Molecular Technologist I-III

Oneome - Intercompany Costing Company; Minneapolis (MN); On-site; USD 60,000 - 80,000; Full time

Job summary

Oneome - Intercompany Costing Company in Minneapolis is looking for a Molecular Technologist to support pharmacogenomics testing operations. The role involves tasks such as DNA extraction, real-time PCR, and data analysis, all while ensuring quality in compliance with regulations.

The ideal candidate will have a relevant degree, clinical lab experience, and the ability to work effectively in teams. This position offers the chance to make significant impacts on patient care through precision medicine.

Qualifications

• Minimum of 1 to 2+ years of clinical experience in high-complexity laboratory.
• Hands-on expertise in molecular techniques, including nucleic acid extraction.

Responsibilities

• Perform DNA extraction, PCR testing, and data review.
• Conduct quality control and assurance activities.
• Support laboratory development activities and collaborations.

Skills

Excellent communication skills

Attention to detail

Team collaboration

Molecular techniques expertise

Education

Master's or Bachelor's degree in medical technology or related field

Job description

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.

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, white papers, 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 60 semester hours, or equivalent, 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 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.

Equal Opportunity Employer

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.