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Molecular Technologist I-IIITempus • Minneapolis, Minnesota, United States
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Molecular Technologist I-III

Tempus
  • US
    Minneapolis, Minnesota, United States
  • US
    Minneapolis, Minnesota, United States
Jetzt Bewerben

Über

Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. Position Overview OneOme is seeking a Molecular Technologist to work closely with laboratory staff and cross-functional teams in support of our pharmacogenomics testing operations in Minneapolis. This role is responsible for several phases of the testing workflow, including sample accessioning, DNA extraction, real-time PCR, and data analysis. The Molecular Technologist performs high-complexity clinical molecular testing in accordance with established procedures, quality standards, and regulatory requirements. In addition to routine clinical testing, this position will contribute to assay development and validation, quality assurance and quality control activities, and other laboratory initiatives as assigned. The ideal candidate will bring strong technical expertise, excellent attention to detail, effective communication skills, and the ability to work both independently and collaboratively in a fast-paced environment. This role is expected to support operational needs that include weekend shifts. Responsibilities
Perform sample accessioning, DNA extraction, PCR testing, and data review according to standard operating procedures
Conduct high-complexity clinical molecular testing in compliance with applicable regulatory and quality standards
Perform quality control and quality assurance activities, including maintenance of
associated records, monthly and annual reviews, and internal audits
Support laboratory development activities, including new method and assay development, workflow and process optimization, analytical validations, and software verification testing
Develop written technical and scientific content for procedures, policies, whitepapers, and peer-reviewed publications
Assist as needed with non-laboratory functions, including clerical duties, inventory control, client service activities, and other assigned responsibilities
Collaborate effectively with laboratory staff and other departments to support operational excellence
Maintain flexibility to support scheduled weekend coverage as needed
Required Qualifications
Master's or Bachelor's degree in medical technology, clinical laboratory science, or a related chemical, physical, or biological field
Educational background from an accredited institution totaling at least 60semester hours, or equivalent, from an accredited institution that, at a minimum, includes either:
24 semester hours of medical laboratory technology courses; or 24 semester hours of science courses that include: 6 semester hours of chemistry; 6 semester hours of biology; and 12 semester hours of chemistry, biology, or medical laboratory technology in any combination. Minimum of 1 to 2+ years of post-baccalaureate (post-BS degree) clinical experience within a high-complexity CAP/CLIA-certified laboratory environment At least 6 to 12 months of hands-on expertise in molecular techniques, including nucleic acid extraction
Excellent communication skills
Ability to work with others to plan and carry out scientific programs.
Self-driven and works well in an interdisciplinary team with minimal direction
Strong desire to build products that will save lives and change the course of patient care
Impeccable attention to detail.
Preferred Qualifications
ASCP certification, or eligibility for certification in a related specialty
Prior experience in a CLIA laboratory environment
4 years+ of experience performing high-complexity testing
Experience with laboratory automation and liquid handling systems, in-house assay development, and validation activities including primer and probe design, assay optimization, and troubleshooting
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
  • Minneapolis, Minnesota, United States

Sprachkenntnisse

  • English
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