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Posted: 13-Nov-24
Location: Indianapolis, Indiana
Type: Full-time
Salary: Open
Categories:
Internal Number: 2443714
***Sign-on Bonus $7,500 (For External Candidates)***
Labcorp Drug Development, the world?s most comprehensive drug development company, dedicated to improving healthcare and improving lives. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, along with our innovative technology solutions, help our clients identify new approaches and anticipate tomorrow?s challenges as they evolve.
We have an exciting opportunity for a Medical Technologist II to join our Safety team in Indianapolis, IN!
Scheduled Shift: Monday-Friday 3pm-11:30pm, rotating Tuesday-Saturday 3pm-11:30pm
Benefits: All job offers will be based on a candidate?s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Commissions, and Company bonus where applicable. For more detailed information, please click here.
Incumbent performs established procedures for clinical testing as required in all assigned laboratory disciplines. Incumbent is responsible for analyzing specimens whose results are then reported to the sponsor. Incumbent proactively seeks out opportunities to improve processes and procedures and demonstrates initiative in resolving problems. Supports quality control/quality assurance monitoring programs, and is responsible for assisting with training of personnel.
Essential Job Duties:
Perform duties of Technologist I, and may perform duties of Technologist II in addition to the following additional duties:
Essential Functions
¨ Quality Control Monitoring Programs
o Review and investigate unacceptable results to internal and external quality control monitoring programs. Prepare corrective action responses by assigned due date for management review.
¨ SOPs
o Complete timely review of new or revised SOPs circulated for peer review.
o May assist with timely processing of SOPs for department.
¨ Proficiency Testing Survey Samples
o May provide support to proficiency testing program by coordinating receipt of survey material, coordinating with interdepartmental personnel for sample analysis, and ensuring timely and correct completion of electronic or paper report forms.
o Investigate root cause for unacceptable performance on proficiency surveys and prepare corrective action response by assigned due date.
¨ Training
o Assists with training new employees and follows-up to ensure training is understood.
o May assist with the development of training material, training checklists, and competency assessment programs.
¨ Instrument/Equipment/Assay Validation
o Assist with assay validations by performing experiments according to departmental SOP. Compile validation data for management review.
o Assist with validation of new equipment and instruments including software validation requirements (e.g., User Acceptance Testing).
¨ Assist staff by providing technical guidance where needed.
Non-Essential Functions
¨ Only individuals that are verified to qualify as supervisory personnel under regulations/standards applicable to the facility (e.g., New York State, CLIA, CAP) may perform periodic review and approval of quality control program records (e.g. quality control
data, instrument logs, reagent logs). The SOPs applicable to the department should be consulted to determine records that can be reviewed and approved.
Minimum Experience Required:
Individual should have >5 years external clinical laboratory testing experience or 1 year of Covance Laboratory experience performing clinical laboratory testing.
Education/Qualifications/Certifications and Licenses
U. S. Requirements
Individual must qualify as testing personnel under the following CLIA 1988 and New York State Department of Health requirements:
· Bachelor?s degree in Medical Technology or Clinical Laboratory Science or other life science with completion of at least a 12-month training program in Medical Technology.
OR
· Bachelor?s degree in a chemical, physical or biological science from an accredited college or university and one year training and/or experience in the specialty in which testing is to be performed. Such training must be equivalent to that received in a school of Medical Technology.
OR
· 90 semester hours from an accredited institution that include the following:
1) 16 semester hours of biology courses, which are pertinent to the medical sciences
2) 16 semester hours of chemistry (at least 6 semester hours of Inorganic Chemistry)
3) 3 semester hours of math
· Completed an accredited clinical laboratory training program, or one year documented laboratory training or experience in the specialty that testing is to be performed.
OR
· Associate?s degree in medical laboratory technology
Preferred Experience
- Two or more years clinical laboratory testing experience
- Automation experience and automated chemistry experience
- Serum Chemistry experience
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.
We encourage all to apply
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