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Mastech Digital

Clinical Laboratory Scientist

Mastech Digital, San Diego, California, United States, 92189

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Overview

The

Clinical Laboratory Scientist I (CLS I)

will perform

analytical testing

as well as

general laboratory processes

in a

high complexity clinical molecular laboratory

in compliance with policies, procedures and regulations. Responsibilities

Performs

clinical testing of patient samples , including set-up of

molecular assays . Adheres to the laboratory’s

quality control processes

and documents

quality control activities ,

instrument and equipment verifications , and

instrument maintenance and preventive maintenance . Supports the

Corporate and Laboratory Operations Goals and Objectives . Follows the laboratory’s

policies and procedures

when test systems are not within established performance specifications. Identifies and documents

problems that may adversely affect test performance

and notifies the manager or director. Documents all

corrective actions

taken when test systems deviate from established specifications. Participates in activities required to support all necessary

licensure for the clinical laboratory , including maintaining

quality systems

and

test records

and supporting on-site inspections of the laboratory. Utilizes an

in-house Lab Information System (LIS) . Complies with all

local, state, and federal laws and regulations

governing clinical laboratory operations. Maintains records demonstrating that

proficiency testing samples

are tested in the same manner as patient specimens. May be required to

monitor the activities of non-licensed personnel . May be required to

assist in assay development activities . Performs other duties as assigned. Minimum Education/Experience Requirements

Clinical Genetics Molecular Biologist (CGMBS)

or

Generalist Clinical Laboratory Scientist (CLS) License

from the State of California Bachelor’s Degree in Medical Technology or Biological Sciences . Must meet the requirements for

Testing Personnel under CLIA 88 (42 CFR, part 493) Highly organized , able to

work independently , follow

standard operating procedures . Experience in a

high complexity CLIA/CAP environment

strongly preferred Experience in

Molecular Biology ,

Molecular Pathology , and/or

Medical Genetics

preferred Required Training/Certification

On the job training including, but not limited to:

HIPAA , and

safety procedures . Seniority level

Mid-Senior level Employment type

Contract Job function

Other Industries

Medical Equipment Manufacturing

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