Description:

Supervises the overall operation of the laboratory including coordinating, planning, organizing, and evaluating the laboratory services provided for clients. Responsible for the quality programs and adhere to all regulatory standards. Directs and supports lab personnel including training and development. The supervisor must always be accessible when personnel testing is performed to provide consultation and to resolve technical problems in accordance to written policies and procedures established by the laboratory director. In addition, the supervisor is responsible for monitoring test analyses and specimen examinations to ensure that acceptable levels of analytic performance are maintained. The supervisor is responsible for the proper performance of all laboratory procedures and reporting of test results. Clinical laboratory supervisor responsibilities are in accordance with CLIA regulations, Subpart M- Personnel and Part 493- Laboratory Requirements may apply. In addition, adherence to all accreditation policies and guidelines pertaining to the laboratory. Education and Experience • Meet all the qualifications for high complexity testing by CLIA/COLA regulations • Supervisor Experience • Bachelor's degree in a relevant scientific discipline (e.g., Chemistry, Biochemistry, Analytical Chemistry) or B.S. (or higher) in Biology, Medical Technology, or related field • Proven experience in operating and maintaining LCMS equipment • Strong analytical and problem-solving skills • Attention to detail and accuracy in data interpretation • Excellent communication and collaboration skills • Knowledge of relevant laboratory safety and regulatory guidelines • Experience with method development and optimization • Familiarity with software for data analysis and instrument control • Ability to work independently and in a team environment • Strong organizational and time-management skills • Supervise all testing performance, corrective actions, and process improvement • Maintain QA/QC records and programs • Maintain strict CLIA/COLA Compliance • Collaborate with internal teams, vendors, and others as needed to resolve issues, maintain ongoing functionality, and document service, project management and repair work • Supervise laboratory personnel by preparing schedules, providing guidance and direction • Oversee laboratory and accessioning personnel performance, training, and competency • Perform or delegate instrument validation, maintenance, and troubleshooting • Prior supervisory experience is required • They need to be familiar with LC/MS, and if it is Schimadzu it is a plus

Skills:

pcr, Laboratory, Medical laboratory, Molecular, Chemistry, Biology, Mlt, Microbiology, Toxicology, Clinical laboratory

Top Skills Details:

pcr,Laboratory,Medical laboratory,Molecular,Chemistry,Biology,Mlt,Microbiology,Toxicology,Clinical laboratory

Additional Skills & Qualifications:

• Performs the duties of a technologist in the specialty or specialties as needed. However, the supervisor remains responsible for ensuring that direct supervision is properly performed. The assignment of responsibilities from the supervisor to the technologist must be written and specific. • Evaluates the competency of technologists and technicians and assures that the staff maintain their competency to perform test procedures and report test results promptly, accurately, and proficiently. Refer to guidelines from CLIA/COLA for evaluation. • Available to clinical laboratory personnel at all times testing is performed and provides on-site telephone or electronic consultation to resolve technical problems according to Labworks policies and procedures approved by the laboratory director. • Assures that all remedial actions are taken whenever test systems deviate from the clinical laboratory’s established performance specifications. • Adheres to perform all Proficiency Test samples in the same exact procedure as patient’s samples and confirm all results are uploaded correctly into the COLA website after reviewed with Technical Supervisor and Lab Director. • Follows guidelines that patient test results are not reported until all corrective actions have been taken and the test system is properly functioning. • Prepares and help the Technical Supervisor with updates policy and procedure manuals. • Maintains laboratory’s quality controls, control policies, instrument, and calibration procedures all under the guidelines and regulations in the SOP. • Refers to the clinical laboratories policies and procedures when test systems are not within the laboratory’s defined acceptable levels of performance.

Experience Level:

Expert Level

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent

• Maintaining an inclusive environment through persistent self-reflection

• Building a culture of care, engagement, and recognition with clear outcomes

• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.