Laboratory Manager

Location: Onsite in Boulder, CO

About the Company:

Foresight Diagnostics is a molecular diagnostics company advancing non-invasive cancer detection through highly sensitive, cell-free DNA–based liquid biopsy technologies. Our proprietary methods, originally developed at Stanford University, are designed to enable earlier detection of smaller tumors and support more personalized, effective cancer treatment strategies.

We operate at the intersection of molecular biology, bioinformatics, and next-generation sequencing (NGS), translating rigorous scientific innovation into clinically meaningful solutions. As our organization has grown, we have built robust laboratory operations, cross-functional collaboration, and scalable processes to support clinical development and long-term commercial readiness.

Foresight Diagnostics offers a collaborative, high-accountability work environment where quality, precision, and continuous improvement are core to how we operate. Team members have the opportunity to contribute to impactful programs, work alongside experienced scientific and operational leaders, and grow professionally within a well-resourced and mission-focused organization. Foresight Diagnostics is headquartered in Boulder, Colorado.

About the Role:

The Laboratory Manager (Tuesday-Saturday) at Foresight Diagnostics oversees the daily operations of the Laboratory Services function across both clinical and translational research work-streams. Working closely with the Director, Clinical Laboratory Operations and the Laboratory Manager (Monday-Friday), this position is responsible for managing personnel, maintaining and optimizing lab workflows, ensuring compliance with quality and regulatory standards, and fostering a culture of excellence and safety within the laboratory environment. The Laboratory Manager (Tuesday-Saturday) collaborates with cross-functional partners to drive smooth day-to-day operations and high-quality execution of cancer diagnostic testing. A successful candidate will possess a strong blend of technical expertise in NGS workflows, leadership skills, regulatory knowledge, and practical experience in laboratory operations. This is a full-time onsite role in a Tuesday-Saturday work schedule, with occasional flexibility for evening, weekend, or holiday work as operational needs arise. This role reports to the Director, Clinical Laboratory Operations.

What You Will Do:

Operational Support and Workflow Coordination

• Maintain proficiency in wet-lab techniques and provide training or bench support as needed, while primarily functioning in an oversight and decision-making capacity.

• Ensure appropriate technical coverage, training, and escalation support across shifts. Accountable for meeting turnaround time (TAT), quality, and productivity targets.

• Under delegation from the Laboratory Director, review and release patient reports, ensuring activities are performed in accordance with regulatory and quality standards.

• Proactively monitor laboratory performance metrics, identify risks to quality or turnaround time, and implement corrective and preventive actions as needed.

• Provide leadership and oversight of instrument maintenance programs, troubleshooting workflows, and calibration activities. Ensure appropriate escalation, cross-functional engagement, and documentation for equipment-related issues.

• Collaborate with the Supply Chain team to track inventory, verify shipments, and maintain adequate stock of supplies and reagents. Ensure proper storage, labeling, and reagent lifecycle management to minimize waste and prevent operational disruption.

• Partner with the Director, Clinical Laboratory Operations and laboratory management to implement and maintain efficient workflows, ensuring consistency and adherence with established procedures. Lead identification and execution of process improvements that enhance efficiency, scalability, quality, and cost effectiveness.

• Lead operational readiness and response for contingencies such as equipment downtime, staffing gaps, or workflow interruptions. Oversee root cause investigations, documentation, and implementation of corrective actions following operational incidents.

Personnel Support

• Hold direct supervisory responsibility for laboratory personnel, including performance management, engagement, and professional development.

• Establish clear performance expectations and provide ongoing coaching, feedback, and formal evaluations. Address performance concerns proactively and in alignment with HR and organizational policies.

• Under guidance of the Director, Clinical Laboratory Operations, support recruiting, hiring, onboarding, and retention efforts to build a high-performing, collaborative laboratory team.

• Ensure robust training programs are in place and that staff maintain competency across required assays, systems, and regulatory expectations. Oversee training documentation and competency assessment programs.

• Foster a culture of accountability, continuous improvement, and patient-focused quality. Serve as an accessible leader and escalation point for team concerns and operational challenges.

Cross-Functional Support

• Represent the laboratory in cross-functional initiatives and planning discussions. Advocate for operational needs, resource planning, and workflow considerations in broader organizational decisions.

• Coordinate effectively with cross-functional teams such as Operational Excellence, Clinical Operations, Quality Assurance, Bioinformatics, Assay Development, Supply Chain, and Facilities to ensure alignment and smooth execution of shared processes.

• Provide clear, timely communication to internal stakeholders regarding operational status, risks, changes in capacity, or process updates.

• Escalate strategic or high-risk issues to the Director, Clinical Laboratory Operations and Laboratory Director with proposed mitigation strategies.

Quality & Compliance

• Partner with the Laboratory Director and Director, Clinical Laboratory Operations to ensure full compliance with CLIA, CAP, FDA, GxP, and other applicable regulatory and accreditation standards.

• Oversee execution and review of quality control programs, proficiency testing, and quality metrics. Ensure appropriate documentation, trend review, and follow-up actions.

• Lead laboratory inspection readiness efforts and support responses to audits, inspections, and regulatory inquiries.

• Ensure a strong culture of safety and regulatory compliance. Oversee implementation of laboratory safety programs, adherence to OSHA and internal policies, and timely reporting and investigation of safety incidents.

What You Will Bring:

• Bachelor's (BA/BS), Master’s (MA/MS), or PhD/MD in a relevant scientific field such as biology, chemistry, medical technology, laboratory management or a related discipline required.

• Certification as a Medical Laboratory Scientist (MLS), Clinical Laboratory Scientist (CLS), or equivalent certification, and licensure in California is required.

• Qualified to receive delegation as a General Supervisor in New York and California (combination of education and years of experience in high complexity clinical testing).

• Minimum of 3 years of experience in people leadership roles within laboratory and operations environments.

• Excellent leadership, team management, and interpersonal skills with the demonstrated ability to lead and manage a diverse team of laboratory professionals, influence cross functional teams, and operate as a change champion.

• Proficiency in a wide range of laboratory techniques and procedures relevant to high complexity testing, including molecular biology and next generation sequencing.

• Experience with the operation, maintenance, and troubleshooting of laboratory instruments and equipment used for high complexity testing.

• Knowledge of quality control principles and practices, including the implementation and interpretation of quality control procedures, proficiency testing, and documentation requirements.

• Understanding of CLIA regulations and guidelines, ISO15189, as well as other relevant regulatory requirements such as FDA regulations, Good Laboratory Practices (GLP), and Good Clinical Practices (GCP) requirements.

• Ability to analyze and interpret laboratory data, identify trends or deviations, and take appropriate corrective actions as needed.

• Excellent organizational skills with experience in laboratory workflow optimization.

• Ability to support strategic plans, goals, and objectives for the laboratory, aligning with the organization's mission and objectives.

• Self-starter with the ability to thrive in a fast-paced, ambiguous environment and deliver projects autonomously.

Compensation & Benefits

This role is hiring at an annual salary of $125,000 - $140,000 and is eligible for bonus and equity offerings. Foresight offers benefits including paid vacation, sick time, and parental leave (if applicable), alongside medical, dental, vision, life, disability coverage, flexible spending accounts, and a 401k with company match.

You will be working on interesting problems with extremely high impact. We promote the professional development of our employees and will encourage upward mobility within the company for high performing employees. Foresight Diagnostics is 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.