Associate Scientist 2 - Assay R&D #4992

Our mission is to detect cancer early, when it can be cured. We are working to change the trajectory of cancer mortality and bring stakeholders together to adopt innovative, safe, and effective technologies that can transform cancer care. We are a healthcare company, pioneering new technologies to advance early cancer detection. We have built a multi-disciplinary organization of scientists, engineers, and physicians and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicine’s greatest challenges. GRAIL is headquartered in the Bay Area of California, with locations in Washington, D.C., North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies. For more information, please visit grail.com Responsibilities: Perform a range of established laboratory experiments using professional methods in molecular biology, including RNA isolation, genomic DNA isolation, cDNA preparation, cloning, fermentation, protein expression, and purification with increasing independence and accuracy. Prepare, process, and analyze samples, reagents, buffers, and media for experimental workflows while applying professional judgment to ensure precision, proper documentation, and procedural compliance. Collect, interpret, and document experimental data in laboratory notebooks or electronic systems using professional data management practices that support reproducibility and scientific integrity. Operate, maintain, and perform routine troubleshooting on laboratory equipment, identifying issues that require escalation and ensuring continuous readiness of instruments used in scientific work. Assist in refining laboratory protocols or methods by providing professional observations on workflow efficiency, data quality, and opportunities for procedural improvement. Contribute to the preparation of technical reports, data summaries, protocol drafts, and quantitative analyses to support scientific communication and project decision-making. Ensure adherence to safety, regulatory, and quality standards in the handling of chemical and biological materials, demonstrating accountability for maintaining a professional laboratory environment. Support laboratory operations through inventory oversight, organization of materials, coordination of supply needs, and contributions to continuous process improvements. Provide informal guidance and technical support to junior laboratory staff by sharing professional knowledge, reinforcing documentation standards, and modeling effective laboratory practices. These job duties are a summary of the primary duties and responsibilities of the job and position. It is not intended to be a comprehensive or all-inclusive listing of duties and responsibilities. Contents are subject to change at the company's discretion. Adaptability and Growth Expectation: As our organization continues to evolve and grow, this role may require flexibility in responsibilities and duties. Employees should expect that their role may expand, shift, or be modified to meet changing business needs, strategic priorities, and organizational objectives. This may include: Taking on additional responsibilities. Participating in cross functional projects and initiatives. Adapting to new technologies, processes, or methodologies. Supporting other departments or teams during periods of high demand. Contributing to special projects or temporary assignments as needed. Required Qualifications: Bachelor’s degree in Biology, Chemistry, Biochemistry, or related scientific discipline with 2–5 years of relevant experience; OR Master’s degree in a related field with 0–2 years of relevant experience. Demonstrated level of knowledge regarding applicable regulatory standards commensurate with the position's complexity and scope, contributing to organizational regulatory compliance. Minimal applicable standards for this position include: GMP quality management systems (e.g. ISO 13485) Operations within the regulated medical device environment (e.g. IVDD, IVDR, FDA 21 CFR 800 series, FDA 21 CFR Part 11) Preferred Qualifications: Solid technical proficiency in standard laboratory techniques and equipment operation. Ability to analyze data, identify issues, and communicate findings clearly. Strong organizational and problem-solving skills with attention to detail. Effective communication skills, both written and verbal. Ability to work both independently and collaboratively within a team environment. Familiarity with laboratory documentation systems, data management tools, and reporting processes. Knowledge of laboratory safety practices, compliance requirements, and quality standards. Physical Demands and Environment: Work is primarily performed in a laboratory environment with exposure to biological, chemical, or hazardous materials. Routine use of PPE including lab coats, gloves, and safety glasses is required. Involves prolonged periods of standing, pipetting, and handling laboratory materials. May occasionally require evening or weekend work to meet project demands. Operates under moderate supervision with periodic review of work products and outcomes.