Medical Technologist II - Monday-Friday 8a-5p
About the role
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Each individual performing high complexity testing must
1) Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results;
2) Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens;
3) Adhere to the laboratory's quality control policies,
4) Document all quality control activities, including instrument and procedural calibrations and maintenance performed;
5) Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance;
6) Be capable of identifying problems that may adversely affect test performance or reporting of test results;
7) Demonstrate knowledge and capacity to either correct the recognized problems or immediately notify the general supervisor, technical supervisor, clinical consultant, or director;
8) Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications
Required Experience
Applicant should have at least 4 years of experience in a Clinical Molecular Laboratory that includes:
- Nucleic acid extraction from blood, bone marrow aspirate, FFPE tissue, plasma
- Utilization of Next Generation Sequencing (NGS) and PCR-based clinical assay methods and platforms
Applicant should have strong knowledge, skill, and/or abilities in:
- Good documentation practices
- College of American Pathologist (CAP) requirements and guidelines
- Excellent written, verbal, and interpersonal communication skills
- Proficient use of computers/scanners/copiers/printers, including Word and Excel applications
- Demonstrated knowledge of operational characteristics of apparatus, equipment, and materials used in a regulated clinical laboratory
- Sterilization and decontamination techniques, including hazardous waste disposal
- Commitment to participate as a constructive, contributing team member of a dynamic, clinical diagnostic work group
- Commitment to compliance with all MolecularMD/ICON safety and regulatory work practice guidelines and procedures as defined in the Quality Management Program, the Chemical Hygiene Plan, confidentiality and HIPAA agreements, and all applicable state and federal regulations and requirements
Education and Work Experience
- BA/BS in Biology, Molecular Biology, Medical Technology or Molecular Biology, or related science and 4 years of experience in a Clinical Molecular Laboratory
- or Master's Degree in Biology, Molecular Biology, or related science and 2 years of experience in a Clinical Molecular Laboratory
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