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in Seattle, WA

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Hours Full-time, Part-time
Location Seattle, Washington

About this job

Seattle Every immune system has a story to tell— the key is knowing how to listen. Our goal is to meaningfully improve people’s lives by learning from the wisdom of their adaptive immune systems. It’s a bold objective that we’re uniquely built to achieve. At Adaptive, you'll be challenged, you'll be inspired, and you'll be part of an innovative organization making a real impact on improving the quality of life globally. No matter what your role is, you'll find a diverse, team-driven, fun culture where your contributions truly count. Position Overview The Assistant Clinical Molecular Genetics Laboratory Director will provide technical functions and support for CLIA/CAP regulated high complexity clinical laboratory performing molecular testing using NGS; and assist with maintenance of laboratory compliance. Responsibilities Reviews assay QC data for clinical patient testing, clinical trials and research studies Collaborates with the other Laboratory Staff to ensure timely and accurate result reporting Works with Project Management to support timely and smooth transfer of assays from R&D to the production laboratory Develops deep clinical and technical knowledge for all clinical assays in the production laboratory Monitor assay health and trouble-shoot assays that require quality improvement Provide clinical and technical expertise in support of new initiatives relevant to clinical and molecular testing Authors and/or reviews laboratory requirement documents (e.g., Analytic Methods, SOPs, and Analytic Validation Reports) Support s LIMS Development in collaboration with the software team (e.g., generates user requirements, UAT cases and plans, completes test plans, reviews and approves related documents for system features and enhancements) Collaborates with VP, Clinical Laboratory Director to develop and continuously improve day-to-day operations and ensure cross-functional alignment with laboratory support groups Support and initiate activities, in conjunction with the VP, Clinical Laboratory Director to ensure laboratory compliance with applicable regulations Upholds clinical laboratory best practices; and complies with applicable regulations Promotes a positive work environment while supporting management and business goals Requirements M.D. or Ph.D. in a biological science ABMGG, ABP, ABB, ABCC or equivalent laboratory director certification in Clinical Molecular Genetics/Pathology (Board-eligible may apply) Preferred Eligible to apply or holds a New York State Certification of Qualification in Oncology (Molecular Cellular Tumor Markers). Advanced critical thinking and problem solving skills Experience within regulated GxP laboratory environment Ability to collaborate across teams and disciplines Previous experience working with Next Generation Sequencing Platforms and bioinformatics High attention to detail Excellent organizational and time-management skills Superior oral and written communication skills Ability to multi-task and work in a fast-paced environment Adaptive Biotechnologies is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Equal Opportunity Employer/Veterans/Disabled NOTE TO EMPLOYMENT AGENCIES: Adaptive Biotechnologies values our relationships with our Recruitment Partners and will only accept resumes from those partners whom have been contracted by a member of our Human Resources team to collaborate with us. Adaptive Biotechnologies is not responsible for any fees related to resumes that are unsolicited or are received by any employee of Adaptive Biotechnologies who is not a member of the Human Resources team.