Exact Sciences · 4 hours ago
Supervisor, Pre-Analytical Laboratory - Tuesday to Saturday, 9am-5:30pm
Exact Sciences is a company focused on changing how the world prevents, detects, and guides treatment for cancer. The Supervisor, Pre-Analytical Laboratory is responsible for overseeing team members and daily operations in the Pre-Analytical department, ensuring compliance with policies and procedures while coordinating workflows and managing projects.
BiotechnologyHealth DiagnosticsManufacturingMedical
Responsibilities
Manage the daily operations of the pre-analytical laboratory department and ensure that all activities within department are performed and documented according to the established policies and procedures and aligned with the corporate goals
Perform bench work 20-30% of the time, for example sample receipt, order entry and specimen preparation, sample collection, and other lab activities as directed by Laboratory Manager
Follow and assess established Health and Safety procedures. Adhere and perform risk assessments. As well as understand, train, and enforce safety regulations
Maintain strong knowledge of HIPAA regulations
Meet at least monthly with direct reports. Provide coaching and constructive feedback, and career development discussions
Write and deliver quarterly/year end feedback and build a positive team environment
Provide evaluation of new process improvements and make appropriate recommendations based on through evaluation of operational, quality and efficiency impact
Coordinate staff training in partnership with dedicated trainers
Coordinate and/or monitor laboratory workflow to maintain accountability for staff productivity and other quality measures
Maintain operations by monitoring staff workload, adjusting schedules as needed, monitors, and maintains productivity standards and identifies opportunity for efficiency gain and quality improvements
Participate in the development, refinement and implementation of documents that affect the department
Establish, review, and implement training plans and checklists to ensure compliance to corporate policies and procedures
Troubleshoot sample, system and process issues raised by staff, customers, or others
Collaborate with IT, Engineers, and other cross-functional team to identify and resolve on-going process or system issues. Support corporate or customer-experience improvement projects by providing ideas, business requirements or end-user feedback as assigned, by supporting troubleshooting, end-user testing or task execution, as assigned
Collaborate closely within Lab Operations, Quality and Customer Service to improve process efficiency and ensure that each specimen is properly processed to sustain operations and maximize resource utilization
Represent the Accessioning department in cross-functional teams, as assigned
Participate and manage the interview, selection, hiring and on-boarding of new staff
Responsible for coaching, mentoring, disciplining, and training of department personnel, conducting 1:1’s and fostering an environment of open communication, partnering with staff to create and execute personal development plans
Provide timely feedback to staff, manage staff performance, write, and deliver annual staff performance reviews
Communicate goals clearly to employees to ensure understanding and success in achieving them
Motivate and inspire employees to do their best work through coaching
Maintain morale and support employee engagement initiatives
Communicate timely and regularly to management, stakeholders, and staff to ensure effective change management and address potential issues in advance
Participate in and/or assist with the preparation of internal and external audits and inspections
Review and maintain personnel files and department records in compliance with Quality Management System, applicable regulatory requirements such as CLIA, NY-CLIA, CAP, ISO standards and others
Strong communicator with ability to maintain open communication with internal employees, managers and customers as needed
Able to integrate and apply feedback in a professional manner
Able to prioritize and drive to results with a high emphasis on quality
Ability to work as part of a team
Recognized by others, internally and externally, for strong interpersonal skills, excellent written and verbal communication skills
Excellent listening, oral and written communication, and interpersonal skills
Ability to adapt to changes and identify ways to achieve goals
Self-directed, result oriented, able to operate independently
Ability and desire to thrive in a high-pressure, data-driven, and highly regulated work environment
Support and comply with the company’s Quality Management System policies and procedures
Regular and reliable attendance
Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for at least 50% of a typical working day
Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height
Ability to use a telephone through a headset
Ability to comply with any applicable personal protective equipment requirements
Standing or sitting for long periods of time may be necessary
Some lifting (greater than 25 pounds) may be necessary
May perform repetitious actions using lab tools
Ability to use near vision to view samples at close range
Use of various chemicals may be used to perform duties
Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork
Support and comply with the company’s Quality Management System policies and procedures
Maintain regular and reliable attendance
May be exposed to hazardous materials and tissue, blood, and other body fluid samples
Ability to comply with any applicable PPE requirements
Ability to act with an inclusion mindset and model these behaviors for the organization
Qualification
Required
High School Diploma or General Education Degree (GED), plus 4 years' experience working in a laboratory or similar environment (i.e., Medical Data Entry, maintaining sample integrity following procedures and protocols, etc)
OR Associates Degree in Science, health science, or related field, plus 3 years' experience working in a laboratory or similar environment (i.e., Medical Data Entry, maintaining sample integrity following procedures and protocols, etc)
OR Bachelor's Degree in Science, Health Science, or related field, plus 2 years' experience working in a laboratory or similar environment (i.e., Medical Data Entry, maintaining sample integrity following procedures and protocols, etc)
Previous supervisory experience or experience leading people or projects
Experience leading projects and/or project teams
Proficient with Microsoft Office Word, Excel, and Outlook
Demonstrated ability to perform the Essential Duties of the position with or without accommodation
Authorization to work in the United States without sponsorship
Preferred
Proven track or record of managing schedules
Professional working knowledge with using laboratory information management systems
Demonstrated ability to write and update procedures
Demonstrated knowledge of GDP, CAP, CLIA and NY
Experience in a high-volume clinical pathology laboratory operation
Demonstrate understanding of medical terminology, laboratory terminology and medical billing
Benefits
Paid time off (including days for vacation, holidays, volunteering, and personal time)
Paid leave for parents and caregivers
A retirement savings plan
Wellness support
Health benefits including medical, prescription drug, dental, and vision coverage
Company
Exact Sciences
Exact Sciences offers a portfolio of cancer screening and diagnostic tests that span from early detection to treatment monitoring.
Funding
Current Stage
Public CompanyTotal Funding
$2.75B2025-06-20Acquired
2024-04-11Post Ipo Debt· $620.7M
2023-02-23Post Ipo Debt· $500M
Recent News
2025-12-24
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2025-12-18
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