Senior Lab Technician: Molecular Diagnostics (PCR/NGS)

Every team member at Biodesix has the potential to impact our business and our patients, providers, and partners. Even our company logo includes a “thumbprint” – a visual reminder that encourages all team members to put their fingerprints on our future. Explore our openings below and see if your next role is here with Team Biodesix. Thank you for considering us in your search. Position: Laboratory Technician III Location: Louisville, CO Job Id: 809-050044 # of Openings: 1 ABOUT US: Biodesix is a leading diagnostic solutions company, driven to improve clinical care and outcomes for patients. Biodesix Diagnostic Tests support clinical decisions to expedite personalized care and improve outcomes for patients with lung disease. Biodesix Development Services enable the world’s leading biopharmaceutical, life sciences, and research institutions with scientific, technological, and operational capabilities that fuel the development of diagnostic tests, tools, and therapeutics. Our Mission: Transform patient care and improve outcomes through personalized diagnostics that are timely, accessible, and address immediate clinical needs. Our Vision: A world where patient diseases are conquered with the guidance of personalized diagnostics. Senior‑level, experienced Laboratory Technician III to assist with the setup and support of the daily activities of our Colorado BSL2+ laboratory. The Laboratory Technician III has the technical training and experience required to perform minimally supervised clinical laboratory testing (test specimen receipt through test result generation) using standard in‑vitro laboratory techniques in polymerase chain reaction (PCR), next generation sequencing (NGS) and in Mass Spectrometry (MALDI‑ToF and/or LC/MS). Our focus areas of test development in lung diseases with a focus on pulmonology and oncology. This experienced candidate is comfortable with SOPs and Work Instructions, with working with data, standard laboratory chemicals, human blood specimens and is versed in standard molecular and analytic techniques (sample preparation, PCR, nucleic acid isolation/purification and sequencing). This position works in a functional matrix organization, including in Product Development Core Teams and with departments including Customer Service, Finance/Accounting, Quality management team, the Laboratory Directors, Business Development, CDMA, and other departments as needed. Trouble shooting, data analysis, and report creation are required roles for this position. Appropriate designees may act as responsible delegates according to the establishing Roles and Responsibilities, including day to day responsibilities required for CAP/CLIA, NYS CLEP, as well as all state‑specific requirements in which Biodesix is an approved test facility. This is an on‑site laboratory role. REGULATORY REQUIREMENTS This role shall comply, at a minimum, with the responsibilities and qualifications outlined in: CLIA: Clinical Laboratory Improvement Amendments (CLIA) Requirements, Title 42 Code of Federal Regulations Part 493 CAP: College of American Pathologists (CAP): All Common, General, Director Responsibility and Authority and all test‑specific checklists NYS CLEP: New York State Department of Health, Clinical Laboratory Evaluation Program (CLEP), New York State Public Health Law, Article 5 Title 5 ISO: International Organization for Standardization (ISO) 13485, Quality Management Systems, Requirements for Regulatory Purposes, 2016 All other applicable state and regulatory governing authorities including but not limited to: CA, PA, RI, MD RESPONSIBILITIES Completes training and Competency Assessment for all new and existing procedures Takes responsibility for completing continuing education requirements set by applicable regulatory and accrediting agencies Performs all test realization function in support of Biodesix products and services Performs product test support for incoming raw materials in support of Biodesix products and services Trouble shooting and data analysis Skilled in the use of the Quality Management System for document management and reviews. Creates product improvement plans, executes studies according to protocols, completes report in QMS Performs duties in line with established SOP Uploads appropriate data to the Customer Service team. Contributes to the overall maintenance of laboratory equipment and supplies following SOPs Contributes to the creation and revision of Laboratory SOP in the QMS Contributes to the Internal Audit readiness through good documentation practices Performs all job functions in accordance with HIPAA Contributes to new Product Development projects, including in product transfer to Laboratory Operations Communicates effectively with on‑site and remotely located management/support teams. Works independently and has exceptional written and verbal skills SME, technical support representative for service calls Other duties as assigned. COMPETENCY OR POSITION REQUIREMENTS Outstanding technical laboratory skills Participate in CE program Proficient in the use of the Quality Management System for document management and reviews Knowledge of lab safety Excellent attention to detail with a strong commitment to thoroughness and error‑free execution of procedures Exceptional organizational and documentation skills Basic computer skills required (Word, Excel, PowerPoint) Ability to work well as an individual and as a team member Very strong work ethic Competency in Microsoft Office (SharePoint, Teams, Word, Excel, PowerPoint) Bachelor’s of Science degree in a chemical, physical, biological or clinical laboratory science or medical technology At least 3 years in a high complexity lab with molecular biology/chemistry/virology/immunology training. Will be expected to perform testing in a BSL2+ regulated Laboratory. Technical supervisory experience a plus. Expert in working in BSC and with PCR methods WHAT YOU'LL GET Compensation rate starting at $32.00 per hour Discretionary Bonus opportunity Comprehensive health coverage: Medical, Dental, and Vision Insurance: Short/Long Term Disability and Life Insurance 120 hours of annual vacation 72 hours of paid sick time off 11 paid holidays + 3 floating holidays Employee Assistance Program Voluntary Benefits Employee recognition program Biodesix is 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, disability, or veteran status. Biodesix is proud to be an Equal Opportunity Employer We are committed to ensuring an inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Notice to Recruitment Agencies In the case of candidates submitted or presented to Biodesix by a recruiter or agency without a signed agreement, Biodesix explicitly reserves the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency. Accommodation Notice If you are an individual with a disability and require a reasonable accommodation to use our online system to search and/or apply for a position, please send us an email at View email address on click.appcast.io. #J-18808-Ljbffr