Research Associate II - Assay Development
Listed on 2026-10-08
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Research/Development
Research Scientist, Biotech Research, Research Assistant/Associate, Clinical Research
Job Title:
Research Associate II Assay Development Job Description
The Research Associate II in Assay Development conducts research, development, and manufacturing laboratory experimentation to support assay-related projects. This role designs, executes, and interprets experiments, prepares technical documentation, and contributes technical expertise to project strategies while ensuring full compliance with laboratory quality standards and procedures.
Responsibilities- Design and execute experimental protocols with minimal supervision, including making detailed observations and analyzing data to support assay development projects.
- Prepare and present clear technical reports, summaries, protocols, and quantitative analyses to project teams and stakeholders.
- Maintain complete, accurate, and compliant laboratory documentation in alignment with internal policies and quality systems such as GMP, GLP, and Design Control.
- Troubleshoot experimental and process-related problems, identify root causes, and implement effective corrective actions.
- Work collaboratively in a team environment, providing creative scientific input and contributing to project planning and strategy.
- Offer process improvement suggestions that enhance efficiency, quality, and reproducibility of laboratory work.
- Assist in identifying patentable inventions and innovative approaches arising from experimental work.
- Train colleagues on laboratory techniques, procedures, and documentation practices, and monitor their work to ensure quality and adherence to the Quality First Time principle.
- Exercise sound judgment in selecting appropriate methods, techniques, and tools to solve complex technical problems.
- Search and review relevant scientific literature to inform experimental design, optimize methodologies, and stay current with advances in the field.
- Use word processing, spreadsheet, and presentation software to organize data, prepare documentation, and communicate findings effectively.
- Bachelors degree in Life Sciences or a closely related discipline.
- 24 years of relevant post-college laboratory experience in research, development, or manufacturing environments.
- Proficiency in wet laboratory techniques, including accurate pipetting and the use of laboratory equipment such as balances and stir plates.
- Ability to conduct experiments independently, record observations meticulously, and analyze quantitative data.
- Strong capability to search and interpret scientific literature to support experimental design and problem-solving.
- Skilled in using word processing, spreadsheet, and presentation software for data analysis, documentation, and reporting.
- Good verbal and written communication skills, with the ability to present technical information clearly to diverse audiences.
- Meticulous attention to detail in experimental execution, data recording, and documentation.
- Coachable and receptive to feedback, with a demonstrated willingness and ability to learn new techniques and processes.
- Collaborative working style with a proven ability to contribute effectively within cross-functional teams.
Skills & Qualifications
- Experience working within GMP and GLP laboratory environments and familiarity with Design Control processes.
- Exposure to SAFe or Agile planning processes and reporting frameworks in a scientific or technical setting.
- Demonstrated ability to suggest process improvements and contribute to continuous improvement initiatives.
- Experience training peers or junior staff in laboratory procedures and documentation standards.
- Ability to identify potential patentable inventions or innovative methodologies arising from laboratory work.
This is an onsite laboratory position focused on assay development within a research and development environment. The role involves regular hands-on work in a wet lab setting, using equipment such as pipettes, balances, and stir plates, and adhering to GMP, GLP, and Design Control quality systems. Work is conducted in a structured, process-driven environment that emphasizes accuracy, documentation integrity, and the Quality First Time principle.
Team members collaborate closely, share results and insights, and participate in Agile-style planning and reporting where applicable. Standard professional laboratory attire is expected, with appropriate safety practices and protective equipment used as required by laboratory protocols.
This is a Contract position based out of Oro Valley, AZ.
Pay and BenefitsThe pay…
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