Clinical Laboratory Supervisor

The Molecular Technologist supervisor shall perform routine molecular and chemistry laboratory procedures and techniques used for the preparation, processing, and analysis of nucleic acid and blood samples. All high-complexity testing and tasks shall be performed in accordance with established departmental and quality control procedures and laboratory approved protocols.

Essential Responsibilities:

• Performs high-complexity tests as authorized by the technical supervisors.
• Prepare human samples for analysis using genomic nucleic acid preparation techniques.
• Perform PCR (polymerase chain reaction), reverse transcription PCR, and Real time PCR techniques on nucleic acid samples.
• Perform Sequencing Techniques (eg. Sanger sequencing, NGS, OpenArray, etc.).
• Analyze results and data produced from the nucleic acid procedures (as above).
• Be proficient in using various software analysis programs and databases.
• Be proficient in computer software platforms .
• Develop, draft, and assist in creating and updating protocols.
• Maintain complete and accurate documentation and records.
• Perform quality control and quality assurance documentation in accordance with lab protocols and regulations.
• Test newly developed lab procedures and techniques, as directed and report on results.
• Perform case review prior to final report.
• Train other staff as assigned.
• Perform other related duties as qualified, trained and assigned.
• Position requires interaction with the receiving laboratory staff on a regular basis regarding specimens, cultures and other related matters.
• Position requires to accession specimens into LIS system.
• Laboratory tests, techniques and procedures will require periodic change. Therefore duties and responsibilities will be subject to change.
• Prepares reports, maintains records, administrative information, Prepares and presents work-related information to supervisor.
• Researches qualitative and quantitative methods in the appropriate laboratory specialty area. Performs statistical analysis on quality control and quality assurance monitors.
• Performs all assigned duties in a timely and efficient manner.
• Coordinates quality control activities with the supervisor. Coordinates proficiency program for the appropriate laboratory specialty.
• The technologist independently plans and carries out the procedures necessary to complete the work assignment and handles problems and corrects errors in accordance with established protocols or accepted laboratory practices.
• Determine acceptability of specimens and/or blood or blood components, perform laboratory tests and communicate critical results in accordance with laboratory policy for assigned section or shift and/or obtain and record results for laboratory tests according to established procedures within established TAT as delegated by the Chief of Pathology.
• Recognizes normal, abnormal, critical test results. Differentiates and resolves instrument and/or unexpected test results
• Understand and adhere to Lean principles and processes , for example, following standard work and maintaining 5S concept in work area realizing that all processes are driven by the needs of the customer.
• Initiate, perform, review and troubleshoot quality control of reagents and test systems.
• Maintain all clinical competencies required in section and perform in accordance with laboratory policy to provide accurate test results, slides, photographs and/or documents.
• Operate and perform daily preventive maintenance of equipment according to written procedures and documents; report equipment malfunctions and request service as necessary.
• Communicate with physicians, nurses, or other requestors by telephone, computer or other method that ensure confidentiality.
• Actively participate in inventory control and supply chain operations through application of Lean principles.
• Look for, initiate and/or participate in quality improvement opportunities. Actively look for ways to improve standard work processes and share insights to that end with team member, team leaders, and group leaders with the same level of importance as performing quality technical work.
• Promote teamwork and cooperation through helpful, courteous, and positive interactions with colleagues
• Promote a trusting and secure work environment .through supportive, dependable interactions
• Take ownership of performance and PEAC process by understanding lab goals and objectives and aligning individual activities and performance with hospital and lab goals and objectives.
• Using an awareness of how the work performed is valued by the customer, perform duties, make decisions, take actions and continually strive to improve work processes.
• Maintain inspection readiness. Demonstrate knowledge and ownership of current inspection requirements for all applicable regulatory and accrediting agencies relating to area of responsibility. Participate in tracers, mock inspections, regulatory reviews and Quality Assurance meetings as required.
• Attend and participate in shift stand up meetings, staff meetings and Laboratory Town Hall meetings.
• Share knowledge and provide instructions to new employees, students, other technologists, technicians and other staff.
• Pursue continuing education.
• Perform other duties and special projects as requested.
• Read and adhere to all laboratory policies and procedures pertaining to section and document understanding of such.

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Basic Qualifications:

Experience

• Minimum two (2) years of experience in a clinical or research molecular biology and chemistry laboratory performing clinical molecular and chemistry diagnostic testing procedures and techniques
• Education: Bachelor's Degree in biological or Clinical Laboratory science or a field related to genetics from an US-accredited college or university or equivalent.
• License, Certification, Registration: Technologist in Molecular Biology by the ASCP (American Society for Clinical Pathology or equivalent certifying body approved by the state) preferred.

Additional Requirements:

• Must have the demonstrated ability to perform clinical molecular diagnostic testing procedures and techniques as defined by the Employer.
• Must be able to analyze results and data produced from the testing and perform case review prior to final report.
• Ability to read and comprehend protocols, instructions, correspondence, and memos, and to communicate as the job requires.

Job Type: Full-time

Pay: $28.00 - $40.00 per hour

Expected hours: 40 per week

Benefits:

• Flexible schedule
• Paid time off

Schedule:

• 8 hour shift
• Evening shift
• Monday to Friday
• Weekends as needed

Application Question(s):

• How many years of clinical molecular biology experience do you have?

Experience:

• Blood, QC and calibration: 1 year (Preferred)
• Clinical chemistry: 1 year (Preferred)
• AU680 Clinical Chemistry Analyzer: 1 year (Preferred)
• DxI 800 Access Immunoassay System: 1 year (Preferred)
• Sysmex hematology analyzer: 1 year (Preferred)

Work Location: In person