Scientist Bioscience - ELISA

Scientist Bioscience - ELISA

Location: Gaithersburg, MD

Onsite Flexibility: Hybrid 100% onsite for the first 2 3 months, then hybrid

Contract Details

• Position Type: Contract
• Contract Duration: 12 months
• Pay Rate: $38.00 $42.00 / Hour (USD)
• Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Job Summary

This role focuses on coordinating samples and performing routine laboratory testing in support of cell therapy programs. The position involves executing assays such as flow cytometry, ELISA, or molecular assays, depending on training and assignment. The scientist will use both manual and automated testing methods and learn automated data systems for reporting results. The role also supports automation work, general lab maintenance, equipment and reagent upkeep, and continuous-improvement projects. The team is collaborative and communicates regularly about schedules, priorities, and project updates.

Key Responsibilities

• Perform routine analytical testing of cell therapy in-process samples using methods such as flow cytometry, ELISA, cell-based cytotoxicity assays, and digital PCR.
• Prepare samples, reagents, controls, and materials in accordance with approved procedures and laboratory practices.
• Generate accurate, reliable, and timely analytical data while maintaining complete and well-organized laboratory documentation.
• Coordinate test sample receipt, scheduling, and prioritization with the cross-functional team.
• Communicate test status, results, observations, and potential issues clearly to project teams.
• Support process scale-up, technology transfer, troubleshooting, and continuous-improvement activities by generating data and completing assigned experimental tasks.
• Follow established procedures, laboratory safety requirements, and applicable quality standards.
• Assist with investigation of unexpected results and contribute to identifying opportunities to improve testing workflows and laboratory operations.
• Collaborate effectively in a fast-paced, cross-functional environment and manage multiple testing activities according to project priorities.

Education Requirements

• Master's degree or equivalent in biology, biochemistry, biotechnology, cell biology, molecular biology, or a related scientific field.
• A bachelor's degree with approximately 2 3 years of relevant hands-on experience is acceptable; internships may count.

Required Experience

• Two years of relevant laboratory experience.
• Experience working in a laboratory environment with biological samples and standard laboratory equipment.
• Hands-on laboratory experience and a practical understanding of how lab testing is performed.
• Experience executing routine testing methods.
• Candidates should have enough lab experience to contribute without needing training in basic laboratory practices.
• Candidates with more than 10 years of experience may be overqualified for the level of the role.

Nice-to-Have Experience

• Flow cytometry and/or ELISA experience is preferred; experience with one of these may be sufficient.
• Industry experience, such as QC or in-process testing, is preferred but not required.

Required Skills

• Ability to follow written procedures, accurately document experimental work, and communicate results effectively.
• Strong organizational skills and the ability to manage multiple priorities in a fast-paced setting.
• Strong communication skills, including willingness to speak up, report issues, and ask questions.
• A willingness to learn and adapt to the team's methods and processes.

Benefits

• Medical, Vision, and Dental Insurance Plans
• 401k Retirement Fund

Important Notes

• Interview process: 1 onsite panel interview.

About the Client

This client is a biopharmaceutical and life sciences organization with operations across strategic U.S. locations including the greater Washington, D.C. area and Southern California, focused on advancing cell therapy and biologics programs. The organization employs scientists, quality assurance specialists, R&D professionals, and regulatory affairs experts who collaborate across research, development, and manufacturing functions. Contract-based roles offer exposure to cutting-edge cell therapy development within a corporate pharma environment that adheres to rigorous GMP/cGMP and GxP regulatory standards.

About GTT

GTT is an NMSDC-certified Minority Business Enterprise (MBE) headquartered in Portsmouth, New Hampshire. GTT is a subsidiary of Chenega Corporation, an Alaska-based company and one of the largest Alaska Native-owned corporations. An Inc. 5000 honoree and one of SIA's Best Staffing Firms to Work For, GTT connects professionals with Fortune 500 organizations across IT, engineering, construction, utilities, life sciences, financial services, and healthcare throughout the U.S. and Canada. We're committed to diverse, inclusive workplaces and to placing people in roles where they can do their best work.

Job Number: 26-18255

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