In Vitro Sample Analysis

Connecticut Behavioral Health Associates, P.C.
Groton, CT, United States
3 months ago

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Job source

Tech stack

Computer Literacy GXP

Job description

Testing personnel are responsible for the performance of patient clinical testing to include some specimen processing, with quality control and test performance. This will include pre-analytical, analytical and post-analytical duties as described in the following section for this facility. Established protocols and procedures of this facility must be followed to ensure quality patient care., * Follow laboratory’s procedures for specimen handling and processing, test analysis, reporting and maintaining records of patient results.

  • Adhere to laboratory policies for:

  • Instrument Maintenance

  • Instrument and procedural calibration

  • Quality Control (QC) performance

  • Documentation of maintenance, calibration and QC activities

· Identify problems that may adversely affect test performance or reporting of test results and either correct the problem or notify the appropriate supervisor.

· Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications.

  • Ensure the confidentiality of all patient information throughout all phases of laboratory testing. The privacy of each patient must be maintained by preventing all confidential information from being seen or heard by unauthorized persons, including other patients, visitors to the facility and any unauthorized party outside this facility.
  • Ensure the procedure manual is complete and updated when necessary when changes are made to testing procedures, instruments, methods, etc. Any changes must be adopted by the Laboratory Director.
  • Perform and document all routine daily, weekly, monthly, and periodic maintenance and function checks following established protocol. Document all maintenance performed on instrument log sheets.
  • Formulate stock solutions for reagents, internal standards and Quality control material according SOP guidelines and established protocol.
  • Demonstrate knowledge, understanding and proficiency in the preparation, processing and analysis of biological samples using LCMS testing.

Requirements

Do you have experience in Computer literacy?, Do you have a Bachelor’s degree?, * Knowledge of good laboratory practices and other regulatory agency standards within area of responsibility.

  • Knowledge of laboratory equipment, instrumentation and terminology used in the area of responsibility.
  • Basic computer skills
  • Ability to maintain effective reporting procedures and control workflow.
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients

Post-Analytic:

  • Review and release patient results for screening and confirmation testing.
  • Retain records of all patient reports, errors, notifications, and corrective actions for a minimum of two years and make available for inspection., * Bachelor’s degree or Master’s degree in a chemical, physical, biological, or clinical laboratory science

Physical Requirements

Typical functions of this role include standing, sitting and walking a majority of the time. There are occasions when kneeling, stooping, bending or reaching may be necessary.

The employee must be able to lift and/or move up to 10 lbs on a regular basis.

The noise level in the work environment is usually mild to moderate. Exposure to fumes, airborne particles and chemicals and risk of electric shock can occur.

Job Type: Full-time

Required experience:

  • BioLis 24i / LCMS/MS is a plus

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