Grifols Veterans Jobs

GFL700 <br></p><p><img src="http://www.grifols.com/documents/239901/1137346/SuccesFactors_1020x93_jobposting_line_test.png/ec7da48f-8161-41cb-b53a-7a36f6a376a6" width="100%"></p><p></p><p></p><p><a href="http://www.grifols.com/es/web/international/home" target="_blank">Learn more about Grifols</a></p><p></p><br><strong>Req ID:</strong> 303008 <br><strong>
able.MiTabla { max-width: 1020px;!important </p><img align="top/" alt="" src="https://www.grifols.com/documents/239901/1024085001/SSFF_01_BSC.jpg/94a9db8b-2c43-45fd-994e-0896e715aac7"><p style="text-align:justify">Do you want to join an international team wor
vices in more than 100 countries and regions. </p><img src="http://www.grifols.com/documents/239901/1137346/SuccesFactors_1020x93_jobposting_line_test.png/ec7da48f-8161-41cb-b53a-7a36f6a376a6"><p>SUMMARY: <br> This position is responsible for as

Job Information

Interstate Blood Bank Serology Laboratory Lead Technologist in Memphis, Tennessee

Do you want to join an international team working to improve the future of healthcare? Do you want to improve the lives of millions of people? Grifols is a global healthcare company which, since its foundation in Barcelona in 1909, has been working to improve the health and well-being of people all over the world. Our four divisions - Bioscience, Diagnostic, Hospital and Bio Supplies - develop, produce and market innovative medicines, solutions and services in more than 100 countries and regions.

SUMMARY:

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:

Daily:

  • 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.

Frequent:

  • Assumes the responsibilities of the Laboratory Manager in his/her absence.

  • Performs other duties as may be required/assigned.

Infrequent:

  • 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

  • ;

or

  • 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 earned 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

  • 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 earned 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:

Activity Typical Duties

Reaching Stocks supplies, records in banker’s boxes for retention

Climbing Stocks supplies, records in banker’s boxes for retention

Bending/Stooping/Lifting Stocks supplies, records in banker’s boxes for retention

Standing During routine job duties

Walking During routine job duties

Hand/Wrist Use Documents information on forms, computer use

Observing/Seeing color Looks for non-compliances and quality issues, records calibration

Hearing/Listening Listens for laboratory activity, hears alarms, timing devices

Talking/Communication Answers questions, presents information in small groups of customers,

suppliers or employees

Sitting Review of records

Time Management Keep task flow consistent, manage the amount of time needed for tasks,

review records within the specified time frame

Focusing Concentrates on the task at hand, minimize distractions

Reading 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 rules, 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.

Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities

to this job at any time.

EEO Minorities/Females/Disability/Veterans

#IBBI

CLK 789

GFL700

Learn more about Grifols

Req ID: 303008

Type: Regular Full-Time

Job Category: Nursing/Healthcare

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