Supervisor- In- Operations

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients.

With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.

Location:

Madison, WI!

Work Schedule:

Monday-Friday 6:30 am-3:30 pm CST some weekends required.

• As a supervisor you will supervise and coordinates the efforts of a team of operational staff for nonclinical regulatory and non-regulatory studies in drug development.
• Contributes to the hiring, coaching, scheduling/delegating work, conducting performance reviews, and determining pay/promotions.
• Ensures testing is completed by established deadlines in compliance with SOPs, GLPs, and regulatory agency guidelines.
• Monitor’s animal health and welfare in compliance with the Animal Welfare Act and help maintain facilities for AAALAC compliance.
• Schedules and coordinates proactively and in conjunction with other groups or departments the daily activities of the group and liaises with other groups, sections and departments.
• Organizes necessary resources for conducting all relevant study or non-study related tasks and participates in the study performance.
• Assures appropriate communication within the group, particularly for dissemination of information (i.e. Study progress, Facility procedures, Quality, Health and Safety, Business Updates and any other departmental or company communications).
• Understands and interprets study plans and identifies problems resulting from the study plan or during study conduct and takes appropriate action.
• Optimizes existing and develops new techniques, methods for study conduct or non-study specific areas and supports their application.
• Plans, organizes and participates in meetings (i.e. study start-up meetings, coordination meetings).
• Performs quality controls, assures corrections of errors (incl. documentation) identifies potential problems and optimizes the quality control system.
• Ensures maintenance of instruments and equipment is performed (i.e. maintenance, validation and calibration), ensures that non-performing equipment is removed and may maintain inventory lists and ensures replacement or new purchase on time.
• Responsible for constructive responses to reports and questions from Study Direction, QAU, EH&S, clients or regulatory agencies in a timely manner.
• Performs corrective actions when needed.
• Provides for safety and welfare of staff and supports/enforces Environmental Health and Safety Policies.
• May be asked to participate in global working groups.
• Takes responsibility for certain areas (e.g. Necropsy or Histology laboratory, equipment, methods, inventory of supplies, disposal, etc.).
• Reports all animal welfare concerns and becomes involved in the resolution and appropriate corrective action, when necessary.
• Provides support, training and guidance for less experienced staff.
• Learn our cost structure and how to proactively impact it.
• Participates in meetings, inspections or client visits.
• Performs other duties as assigned.

• Bachelor’s degree in a Life Science…