What are the responsibilities and job description for the Molecular General Supervisor position at Aura Genetics?
Aura Genetics is a high-complexity diagnostic laboratory servicing the booming at-home testing and wellness market, has teamed up with UPS Healthcare to build Aura’s new headquarters in Louisville, Kentucky. Aura’s main lab will be constructed at the end of the runway at the Louisville airport, giving Aura Genetics an unprecedented logistical advantage to provide test results faster.
Job Title: Molecular General Supervisor
Job Type: Full-time
Reports to: Laboratory Director / Technical Supervisor
Job Summary:
We are seeking a skilled and motivated Molecular General Supervisor to lead operations in our high-complexity PCR testing laboratory located in Louisville, KY. This role involves supervising day-to-day operations, overseeing high-throughput molecular diagnostics, and ensuring accuracy, efficiency, and compliance with regulatory standards. The ideal candidate has strong technical expertise with PCR platforms, sample prep automation, and experience supervising clinical lab personnel in a fast-paced environment.
Key Responsibilities:
Leadership & Daily Operations
- Provide direct supervision of testing personnel and daily oversight of molecular lab operations.
- Ensure efficient workflow and staffing coverage in a high-volume PCR environment.
- Set a professional example for lab staff and offer guidance, support, and technical mentorship.
PCR Testing & Technical Expertise
- Operate and maintain PCR instrumentation (Thermo QuantStudio or similar platforms).
- Review PCR data, validate results, and ensure accuracy in LIS reporting.
- Prepare 96- and 384-well plates with proficiency in pipetting and plate setup.
- Utilize sample prep automation (e.g., Tecan Fluent), volumetric glassware, and reagent preparation techniques.
- Adhere to biosafety level requirements and proper PPE usage when handling clinical specimens.
Quality Control & Compliance
- Monitor quality assurance programs to ensure compliance with CLIA, CAP, and OSHA standards.
- Perform and review calibrations, QC runs, and instrument maintenance.
- Investigate and resolve nonconformances and ensure corrective actions are taken and documented.
- Draft, revise, and enforce SOPs.
Personnel Management & Training
- Assist with onboarding, training, and competency assessments for new staff.
- Schedule and oversee continuing education and proficiency testing.
- Conduct annual performance reviews and ensure ongoing employee development.
Operational Support
- Monitor and maintain lab supply inventory, including reagents, chemicals, and PPE.
- Evaluate quality indicators such as turnaround time, rejected specimens, and error rates.
- Respond to client inquiries and complaints, and coordinate resolutions with lab leadership.
Qualifications & Requirements:
- Education & Certification:
- Bachelor’s degree in Medical Technology, Molecular Biology, Clinical Laboratory Science, or related field.
- Board certification as a Medical Technologist (ASCP or equivalent).
- Experience:
- Minimum 4 years of experience in a CLIA-certified clinical laboratory.
- Minimum 2 years in a supervisory or leadership role preferred.
- Hands-on experience with PCR testing and molecular diagnostics.
- Skills:
- Expertise in PCR platforms, sample prep automation, and molecular lab workflows.
- Excellent organizational, communication, and leadership skills.
- Strong knowledge of lab math, data interpretation, and quality management.
- Ability to adapt to high-pressure and fast-paced environments.
Benefits:
- Competitive salary (negotiable based on experience)
- Health insurance and 401(k)
- Employee profit-sharing program
- Relocation assistance
- Generous paid time off and holidays