Quest Diagnostics Employer Solutions
Medical Laboratory Scientist II - RRL Float
Quest Diagnostics Employer Solutions, Saint Paul, Minnesota, United States, 55130
Overview
Medical Laboratory Scientist II - RRL Float (#25859) at Quest Diagnostics Employer Solutions. This role is listed as part of Quest Diagnostics Employer Solutions. Benefits
We are proud to offer best-in-class benefits and programs to support employees and their families in living healthy, happy lives. Depending on part-time or full-time status, some benefits may include: Day 1 Medical/Dental/Vision for FT employees who work 30+ hours. 15 PTO days first year. Paid Holidays. 401(k) with matching contributions. Employee Stock Purchase Plan (ESPP). Employee Assistance Program (EAP). Blueprint for Wellness. Tuition Reimbursement for undergraduate and graduate programs for FT employees who work 30+ hours. Opportunities for career advancement. Training provided. Annual Bonus Opportunity (listed in some variants). Variable compensation plan (AIP) bonus (listed in some variants). Responsibilities
Perform and report on assigned analytical tests under the direction of senior personnel in accordance with applicable Standard Operating Procedures (SOP) ensuring that applicable quality control requirements are met. May perform some moderate complexity testing with specific on-site training and oversight. Actively support and comply with laboratory policies and procedures for specimen handling and processing, test analysis, reporting, and maintaining records of patient test results. Adhere to analytical schedules to maintain a turnaround time of results including STATS or critical results to clients. Ensure reagents/test kits have received dates, expiration dates, and if applicable opened dates. Perform and document QC analysis to ensure the accuracy of clinical data and proper instrument function. Make quality control decisions regarding the disposition of an assay or test. Responsible for informing supervisory personnel of all problems associated with the proper performance of test procedures. Report any actual or potential deviation from standard or accepted testing procedures and cooperate fully with any investigation of same. Review and enter test results into the Laboratory Information System for standardized reports to be generated for physician review and interpretation. Maintain laboratory areas and equipment in a safe, functional, and sanitary condition. Complete training and competency checklists as appropriate. Adheres to all established CLIA, HIPAA, OSHA, and laboratory safety requirements. Required to use (a) personal protective equipment, (b) engineering controls, and/or (c) work practice controls as directed by management. Answer questions from clients or other lab personnel, if applicable. Participate in government or regulatory agency inspections, if needed. Other duties as assigned. This is not an exhaustive list of all duties and responsibilities, but rather a general description of work performed by the position. Qualifications
Required Work Experience: Previously qualified as a Technologist under 42 CFR 493.1433 published in March 14, 1990. Preferred Work Experience: One (1) to three (3) years of clinical experience preferred. Physical And Mental Requirements
The normal performance of duties may require lifting and carrying objects: 1 to 10 pounds frequently; 11 to 25 pounds occasionally; 36 to 50 pounds seldom; over 50 pounds not to be lifted without assistance. Ability to stand and work at the bench for long periods of time. Frequent walking and/or standing. May be required to use a wide variety of manual and automated pipettes and laboratory instruments and apparatuses, all demanding significant manual dexterity. Knowledge
Basic theoretical and operational knowledge in clinical testing. Knowledge of organizational/departmental policies and procedures. Skills
Detail-oriented, able to work independently, establish priorities, and handle several tasks simultaneously. Interpersonal skills to work with supervisors, co-workers, and clients. Communication skills to handle telephone inquiries from clients. Ability to handle client information confidentially. Proficiency in Microsoft Office (Word, Excel, Outlook) and Laboratory Information Systems. Education
Associates Degree (Required). Bachelors Degree. LICENSE CERTIFICATIONS:
ASCP Certification. For a full list of Quest Diagnostics careers, please visit: Quest Diagnostics Careers All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. Quest Diagnostics is an Equal Opportunity Employer: Women / Minorities / Veterans / Disabled / Sexual Orientation / Gender Identity / Citizenship. #J-18808-Ljbffr
Medical Laboratory Scientist II - RRL Float (#25859) at Quest Diagnostics Employer Solutions. This role is listed as part of Quest Diagnostics Employer Solutions. Benefits
We are proud to offer best-in-class benefits and programs to support employees and their families in living healthy, happy lives. Depending on part-time or full-time status, some benefits may include: Day 1 Medical/Dental/Vision for FT employees who work 30+ hours. 15 PTO days first year. Paid Holidays. 401(k) with matching contributions. Employee Stock Purchase Plan (ESPP). Employee Assistance Program (EAP). Blueprint for Wellness. Tuition Reimbursement for undergraduate and graduate programs for FT employees who work 30+ hours. Opportunities for career advancement. Training provided. Annual Bonus Opportunity (listed in some variants). Variable compensation plan (AIP) bonus (listed in some variants). Responsibilities
Perform and report on assigned analytical tests under the direction of senior personnel in accordance with applicable Standard Operating Procedures (SOP) ensuring that applicable quality control requirements are met. May perform some moderate complexity testing with specific on-site training and oversight. Actively support and comply with laboratory policies and procedures for specimen handling and processing, test analysis, reporting, and maintaining records of patient test results. Adhere to analytical schedules to maintain a turnaround time of results including STATS or critical results to clients. Ensure reagents/test kits have received dates, expiration dates, and if applicable opened dates. Perform and document QC analysis to ensure the accuracy of clinical data and proper instrument function. Make quality control decisions regarding the disposition of an assay or test. Responsible for informing supervisory personnel of all problems associated with the proper performance of test procedures. Report any actual or potential deviation from standard or accepted testing procedures and cooperate fully with any investigation of same. Review and enter test results into the Laboratory Information System for standardized reports to be generated for physician review and interpretation. Maintain laboratory areas and equipment in a safe, functional, and sanitary condition. Complete training and competency checklists as appropriate. Adheres to all established CLIA, HIPAA, OSHA, and laboratory safety requirements. Required to use (a) personal protective equipment, (b) engineering controls, and/or (c) work practice controls as directed by management. Answer questions from clients or other lab personnel, if applicable. Participate in government or regulatory agency inspections, if needed. Other duties as assigned. This is not an exhaustive list of all duties and responsibilities, but rather a general description of work performed by the position. Qualifications
Required Work Experience: Previously qualified as a Technologist under 42 CFR 493.1433 published in March 14, 1990. Preferred Work Experience: One (1) to three (3) years of clinical experience preferred. Physical And Mental Requirements
The normal performance of duties may require lifting and carrying objects: 1 to 10 pounds frequently; 11 to 25 pounds occasionally; 36 to 50 pounds seldom; over 50 pounds not to be lifted without assistance. Ability to stand and work at the bench for long periods of time. Frequent walking and/or standing. May be required to use a wide variety of manual and automated pipettes and laboratory instruments and apparatuses, all demanding significant manual dexterity. Knowledge
Basic theoretical and operational knowledge in clinical testing. Knowledge of organizational/departmental policies and procedures. Skills
Detail-oriented, able to work independently, establish priorities, and handle several tasks simultaneously. Interpersonal skills to work with supervisors, co-workers, and clients. Communication skills to handle telephone inquiries from clients. Ability to handle client information confidentially. Proficiency in Microsoft Office (Word, Excel, Outlook) and Laboratory Information Systems. Education
Associates Degree (Required). Bachelors Degree. LICENSE CERTIFICATIONS:
ASCP Certification. For a full list of Quest Diagnostics careers, please visit: Quest Diagnostics Careers All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. Quest Diagnostics is an Equal Opportunity Employer: Women / Minorities / Veterans / Disabled / Sexual Orientation / Gender Identity / Citizenship. #J-18808-Ljbffr