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Molecular Technologist III - Team Lead (2nd shift)

Biofidelity

Biofidelity

Morrisville, NC, USA
Posted 6+ months ago
Biofidelity is a revolutionary genomic technology company dedicated to unleashing the potential of genomics to transform human health and the world we live in. Our adaptive platform technology removes the noise from genomic data, providing only the information needed to make decision making less complex, faster, and more accurate.
At Biofidelity we are proud to have built a culture of humanity, openness and high expectations. We work towards well-defined goals, with a strong belief that we can make genomics globally accessible. Our people are keen to take responsibility for their work and share both their successes and challenges.
Alongside a competitive salary and opportunities for career development, we offer a comprehensive benefits package including medical, dental and vision coverage, 401(k), bonus, stock options, life insurance, short-term and long-term disability income protection, 20 days per year PTO allowance and 2 floating holidays in addition to Company observed holidays.
The role
Biofidelity is seeking a Molecular Technologist III to perform high complexity diagnostic testing using Biofidelity’s ASPYRE technology, histology, and nucleic acid extraction workflows. With minimal oversight from the Supervisor, the Molecular Technologist III will be responsible for the efficient and quality execution of sample accessioning, processing, data generation, and reporting in the clinical laboratory. The ideal candidate has strong molecular biology technical skills, is collaborative, trustworthy with ability to work in a fast-paced clinical environment. This role reports to the Director of Operations (CLIA/CAP).
The schedule for this position will be: Monday-Friday, 3pm-11:30pm with shift differential offered.
Key responsibilities:
Performs the following with high proficiency: specimen receipt and accessioning, histology, and all high complexity molecular functions including nucleic acid extraction, quantification, and normalization; PCR; and qPCR
Performance, assessment, and planning of reagent preparation, equipment maintenance, and quality control checks
Communicate and collaborate with other technologists, laboratory leadership, and customer service to ensure high-quality processing and results
Responsible for the adoption and validation of new methodologies, including evaluating and establishing novel workflows, instrumentation, and protocols
May assume full responsibility for one or more laboratory projects or functions, such as: safety, quality control, regulatory compliance, administrative tasks, staff development, or computer systems
Provide high complexity testing, process, histology, and other lab training to new employees
Author, revise, and update SOPs as required by regulations and process improvements
May perform quality assurance checks on clinical and testing documentation and analytical results in preparation for clinical report generation
Performs analytical analysis and report generation for Lab Director review and sign-out
Independently identify and troubleshoot advanced specimen acceptability or assay issues
Act as a consultant for troubleshooting high complexity problems in multiple areas of the laboratory and/or administrative workflow
Engage in cross-functional projects involving teams such as Customer Service, Commercial, Computational, People, Technology and Product Development
Other duties as assigned
Knowledge, Skills and Abilities:
Advanced experience with nucleic acid extractions, PCR, qPCR, NGS, basic histology, and SOP writing
Experience with HIPAA, CLIA, CAP, or other regulatory audits and compliance
Experience in planning, authoring, or greatly assisting analytical, process, or software validations
Experience in researching and implementing new instrumentation, assays, or protocol improvements
Ability to identify and solve complex analytical issues
Experience in training coworkers to perform high complexity testing
Demonstrated excellence in teamwork, cross-functional collaboration, and mentorship
Demonstrated leading role in cross-functional projects
Experience with Word, Excel, Google Suite, and Laboratory Information Management Systems (LIMS)
Excellent written and verbal communication skills
Excellent attention to detail and organizational skills
Requisite Education and Experience / Minimum Qualifications:
Bachelor’s degree in medical laboratory science or biological or chemical sciences with >3 years molecular laboratory work experience in a CLIA/CAP-regulated lab, OR
Master’s degree in medical laboratory science or biological or chemical sciences with >2 years experience (preferred)
ASCP-MLS, ASCP-MB, AMT-MT, AMT-MDT, or similar certification (strongly preferred; required within 1 year of hire)