Biomat USA, Inc. Lead Medical Technologist in Memphis, Tennessee
For more than 75 years, Grifols has worked to improve the health and well-being of people around the world. We are a global healthcare company that produces essential plasma-derived medicines for patients and provides hospitals and healthcare professionals with the tools, information and services they need to deliver expert medical care.
This position is responsible for assisting the Laboratory Supervisor with the oversight of all laboratory operations, including all testing activities and personnel. This position will help organize and plan workflow, perform supervisory final result review and release, and assist with inventory control.
ESSENTIAL JOB FUNCTIONS:
- Assists with the oversight of laboratory operations and the personnel performing testing and reporting of test results.
Assists Laboratory Management with the monitoring of testing performed and the accurate and timely reporting of test results by laboratory personnel.
Assists Laboratory Management with the review and evaluation of all test records for completeness and compliance with all applicable procedural requirements, including customer-defined product test specifications.
Performs low, moderate, and high complexity testing of donor samples.
This position may perform supervisory final result review and release, as directed by Laboratory Management.
Ensures testing staff comply with IBBI written procedures for sample handling, processing, analyzing and reporting of test results.
Interfaces with vendor representatives and technical services to provide troubleshooting and diagnostic consultation to resolve instrument and assay technical problems.
Assists Laboratory Management in monitoring inventory control, reagent lot release, and process control indices.
Responsible for development, execution, and review of select validation protocols.
Coordinates and participates in the evaluation, validation, and implementation of new laboratory computer software and revisions and verifies that necessary validation documentation is maintained. Performs instrument, assay, and LIMS validations and training as directed by Laboratory Management.
Assists with the development of the training for laboratory employees.
Coordinates and may perform the training for the laboratory employees according to all required Standard Operating Procedures related to each job description and training requirements.
Routinely monitors and evaluates the effectiveness of the training and makes recommendations for additional and/or retraining as needed.
Develops Standard Operating Procedures, training procedures, training checklists, and other related documents and materials as required.
Performs quality control, calibration, and instrument maintenance activities as specified in procedures. Notifies supervision of any incidence of test results and/or test instruments not within the established acceptable levels of performance.
Notifies supervision of any problems identified that may adversely affect the performance of testing and/or the reporting of test results.
Initiates and assists with the completion of Error and Accident Reports associated with instrument, technical or assay performance incidents.
Performs supervisory duties, as authorized.
- Assumes the responsibilities of the Laboratory Manager in his/her absence. Performs other duties as may be required/assigned.
Interacts with Interstate centers and with Corporate personnel.
On-call availability when Organ/Tissue samples are processed.
QUALIFICATIONS / EXPERIENCE:
Must possess a current testing personnel license issued by the State in which the laboratory is located, if such licensing is required; and
Must be a doctor of medicine or doctor of osteopathy in the State in which the laboratory is located or have earned a doctoral, master's, or bachelor's degree in medical technology from an accredited institution
Must have previously qualified or could have qualified as a technologist under 42 CFR 493.1491 on or before February 28, 1992; or
Until September 1, 1997 - (1) must have eamed an academic high school diploma or equivalent; and (2) have documentation of training appropriate for the testing performed prior to analyzing patient specimens. Such training must ensure that the individual has been evaluated and found competent to perform the applicable tasks [Refer to 42 CFR 493.1489].
If the degree was not from an accredited institution in the United States, the individual must provide or the IBBI laboratory must obtain a documented statement saying that the degree eamed is equivalent to that required at accredited institutions in the United States.
Licensed as a general supervisor issued by the State in which the laboratory is located, if such licensing is required; and
Qualified as a Technical Supervisor of High Complexity Testing (CFR, Title 42, Part 493.1449); or
Qualified as a General Supervisor of High Complexity Testing (CFR, Title 42, Part 493.1461
Three years or more of laboratory experience.
Previous supervisory experience preferred.
Must have a working knowledge of State and Federal regulations regarding medical laboratory testing. Must have good interpersonal and communication skills
Must have above average problem-solving and decision-making abilities
Must be self-directed and highly-motivated
Must have excellent analytical skills, organization skills, and follow-up
Ability to effectively manage staff and maintain positive relationships with all levels of employees Experience in an FDA-regulated industry is preferred
Must have explicit attention to detail
- Must have ability to establish and maintain effective working relationships within The Interstate
Companies and provide excellent customer service
Ability to organize and prioritize work assignments
Ability to handle multiple priorities in a fast-paced environment
Ability to analyze situations and respond in a timely manner
Ability to participate in multi-functional teams and work in production areas Proficiency with computers
WORK ENVIRONMENT / PHYSICAL DEMANDS / TRAVEL:
Typical work environment with moderate noise level.
Ability to sit, stand, walk, stoop or crouch, hand/wrist use, talk, see, and hear for extended periods of time, examples include:
Stocks su lies, records in banker's boxes for retention
Stocks su plies, records in banker's boxes for retention
Stocks supplies, records in banker's boxes for retention
During routine job duties
During routine job duties
Documents information on forms, computer use
Looks for non-compliances and quality issues, records calibration
Listens for laborato activity, hears alarms, timi
Answers questions, presents information in small groups of customers, sup tiers or em 10 ees
Review of records
Keep task flow consistent, manage the amount of time needed for tasks, review records within the s ecified time frame
Concentrates on the task at hand, minimize distractions
SOPs, instructions, Job Aids, Forms, Package inserts, records, Company policies
Ability to work with toxic or caustic chemicals 20 - 30 % of the time.
Ability to read and understand documents, such as safety rufes, operating and maintenance instructions, procedure manuals, correspondence.
Ability to write short correspondence.
Ability to speak, answer questions, and or present information in small groups of customers, suppliers, or employees of the company.
Ability to add, subtract, multiply and divide. Ability to perform mathematical operations using units of US dollars, weight measurement, volume, and distance.
Ability to read a calendar, an analog clock, and use a calculator.
Ability to use a spreadsheet.
Ability to calculate sample suitability requirements.
Ability to apply common sense understanding to carry out detailed written or oral instructions.
Ability to deal with problems involving a few variables in routine situations.
Ability to lift up to 25 lbs.
Travel is negligible.
Daily attendance is required.
Learn more about Grifols
Req ID: 302927
Type: Regular Full-Time
Job Category: Nursing/Healthcare