| Job Description 
 Medical Laboratory Scientist - Quality Control - Clifton, NJ, Monday to Friday, 9:00 AM to 5:30 PM Department - Clinical Laboratory - Auto Chemistry Pay range: $33.00 - $54.45 / hour Salary offers are based on a wide range of factors including relevant skills, training, experience, education, and, where applicable, certifications obtained. Market and organizational factors are also considered. Successful candidates may be eligible to receive annual performance bonus compensation. Benefits information:
 We are proud to offer best-in-class benefits and programs to support employees and their families in living healthy, happy lives. Our pay and benefit plans have been designed to promote employee health in all respects - physical, financial, and developmental. Depending on whether it is a part-time or full-time position, some of the benefits offered may include:
 
 
 
 Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hoursBest-in-class well-being programsAnnual, no-cost health assessment program Blueprint for WellnesshealthyMINDS mental health programVacation and Health/Flex Time6 Holidays plus 1 "MyDay" offFinFit financial coaching and services401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of serviceEmployee stock purchase planLife and disability insurance, plus buy-up optionFlexible Spending AccountsAnnual incentive plansMatching gifts programEducation assistance through MyQuest for EducationCareer advancement opportunitiesand so much more!
 
 Monitor, coordinate, and/or perform quality control/ quality assurance activities within a defined laboratory. Provides support for laboratory technical and non-technical staff in order to expedite workflow and aides in the resolution of technical problems. Has a fundamental understanding of Specimen Processing, test performance, and reporting test results for all tests performed in laboratory supported. 
 Responsibilities:
 
 
 Must demonstrate proficiency in all principle duties of a Medical Technologist I and / or II.Manages/ coordinates activities defined on the department's "Quality Scheduler".Maintains LIS based QC software program including development of quality control (QC) targets and ranges. Periodically reviews/ adjusts QC performance limits.Manages/ coordinates parallel testing events for both new reagent and quality control materials.Manages all facets of both Internal and External proficiency testing programs; including pre-analytical handling, compiling and completing PT submission forms, cataloging PT responses, maintaining inventory of previously assayed PT materials. Coordinates and summarizing root cause investigations following sub-optimal performance.Maintains document control for all records generated during routine laboratory testing.Key resource for ensuring continues compliance with external regulatory agencies. Reviews unit activities to ensure compliance with departmental policies and federal, state, and local regulations.Involved in the management of training and competency documents.Works with supervisor/ department manager, providing support during the validation of new procedures.Reviews QA and QC records when applicable.Serve as a technical resource for the unit by investigating and resolving analytical testing problems. Recommending a course of action in instances identified as beyond acceptable limits, and responding to non-routine/complex inquiries and/or requests from clients and sales representatives.Review requests for validity checks and recommend an appropriate course of action taking into account the limitations of specimen requirements and the effects of time and the quality of additional and/or repeat testing.Assist with the department's annual competency testing process and documentation.Interact in a professional manner with inter-departmental teams and groups.Perform other duties as directed by department managerMust interact with other departments.Contact with clients will be required, good customer service skills important.Interaction with purchasing and manufacturer technical representatives.Must protect patient confidentiality at all times.
 
 Qualifications:
 Required Work Experience: Minimum of five years clinical experience with two years in present department. Preferred Work Experience: N/A Physical and Mental Requirements: N/A Knowledge: N/A Skills: 
 Good customer service skills important.Must have the ability to establish work priorities for self and others and handle several procedures simultaneously including troubleshooting instruments and other problems/issues.Ability to schedule and manage resources to meet department goals Education: Associates Degree (Required)Bachelor's Degree
 
 46706
 
 Quest Diagnostics honors our service members and encourages veterans to apply.
 
 While we appreciate and value our staffing partners, we do not accept unsolicited resumes from agencies. Quest will not be responsible for paying agency fees for any individual as to whom an agency has sent an unsolicited resume.
 
 Equal Opportunity Employer: Race/Color/Sex/Sexual Orientation/Gender Identity/Religion/National Origin/Disability/Vets or any other legally protected status.
 |