Join the Clinical Laboratory team of an emerging diagnostic leader offering proprietary biomarker testing for neurodegenerative diseases. Responsible for pre-analytical, analytical, and post-analytical processes associated with specimen processing, test performance and test result reporting.
Duties and Responsibilities:
- Follow the laboratory’s procedures for specimen handling, labeling, processing, transportation, and storage.
- Responsible for monitoring test performance and specimen examinations to ensure that acceptable levels of analytic performance are maintained.
- Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and maintenance performed.
- Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance.
- Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications.
- Open shipping packages containing human medical specimens.
- Preparation, testing/qualification, and storage of reagents.
- Accurate transcription of handwritten and printed documentation onto worksheets and into laboratory information systems.
- Review, develop and/or author SOP’s and other regulatory documentation.
- Assist in the training of new personnel.
- Assist in the development of new clinical tests.
- May transmit patient results to clients.
- May participate in the performance review process for others.
- Attend and participate in intra and interdepartmental meetings, as required.
- General Supervisor duties will be established per Laboratory Directory delegation form, as applicable.
- Function as laboratory point person for incoming R/D or pharma projects.
- Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens.
- Ensuring that patient test results are not reported until all corrective actions have been taken and the test system is properly functioning.
- Perform all duties in keeping with the company’s core values, policies, and all applicable regulations.
- Other duties may be assigned.
Job Related Experience and Qualifications:
Required (minimum):
- Minimum of two (2) years of laboratory experience in high complexity testing; excellent communication/interpersonal skills/problem-solving; highly organized and detail oriented; self-directed and accountable.
Preferred:
- Experience with molecular testing; experience with assay development and validation processes; qualifies as General Supervisor.
Job Type: Full-time
Pay: $42.00 - $53.00 per hour
Benefits:
- 401(k)
- Dental insurance
- Flexible schedule
- Health insurance
- Paid sick time
- Paid time off
- Vision insurance
Schedule:
- 8 hour shift
- Monday to Friday
Shift availability:
Work Location: In person