this mission, they are dedicated to certain values, innovation, communication, quality, responsiveness, and continuous improvement. Immediate need for a Sr. Scientist, Cell Therapy R&D in Telford, PA who possess:MS degree in the field of Biological Sciences, Cell Biology, Bioengineering, Chemistry, Biology, Biomedical Engineering, Materials Science or equivalent. PhD is highly desirable.3+ years’ direct experience in cell therapy manufacturing.Ability to work in a high paced team environment, meet deadlines, and prioritize work on multiple projects.Knowledge of autologous and allogenic CAR T processing.Practical experience with mammalian cell culture, fluorescence imaging, cell health and viability assays, flow cytometry, PCR. Experience with T Cell or Pluripotent SC culture is highly desirable.Prior work experience in a regulated environment (ISO 9001, 13485 and QSR Standards) a plus.Ability to accurately analyze data generated by various analytical and physical testing instrumentation.Solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.Key responsibilities include:Working both independently and within a small multidisciplinary team, drive the development of novel solutions for cell processing and expansion in CAR T and other cell manufacturing platforms.Serve as cell biology subject matter expert and provide technical leadership to others and make decisions to set directions for multiple projects.Develop and perform analytical assays to characterize manufacturing process steps.Collaborate with business development to understand unmet needs and customer requirements for cell processing.Define, participate in, and manage CMO and CDMO relationships.Reviews and critically assesses patents and other forms of intellectual property.Actively develops intellectual property through the filing of patent applications.Clearly communicates technical information and project status to supervisor and colleagues through written and verbal means.Accurately and thoroughly documents procedures and results using laboratory notebooks, protocols & reports, records and databases.Effectively collaborates with colleagues on laboratory techniques, sample preparation, instrumentation, data analysis and documentation.Follows all applicable Company test methods, work instructions, S.O.P.’s, and guidelines.Performs other job-related responsibilities as assigned .For immediate considerations please email your resume to admin@snapstaffing.com

  • Sr. Scientist, Bioconjugation (Telford, PA)
    on July 29, 2021 at 6:45 pm

    Sr. Scientist, Bioconjugation(Telford, PA)SNAPSHOT!Our client engineers biomaterials to facilitate the repair, recovery, and regeneration of the human body. Throughout the pproduct lifecycle, they provide clients with consistent value, quality, and technical expertise. Our mission is to continually advance biomaterials technology into practical applications for the medical device and pharmaceutical industries.Their business partnerships focus on quality, responsiveness, communication, and continuous improvement throughout the product lifecycle and beyond.To achieve this mission, they are dedicated to certain values, innovation, communication, quality, responsiveness, and continuous improvement.  Immediate need for a Sr. Scientist, Bioconjugation in Telford, PA, who possess:PhD degree in the field of Polymer Science, Bioengineering, Chemistry, Biology, Immunology, Materials Science or equivalent.3+ years’ relevant industrial experienceHands-on Experience with antibody/drug conjugation techniques, particle chemistry and surface scienceExperience with liposome/lipid nanoparticle formation, development, and characterization strongly desiredDemonstrated proficiency with materials and particle characterization using modern chromatography methods, NMR, thermal analysis, mass spectrometry, rheology, light scattering, fluorescence imaging, spectroscopic analysis, Zeta potentialKnowledge of autologous and allogenic CAR T processingAbility to work in a high paced team environment, meet deadlines, and prioritize work on multiple projects.Ability to accurately analyze data generated by various analytical and physical testing instrumentationSolve practical problems and deal with a variety of concrete variables in situations where only limited standardization existsKey responsibilities include:Working both independently and within a small multidisciplinary team, drive the development of novel biomaterial solutions for CAR T manufacturing and therapeutic deliveryDesign and perform antibody/drug conjugation and characterization on a variety of polymeric substrates with varying morphologiesDevelop nano/microparticle products utilizing a portfolio of synthesis techniques, including polymerization, precipitation, chemical conjugation, emulsions, liposomes, micelles.Characterize particles and surfaces using microscopy, spectroscopy, surface energy, Zeta potential and particle size analysisExperience with polymer chemistry principles and antibody and protein conjugationsCollaborate with business development to understand unmet needs and customer requirementsDefine, participate in, and manage internal and external collaborationsReviews and critically assesses patents and other forms of intellectual propertyActively develops intellectual property through the filing of patent applicationsClearly communicates technical information and project status to supervisor and colleagues through written and verbal meansAccurately and thoroughly documents procedures and results using laboratory notebooks, protocols & reports, records and databasesEffectively collaborates with colleagues on laboratory techniques, sample preparation, instrumentation, data analysis and documentationFollows all applicable Company test methods, work instructions, S.O.P.’s, and guidelinesPerforms other job-related responsibilities as assignedFor immediate considerations please email your resume to admin@snapstaffing.com

  • Nanoparticle Sr. Scientist (Telford, PA)
    on July 29, 2021 at 6:45 pm

    Nanoparticle Sr. Scientist (Telford, PA)SNAPSHOT!Our client engineers biomaterials to facilitate the repair, recovery, and regeneration of the human body. Throughout the pproduct lifecycle, they provide clients with consistent value, quality, and technical expertise. Our mission is to continually advance biomaterials technology into practical applications for the medical device and pharmaceutical industries.Their business partnerships focus on quality, responsiveness, communication, and continuous improvement throughout the product lifecycle and beyond.To achieve this mission, they are dedicated to certain values, innovation, communication, quality, responsiveness, and continuous improvement.  Nanoparticle Sr. Scientist in Telford, PA, who possess:PhD degree in the field of Polymer Science, Bioengineering, Chemistry, Materials Science, Biomedical Engineering, or equivalent.3+ years’ relevant industrial experience.Extensive hands-on experience developing liposome/lipid nanoparticle systems for targeted delivery applications to cellsExperience generating nanoparticles containing nucleic acids for delivery to cells.Experience with microfluidics, emulsions, polyplexes, encapsulation technologies strongly desired.Demonstrated proficiency with materials and particle characterization using modern chromatography methods, light scattering, fluorescence imaging, spectroscopic analysis, Zeta potential.Ability to work in a high paced team environment, meet deadlines, and prioritize work on multiple projects.Ability to accurately analyze data generated by various analytical and physical testing instrumentation.Key responsibilities include:Working both independently and within a small multidisciplinary team, drive the development of novel nanoparticle-based delivery solutions for cell and gene therapies.Develop nano/microparticle products utilizing a portfolio of synthesis techniques, including polymerization, precipitation, chemical conjugation, emulsions, liposomes, micelles.Characterize particles and surfaces using microscopy, spectroscopy, surface energy, zeta potential and particle size analysis.Familiarity of polymer chemistry principles and antibody and protein conjugations.Collaborate with business development to understand market needs and customer requirements.Define, participate in, and manage internal and external collaborations.Reviews and critically assesses patents and other forms of intellectual property.Actively develops intellectual property through the filing of patent applications.Clearly communicates technical information and project status to supervisor and colleagues through written and verbal means.Accurately and thoroughly documents procedures and results using laboratory notebooks, protocols & reports, records and databases.Effectively collaborates with colleagues on laboratory techniques, sample preparation, instrumentation, data analysis and documentation.Follows all applicable Company test methods, work instructions, S.O.P.’s, and guidelines.Performs other job-related responsibilities as assigned.For immediate considerations please email your resume to admin@snapstaffing.com

  • CLS, Irvine, CA
    on July 20, 2021 at 9:02 pm

    CLS (Irvine, CA)SNAPSHOT!Our client is a clinical toxicology laboratory located in Irvine, California. Their primary focus is providing urine drug test results to addiction treatment providers as well as other medical providers in sectors that necessitate the detection and monitoring of illicit and prescription drugs.Immediate opening for a CLS, Irvine, CA, who possesses:Fully licensed clinical laboratory scientist in CaliforniaAbSciex experience, proficient in MultiquantHigh attention for detailExcellent written and communication skillsDuties and Responsibilities:Perform toxicology testing in a high complexity CLIA laboratory and associated daily quality related testing activitiesContribute to SOP writingAbility to answer client phone callsPerform validation testingMaybe assigned other duties contributing to the overall quality, compliance and operational function of the laboratoryIf you’d like to explore, send your resume to admin@snapstaffing.com and we’ll follow up with you ASAP!

  • Senior Scientist/Principal Scientist, Clinical Biomarker & Bioanalysis (Cambridge, MA)
    on July 20, 2021 at 8:43 pm

    Scientist/Principal Scientist, Clinical Biomarker & Bioanalysis (Cambridge, MA)SNAPSHOT!Looking for a chance to join a team that is pathing the way for cancer immunotherapies as a Scientist/Principal Scientist, Clinical Biomarker & Bioanalysis?? READ ON!!Our client harnesses the immune system to reveal the optimal targets for each patient to develop cancer immunotherapies that will be better, more accessible and more affordable. Their proprietary technology is a clinically validated platform that selects therapeutically relevant antigens that drive powerful anti-tumor immune responses. This technology is the only platform able to identify personal neoantigens that drive suppressive T cell responses, abrogate protection of therapeutic anti-tumor vaccines that can reverse or dampen the immune responses.Immediate opening for a Senior Scientist/Principal Scientist, Clinical Biomarker & Bioanalysis, Cambridge, MA, who possesses:Proficient in multi-color flow cytometry and ligand binding assay design and executionExperienced in fit-for-purpose clinical biomarker assay validation or bioanalytical assay validationSkilled in clinical study sample analysis in a regulated setting compliant with GxP guidelinesExperienced in SOP development/update, study report generation, and critical review of raw data and study resultsExperienced in managing direct reportsExperienced in delivering clinical biomarker and bioanalytical data in the regulated settingSubject matter expert in the development and validation of clinical-grade assays (flow cytometry and/or ligand binding assays)Strong knowledge in GLP/GDP and regulatory guidelines for assay validation and clinical study sample analysisExperience in immuno-oncology and cell therapy product developmentExcellent ability to perform hands on experiments, research, design, and organize projects and maintain detailed documentationDuties and Responsibilities:Support clinical biomarker strategies for cancer cell therapyLead by model, responsible for leading flow cytometry and/or ligand binding assay validation and clinical study sample analysisResponsible for maintaining regulatory compliance appropriate for clinical study data generation and documentation. Subject matter expertise in GLP/GDP guidelinesResponsible for SOP development/update, report generation, QC and review of raw data and resultsLeverage external contract research organizations and vendors along with appropriate internal laboratories to execute biomarker analysisMentor junior scientists in clinical-grade assay development, validation, data generation and analysisParticipate in continuous improvement of scientific and regulatory processes to enhance functional capabilities and productivityEffective communications and collaborations across functional linesIf you’d like to explore, send your resume to admin@snapstaffing.com and we’ll follow up with you ASAP!