Labcorp is a global leader in diagnostic testing and drug development solutions, helping healthcare providers, researchers, and patients make informed decisions that advance care. Join us in our mission to improve health and improve lives. Labcorp is seeking a Scientist II Clinical Genomics to join our team in Iselin, NJ! Work Schedule: This is a 1st shift position primarily onsite due to the hands-on laboratory responsibilities with occasional remote work opportunities for documentation, data analysis, or planning activities. Position Summary:We are seeking an initiative-taking and technically skilled Assay Development and Validation Scientist to join our clinical genomics laboratory. This role is heavily focused on hands-on laboratory work, with the primary responsibility centered on the technical execution of complex R&D experiments, design and execution of validation studies, and continuous improvement of existing assays and workflows. The ideal candidate will bring deep expertise in next-generation sequencing (NGS) and other high-complexity genomic technologies, along with strong analytical and technical writing capabilities. Minimum Qualifications: PhD. in Molecular Biology, Genetics, or Biochemistry or Bachelor of Science degree with 4 or more years of experience in a clinical, diagnostic, or GMP-regulated laboratory . or more years of experience with Next-Generation Sequencing (NGS) technologies and workflows . or more years of experience with genetic testing methodologies (PCR, q. PCR, dd. PCR, microarrays, or library preparation techniques). Preferred Qualifications 1 or more years of experience with assay validation, method comparison, and performance qualification studies in a regulated environment (CLIA, CAP, or GMP).1 or more years of experience supporting assay transfer, scale-up, or commercialization efforts. Additional Job Standards:Ability to demonstrate exceptional technical writing skills, with experience in preparing validation plans, reports, and SOPs. Ability to effectively analyze, problem-solve and design experiments. Ability to effectively demonstrate a high attention to detail, quality, and regulatory compliance. Ability to manage multiple projects and priorities in a fast-paced environment. Ability to effectively communicate and collaborate across cross-functional teams. Pay Range: $90 k - $129 k annual (USD)All job offers will be based on a candidates skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/ LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please click here.