• Perform mouse in vivo animal procedures, including tumor inoculation and dosing mice.
• Responsible for monitoring all in-life study measurements.
• Measure tumors by calipers and non-invasive imaging, body weight, and tracking.
• Overall health condition and survival of mice.
• Share responsibilities in maintaining lab equipment and reagent inventory
• Perform cell cultures to enable inoculation of tumor cells and primary cells
• Follow laboratory safety guidelines and practices.
• Design and execute experimental plans that support project progression
• Leading to the publication of novel biology ideally.
• Present experiments and results at project team meetings, group meetings, and company meetings.

Skills: In Vivo Animal Procedures, Health Monitoring, Measurement Techniques, Laboratory Maintenance, Cell Culture Techniques, Safety Compliance, Experimental Design and Execution, Presentation and Communication Skills

• Developing and executing cell-based and biochemical assays.
• Evaluate the potency and mechanism of action of novel compound indications.
• Generate, analyze, and evaluate high-quality data critical to moving projects forward.
• Advance group capabilities and know-how by identifying and implementing novel technologies.
• Collaborate within and across teams, including mentoring others on areas of expertise.
• Activate and expand primary T cells for functional tests.
• Transduce primary T cells and target cell lines using lentivirus.
• Quantify surface levels of chimeric antigen receptors using immunofluorescence staining.
• Perform assays for T cell activation, tumor cell killing, and cytokine release.
• Responsible for experimental design and data analysis using Prism and Excel.

Skills: Cell-Based Assay Development and Execution, Biochemical Assay Proficiency, Data Analysis and Interpretation, Technological Innovation, Collaborative Teamwork, Primary T Cell Manipulation, Lentiviral Transduction, Immunofluorescence Staining and Quantification

• Support the molecular cloning of chimeric antigen receptor constructs.
• Maintaining cell lines for in vitro studies.
• Designing, executing, and reporting biotransformation studies.
• Supporting drug discovery/development and regulatory filings. 
• Develop LC-MS methods for separation, structural identification of multiple metabolites.
• Designing and implementing appropriate assays and strategies.
• Support the development of small molecules, peptides, and other novel modalities. 
• Evaluate new technologies, and establish DMPK screening criteria for discovery projects.
• Maintain accurate records and write in vitro ADME reports for in-house studies.
• Presenting data/strategy to scientists and management internally.

Skills: Molecular Cloning, Cell Line Maintenance, Biotransformation Studies, Drug Discovery and Development, LC-MS Method Development, Assay Design and Implementation, Support for Novel Modalities, DMPK Screening Criteria, Record Keeping and Reporting, Presentation Skills

• Perform state-of-the-art multi-color flow cytometry methods for the characterization of cell therapy manufacturing processes and products.
• Provide analytical support, including qualification of in-process and release methods and tech transfer internally and externally.
• Contribute to project technical teams to ensure effective communication at all levels. 
• Collaborate effectively to ensure productive interactions with all stakeholder groups.
• Ensure high-quality, timely documentation in electronic laboratory notebooks and technical reports.
• Configure and be the principal administrator of a laboratory information system providing applications.
• Responsible for media preparation, thawing and seeding, feeding, passaging, and cryopreservation of cells.
• Assist in the operation of bioreactors for scale-up of mammalian cell culture.
• Assist in planning and implementing the development of new processing materials, procedures, and products.
• Assist in establishing process parameters and improving manufacturing efficiencies.

Skills: Multi-color flow cytometry expertise, Analytical skills, Communication skills, Collaboration, Documentation, Laboratory information system (LIS) administration, Cell culture techniques, Bioreactor operation

• Managing the backend database and web server.
• Providing support and solutions for end-user requests and issues.
• Perform analysis and create visualizations from high throughput sequencing, large datasets.
• Responsible for data mining of public and internal datasets.
• Responsible for extraction and storage into relational or graph databases.
• Responsible for the application of academic and internal toolkits and pipelines.
• Utilize statistical analysis and machine learning algorithms.
• Responsible for uncovering new insights within informatics deliverables.
• Work with other Process Science and Technology team members.
• Maintain accurate records and assist scientists with recording experimental data.

Skills: Database Management, End-user Support, Data Analysis and Visualization, Data Mining, Toolkit Utilization, Statistical Analysis and Machine Learning, Informatics Insights, Collaborative Work, Record Maintenance

• Perform short and long-term cell culture experiments.
• Maintain adherent and suspended mammalian cell cultures.
• Work with the in-house team to develop and optimize processes for cell-based screening.
• Contribute to the implementation of molecular, cellular, and viral biology workflows in the laboratory
• Responsible for optimization of cloning, cell line transduction/transfection, qPCR/ddPCR, NGS-based analysis.
• Support the small-scale manufacturing of viral vectors and associated analytics.
• Support the establishment of a new laboratory.
• Ensuring accurate record-keeping and experimental write-up.
• Keeping in-house electronic records (inventories, stock systems) up-to-date.
• Complete projects and prepare reports within agreed timelines.

Skills: Cell Culture Techniques, Process Development, Molecular and Cellular Biology, Analytical Skills, Viral Vector Manufacturing, Laboratory Establishment, Record-Keeping, Project Management

• Perform both routine and non-routine assignments, utilize various types of instrumentation and matrices.
• Participate in regulatory compliance activities and technical interactions with clients.
• Ensure the testing of client samples and reporting of results is accomplished in a timely and accurate manner.
• Prepare and implement deviations, laboratory investigations, and CAPAs.
• Perform equipment maintenance and troubleshooting.
• Investigate and facilitate the solving of any equipment failures.
• Participate in various tasks including method design, development, validation, and analysis.
• Perform custom protocols and validations within the operational area
• Responsible for writing final reports to support these activities.
• Determine opportunities to increase efficiency and implement process improvements.

Skills: Routine and Non-routine Assignments, Instrumentation Expertise, Regulatory Compliance, Timely and Accurate Testing, Deviations, Investigations, and CAPAs, Equipment Maintenance and Troubleshooting, Method Development and Validation, Custom Protocols and Validations

• Develop, optimize, validate, and perform biological cell-based assays
• Assist in experimental design with the support of the project leader.
• Assess the effects of putative therapeutics and analyze the associated data.
• Establish an understanding of the relevance of the data being generated on the project.
• Write up lab book to the department and patent-acceptable standard.
• Highlight interesting biology papers for the project team.
• Use appropriate scientific literature to plan assays.
• Maintain a strong awareness of the relevant scientific literature, and contemporary laboratory practices.
• Perform work in a BSL-2 laboratory including processing clinical specimens, and bacterial culture propagation.
• Responsible for maintenance, and susceptibility testing.

Skills: Assay Development and Optimization, Experimental Design, Data Analysis and Interpretation, Scientific Documentation, Literature Review and Application, Laboratory Safety and Protocol Compliance, Technical Laboratory Skills, Communication and Team Collaboration

• Develop and write protocols and SOPs with assistance.
• Train to Study Direct efficacy and safety pharmacology studies
• Conceive and conduct experimentation with guidance from senior team members from project inception.
• Analyze data, form conclusions, and determine future experimental plans.
• Recommend expansion or curtailment of activities based on the latest information.
• Assume responsibility for the timely completion of projects, consistent with the project's critical path.
• Work under the supervision of scientists and engineers to conduct research.
• Responsible for study plan generation, in-life execution, data analysis, and reporting
• Identifying appropriate animal models for commercial development to support respiratory efficacy studies
• Maintaining high-quality, accurate records under the regulatory standards of Good Laboratory Practice.

Skills: Protocol and SOP Development, Study Directing and Training, Experimentation, Data Analysis and Interpretation, Decision Making, Project Management, Research Collaboration, Study Plan Generation and Execution, Animal Model Selection, Record-Keeping and Compliance.

• Perform a wide range of pharmacological in vivo techniques.
• Perform pre-clinical studies according to the study plans, and Standard Operating Procedure.
• Assist in the design/customization of study plans for the development of animal models.
• Responsible for preparing accurate, high-quality scientific reports.
• Analyze and report experimental data to Sponsors and internal stakeholders.
• Responsible for biochemical and cell-based assays, HPLC separation, and data analysis.
• Perform existing analytical procedures, and ensure analytical results are of high quality.
• Ensure all work is documented in a clear, concise, and timely manner.
• Communicate results to customers in a timely fashion to enable team decisions.
• Perform assay qualification and robustness experiments.

Skills: In Vivo Pharmacological Techniques, Pre-clinical Study Execution, Study Plan Design and Customization, Scientific Report Preparation, Data Analysis and Reporting, Biochemical and Cell-based Assays, Analytical Procedure Execution, Documentation and Communication

• Experience working in veterinary medicine/laboratory animal or related field.
• Ability to learn new technology and apply it appropriately with minimal supervision
• Good communication and interpersonal skills.
• Experience in a diagnostic laboratory, CNAS and/ or CMA, or PCR and serology testing.
• Proven experience in safe handling of potentially hazardous biological materials and equipment.
• Experience working in disease, disease pathogens, and/or animal health.
• Problem-solving and troubleshooting abilities.
• Ability to work in a collaborative work environment with a team.
• Experience in routine bench work and/or instrumental analysis.
• Proficiency in executing standard procedures required in addition to non-routine work.

Qualifications: BA in Neuroscience with 5 years of Experience

• Must be familiar with basic scientific principles.
• Knowledge of Chemical Engineering, Biochemical Engineering, or Life Sciences.
• Ability to identify, develop, and implement solutions to practical problems.
• Basic understanding of protein chromatography, filtration, or cell culture principles.
• Hands-on experience with mammalian cell culture, and/or purification operations.
• Prior experience with data analytical tools (Excel, Spotfire, etc.). 
• Experience with statistical analysis and programming in JMP, R, and/or Python environments.
• Motivated self-starter with excellent interpersonal and organizational skills.
• Team player with the ability to work within a diverse team in a dynamic, cross-functional environment.
• Familiar with the design of experiments and statistical analysis of data.

Qualifications: BS in Pharmacology with 6 years of Experience

• Knowledge of applicable regulatory authority, compendia, and ICH guidelines.
• Experience in pharmaceutical research and development or in providing analytical chemistry support.
• Working knowledge of modern biological analytical techniques
• Experience in HPLC, immunological assays (ELISA), gel and capillary electrophoresis, qPCR, etc.
• Understanding of chromatographic methods, use of analytical tools, and other pharmaceutical analysis.
• Ability to work effectively in team situations and to work independently. 
• The flexibility to succeed in a dynamic and changing environment.
• Excellent verbal, written, and interpersonal communication skills.
• Ability to utilize Microsoft Excel and Word to perform tasks.
• Good written and oral communication skills.

Qualifications: BA in Molecular Biology with 4 years of Experience

• Fundamental knowledge of cGMP compliance requirements and pharmaceutical stability principles.
• Previous working experience in the pharmaceutical industry.
• Good documentation skills with general computer skills (MS Excel, Word, Internet Explorer, PowerPoint).
• Ability to author and review standards, guidelines, SOPs, templates, protocols, and other GMP documentation.
• Ability to compile, summarize, and present information to diverse groups.
• Excellent communication skills with a customer-focused attitude.
• Be willing to interact with laboratory personnel, contractors, and management.
• Ability to troubleshoot problems and identify solutions.
• Time management and project management skills.
• Ability to partner with individuals outside of a formal reporting relationship toward the realization of team goals.

Qualifications: BS in Biotechnology with 6 years of Experience

• Good knowledge of standard molecular biology/nucleic acid-based protocols for both DNA and RNA.
• Experience in oncology and/or IVD product development.
• Solid understanding of scientific principles with strong laboratory skills.
• Ability to work independently and in a team setting.
• Be detail-oriented and well-organized.
• Able to implement protocols and keep good notes in a lab notebook.
• Knowledge of standard molecular biology/nucleic acid-based protocols for DNA.
• Ability to handle hazardous and biohazardous materials including human blood products.
• Excellent communication skills, both written and verbal.
• A desire to be part of fast fast-paced dynamic development environment.

Qualifications: BA in Microbiology with 4 years of Experience

• Excellent knowledge of cGMP guidelines and standards.
• Must be capable of following written instructions with the ability to troubleshoot.
• Have clear written communication skills and computer literacy.
• Knowledge of Chemistry, Material Science, Biomedical Engineering, or Biochemistry.
• Prior experience working in a scientific laboratory and using benchtop/analytical instrumentation.
• Must be comfortable working with biological materials.
• Good documentation skills with general computer skills.
• Ability to work with a cross-functional team in a matrix environment.
• Curiosity about new digital approaches and innovative technologies.
• Flexible, pragmatic, and goal-oriented working style and scientific way of thinking.

Qualifications: BS in Genetics with 3 years of Experience

• Experience working in a laboratory setting.
• Prior experience working with general microbiology techniques.
• Knowledge of the following industry regulations FDA (Food and Drug Administration), GMP (Good Manufacturing Practice), QSR (Quality System Regulation), ISO (International Organization of Standardization).
• Knowledge of PC spreadsheet, word processing, and database applications.
• Excellent verbal and written communication skills.
• Work independently and as a member of a team.
• Good practical knowledge of laboratory and/or technical equipment.
• Team spirit and an agile mind.
• Good communication and interpersonal skills.

Qualifications: BA in Immunology with 5 years of Experience

• Basic laboratory skills, including analytical weighing, sample preparation and dilution, treatment application, insect culture maintenance, test evaluations.
• Ability to work safely in a fast-paced team environment.
• Be willing to work with chemicals of unknown toxicological hazard under strict safety measures.
• Familiar with conducting greenhouse, controlled environment chamber, and laboratory bioassays.
• Must have strong critical thinking capabilities.
• Excellent written and oral communication skills.
• Good computer skills with an ability to learn new proprietary software.
• Ability to work in a team environment to achieve group objectives.
• Ability to share technical knowledge with others and promote the development of the team.
• Strong organizational skills with learning agility.

Qualifications: BS in Cell Biology with 3 years of Experience

• Knowledge of lab safety, relevant applications, raw materials, and chemical processes.
• Working experience in Science and Technology, or Chemistry.
• Able to have creativity and novel approaches to solving scientific problems.
• Intellectually curious and well-informed on the latest scientific advances in the field.
• Detail-oriented, with excellent record-keeping skills.
• Must have Certification of Regularization by the Federation of European Laboratory Animal Science Associations (FELASA), or similar foreign certification.
• Excellent oral and written communication skills. 
• Able to effectively present scientific data and concepts to international standards.
• Excellent interpersonal skills with the ability to interact effectively with people, internally and externally.
• Be part of a motivated and experienced research team in an innovative working environment.

Qualifications: BA in Pharmaceutical Sciences with 4 years of Experience

• Experience in fragrance/flavor or fast-moving consumer goods industry.
• Ability to operate and troubleshoot GC/MS.
• Strong interpretation ability on GC/MS data.
• Knowledge of analytical chemistry and related fields, regulatory standards, and procedures.
• Must have Functional or Technical Skills.
• Be part of creative project teams and be a team player.
• Ability to the activity and inhibition kinetics analysis, ELISA, Protein quantitation, Western blot.
• Practical knowledge of SDS-PAGE, spectroscopy, and thermodynamics of folding/unfolding.
• Strong organizational and communication skills (written and verbal).
• A detailed scientific approach, and multi-task.

Qualifications: BS in Bioinformatics with 6 years of Experience