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Global Product Development and Supply - Cell Therapy Analytical Development (CTAD) Job Number: 26-00847 Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for a Global Product Development and Supply - Cell Therapy Analytical Development (CTAD) for our client in Summit, NJ. ECLARO’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity! Position Overview: The Analyst is responsible for supporting the method transfer and analytical testing with moderate supervision as part of Cell Therapy Technical Operations (CTTO) Team. The analytical department is responsible for flow cytometry, cell-based potency, RT-qPCR/PCR and other analytical assays testing to support process characterization testing of the lentiviral vector and cell therapy drug product samples. This includes the ability to interface with multiple groups, independently perform tasks, interpret results, and troubleshoot. Responsibilities: 100% onsite required. Perform experiments using the following methodologies: PCR, RT-qPCR, flow cytometry, mammalian cell culture, Luminex, MSD, and ELISA. With moderate supervision design and execute analytical experiments of moderate complexity. Perform data analysis, summarize and report experimental results. Document/review laboratory work in notebooks that is detailed, accurate, timely, and in compliance with Good Lab Practices/Good Documentation Practices requirements. Collaborate with the Quality Control and Analytical Development teams to advance analytical and development projects. Ensure proper operation and perform routine maintenance of all laboratory equipment. Utilize scientific principles to assist in analytical testing methods and the proper use of laboratory equipment. Perform cell based in-vitro flow experiment, ELISA, qPCR to assess critical reagent concentration. Capable of handling complex issues and solving problems with only general guidance. Prepare and present continuous improvement projects to management. Comprehensive understanding of regulatory guidelines and can independently develop, write and execute methods, protocols, reports and other related documents. Complete all work in a timely manner. Perform peer review of testing data. Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner. Complete all reviews in accordance with required timelines. Communicate effectively with peers, and demonstrate teamwork, with regards to results of review and corrections required. Participate in complex projects and continuous improvement efforts. Communicate effectively with management regarding task completion, roadblocks, and resource needs. Demonstrate initiative, courage, and continuous improvement throughout investigation/corrective action lifecycles. Required Qualifications: Education And Experience: Required B.S. with 2 years' work experience or M.S. with 0 years' experience in Molecular & Cellular Biology, Immunology, or related discipline. Advanced hands-on experience with various analytical techniques including flow-cytometry, molecular techniques Scientific knowledge in the characterization and transfer of pharmaceutical products. Experience with PCR and/or flow cytometry and/or mammalian cell culture is required. Experience working in a regulated (GLP/GMP) environment in preferred. Assay development, especially cell-based potency assays are preferred. Assay qualification/validation experience is preferred. Assay Technology Transfer (TT) experience is preferred. Excellent organization skills and ability to handle multiple tasks Highly motivated, willingness to acquire new skills, and ability to work with minimal supervision. Excellent verbal and written communication skills. Advanced problem-solving ability/mentality, technically adept and logical thinking. Ability to represent the interests of the group on cross-functional teams. Ability to work independently in a high-paced team environment, meet deadlines, and prioritize work from multiple projects. Ability to work with management locally and globally. Advanced ability to communicate effectively with peers, department management and cross-functional peers. Pay Rate: $49.13-$52.11/Hour If hired, you will enjoy the following ECLARO Benefits: 401k Retirement Savings Plan administered by Merrill Lynch Commuter Check Pretax Commuter Benefits Eligibility to purchase Medical, Dental & Vision Insurance through ECLARO If interested, you may contact: June Binuya junethel.binuya@eclaro.com 2128047476 June Binuya | LinkedIn Equal Opportunity Employer: ECLARO values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status, in compliance with all applicable laws.

You're a good fit if you: - Hold a PhD (or equivalent doctoral degree) in Clinical Research, Chemistry, Biology, Biochemistry, Molecular Biology, Pharmacology, or a related field - Received your undergraduate degree in US/UK/Canada/Western Europe - Received your graduate degree at a top US/UK/Ca

What we're looking for: - Professional experience in molecular & cellular biology techniques, experimental design & lab research, data analysis in life sciences - Strong communication skills - Ability to work independently in a remote environment How it works: This is not a specific job postin

Our partner labs are building models that need to reason about molecular biology, biophysics, structural biology, immunology, neuroscience, genomics, and adjacent disciplines at the level of a working researcher — not a textbook. We are recruiting a select cohort of accomplished biology and biophy

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Job Description About The Role The Genetics Lab Specialist I supports daily operations in the genetics laboratory by performing molecular laboratory procedures related to preimplantation genetic testing by next-generation sequencing. This position is responsible for accurate sample handling, preparation, documentation, and testing support in accordance with established laboratory procedures and quality standards.The Genetics Lab Specialist I works under the guidance of senior laboratory staff and management to ensure clinical samples are processed accurately, efficiently, and in compliance with laboratory policies. Responsibilities ● Perform assigned aspects of preimplantation genetic testing by next-generation sequencing, including DNA amplification, library preparation, sequencing setup, and reporting support. ● Perform molecular-based laboratory procedures on clinical samples in accordance with approved standard operating procedures. ● Accession clinical samples, including sample reception, verification, labeling, documentation, and logging. ● Ensure proper sample identification, tracking, handling, and storage throughout the testing process. ● Prepare reagents, consumables, and materials needed for laboratory workflows. ● Assist with operation, cleaning, and routine maintenance of laboratory instruments and equipment. ● Accurately document laboratory activities, test steps, reagent use, sample status, and any deviations from standard procedures. ● Assist with Quality Assurance, Quality Control, and Quality Inventory activities, including QC checks, inventory tracking, reagent monitoring, and documentation review. ● Maintain a clean, organized, and safe laboratory work environment. ● Follow all laboratory safety procedures, HIPAA requirements, and applicable compliance standards. ● Communicate sample issues, testing concerns, or workflow delays to senior staff or laboratory management. ● Participate in training and competency activities as required. ● Perform additional duties or assignments as directed by management. Who You Are ● Bachelor’s (or Master’s) degree in Biology, Molecular Biology, Genetics, Biochemistry, Medical Laboratory Science, or a related scientific field preferred. ● Previous experience in a clinical, molecular, genetics, IVF, or reproductive genetics laboratory preferred but not required. ● Experience with molecular biology techniques such as pipetting, PCR, DNA amplification, or sequencing preparation is preferred. ● Must know how to pipette small amounts by viscosity. ● Familiarity with next-generation sequencing workflows. ● Familiarity with laboratory documentation, sample accessioning, and quality control practices is preferred. ● Strong attention to detail and accuracy. ● Ability to follow written procedures, protocols, and laboratory instructions. ● Good organizational and time-management skills. ● Ability to work both independently and as part of a team. ● Strong communication skills and willingness to ask questions when clarification is needed. ● Ability to handle confidential patient and clinical information appropriately. ● Basic troubleshooting and problem-solving skills. ● Comfortable working in a fast-paced clinical laboratory environment. Physical and Work Environment Requirements ● Ability to work in a clinical laboratory environment with biological specimens, reagents, and laboratory equipment. ● Ability to sit or stand for extended periods of time. ● Ability to perform repetitive pipetting and other fine-motor laboratory tasks. ● Must be able to wear required personal protective equipment. ● May require occasional weekend, holiday, or adjusted schedule coverage based on laboratory needs.

Job Description SOKOL GxP Services is seeking a motivated Cell Therapy Analytical Development (CTAD) Analyst to support analytical testing and method transfer activities within a fast-paced cell therapy environment. This role supports process characterization testing for lentiviral vector and cell therapy drug product samples and requires hands-on laboratory experience in regulated pharmaceutical or biotechnology settings. Requirements • Perform analytical experiments using methodologies such as PCR, RT-qPCR, flow cytometry, mammalian cell culture, ELISA, MSD, and Luminex, • Execute GLP analytical testing to support process characterization activities, • Support analytical method transfer and assay execution with moderate supervision, • Analyze, summarize, and report experimental data accurately and compliantly, • Maintain laboratory documentation in accordance with GLP/GDP requirements, • Collaborate cross-functionally with Analytical Development and Quality teams, • Support assay qualification/validation and analytical troubleshooting activities, • Ensure proper operation and routine maintenance of laboratory equipment, • Participate in continuous improvement initiatives and support investigation activities as neededRequired Qualifications, • Bachelor’s degree in Molecular Biology, Cell Biology, Immunology, or related scientific discipline, • Minimum 2 years of laboratory experience in pharmaceutical, biotechnology, or cell therapy environments, • Hands-on experience with PCR and/or flow cytometry and/or mammalian cell culture, • Experience working in a GLP/GMP-regulated environment, • Strong scientific, analytical, and organizational skills, • Ability to work independently and manage multiple priorities in a fast-paced environment, • Strong written and verbal communication skillsPreferred Qualifications, • Experience with assay development or assay qualification/validation, • Cell-based potency assay experience, • Experience supporting analytical technology transfer activities, • Familiarity with lentiviral vector or cell therapy products Benefits Competitive hourly rate: $44.50 – $48.10/hr (W-2 only, no C2C) Working Hours: Monday - Friday, regular business hours 12-month contract with possible extension Health insurance, holiday pay, 401(k) program, and other benefits Employee referral bonus program

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