
Supervisor, Pre-Analytical Laboratory
Abbott Laboratories
Summary
The Supervisor, Pre-Analytical Laboratory is responsible for supervision of team members and daily operations of the Pre-Analytical (Accessioning) department including specimen box receipt process, test order processing, sample processing, material return and management of associated documents and records. They serve as a liaison between Accessioning and various functional groups to report and address immediate issues or concerns. They are also responsible for coordinating or leading the laboratory workflow and scheduling, troubleshooting high complexity technical and non-technical problems, building an effective team, managing projects and deliverables.
Job description
Position Overview
The Supervisor, Pre-Analytical Laboratory is responsible for supervision of team members and daily operations of the Pre-Analytical (Accessioning) department including specimen box receipt process, test order processing, sample processing, material return and management of associated documents and records. They serve as a liaison between Accessioning and various functional groups to report and address immediate issues or concerns. They are also responsible for coordinating or leading the laboratory workflow and scheduling, troubleshooting high complexity technical and non-technical problems, building an effective team, managing projects and deliverables.
Essential Duties
- 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. 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 thorough 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 teams to identify and resolve on-going process or system issues.
- 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 onboarding of new staff.
- Responsible for coaching, mentoring, disciplining, and training of department personnel, conducting 1:1's and fostering an environment of open communication.
- 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.
Minimum Qualifications
- High School Diploma or General Education Degree (GED), plus 4 years' experience working in a laboratory or similar environment.
- Or Associates Degree in Science, health science, or related field, plus 3 years' experience working in a laboratory or similar environment.
- Or Bachelor's Degree in Science, Health Science, or related field, plus 2 years' experience working in a laboratory or similar environment.
- 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 Qualifications
- 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.
Requirements
- High School Diploma or GED plus 4 years' laboratory or similar environment experience, OR Associate's Degree in Science/Health Science plus 3 years' experience, OR Bachelor's Degree in Science/Health Science plus 2 years' experience
- Previous supervisory experience or experience leading people or projects
- Experience leading projects and/or project teams
- Proficient with Microsoft Office Word, Excel, and Outlook
- Authorization to work in the United States without sponsorship
Benefits
- Medical coverage
- Retirement savings plan
- Tuition reimbursement
- Student debt program
- Education benefit
- Career development
Company overview
Abbott Laboratories is a global healthcare technology leader founded in 1888 and headquartered in Chicago, Illinois. As an international medtech and pharmaceutical company, Abbott operates in approximately 160 countries worldwide with a workforce of over 115,000 employees. The company is organized into four major business segments: Medical Devices (48% of revenue), Diagnostics (20%), Nutritional Products (19%), and Established Pharmaceutical Products (12%). Abbott's medical devices portfolio includes revolutionary technologies such as the FreeStyle Libre continuous glucose monitoring system for diabetes management, cardiovascular devices like the MitraClip and TriClip for heart valve repair, and neuromodulation systems for chronic pain management. The company's diagnostics division pioneered breakthrough tests including the first licensed HIV blood test in 1985. With a rich history spanning over 135 years, Abbott has consistently been recognized as one of Fortune's World's Most Admired Companies since 1984 and continues to drive innovation in healthcare technology to help people live healthier, fuller lives.