Medical Laboratory Scientist

Full time 37.5 hours, Days

The Medical Laboratory Scientist II, in their role as Testing Personnel as defined by CLIA, may perform waived and non‑waived testing. Under general supervision, carries out all policies and performs all tests in accordance with the department's standard operating procedures. Works independently in an efficient and organized manner to assure accurate results and records. The work requires a professional level of knowledge to read and interpret accurately test results used by providers in the diagnosis and treatment of diseases.

The Medical Laboratory Scientist II, in their role as General Supervisor as defined by CLIA, may be delegated the responsibility of the day‑to‑day supervision or oversight of the laboratory operations and personnel performing testing and reporting results. Under the general supervision of the Laboratory Manager and Clinical Supervisors, the Medical Laboratory Scientist II is responsible for supervision of assigned workstations including Quality Control (QC) review, training, competency assessment of staff and inventory management.

The testing personnel are responsible for specimen processing, test performance and for reporting test results. Each individual performs only those tests that are authorized by the laboratory director and require a degree of skill commensurate with the individual's education, training or experience, and technical abilities.

Bachelor's Degree in Medical Technology or Bachelor's Degree in Laboratory Sciences required;
Other certificate/diploma in Clinical Laboratory Sciences also required.

Medical Technologist (ASCP) – American Society for Clinical Pathology Board of Certification (ASCP‑BOC) preferred.

Lab experience 1‑2 years required.

• Proficient in laboratory equipment operation, maintenance, repair, and analytical techniques.
• Demonstrated ability to work independently, assess situations, and respond appropriately.
• Skilled at multitasking in a fast‑paced environment while maintaining accuracy.
• Strong attention to detail and adherence to SOPs and regulatory protocols.
• Proactive in identifying and communicating issues to supervisors.
• Effective team player with strong interpersonal and communication skills.
• Ability to interact professionally with a wide range of personnel including physicians, hospital staff, and patients.
• Working knowledge of CLIA, CAP, and other applicable federal, state, and accreditation requirements.
• Willingness to assist with inventory control, implementation of new QC materials, and participation in method validations and instrument verification as needed.

This position will be working in the Microbiology and/or Chemistry lab with rotating weekends and holidays.

Cooley Dickinson Hospital, Inc. is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.