Medical Laboratory Scientist II

Quest Diagnostics Incorporated

Royal Oak (MI)

On-site

USD 29,913 - 42,603

Full time

14 days+
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Benefits offered by this job

Day 1 medical, supplemental health, dental & vision benefits
401(k) plan with company match
Annual health assessments
Flexible Spending Accounts
Education assistance
Career advancement opportunities

Job summary

A national medical laboratory in Royal Oak, MI, is seeking a Medical Laboratory Scientist II. The role requires proficiency in testing, with responsibilities including troubleshooting, quality control, and compliance with laboratory standards. Preferred candidates will have at least 3 years of clinical experience and a Bachelor's Degree in an appropriate field. The position offers a competitive hourly wage and comprehensive benefits including health insurance, paid time off, and a retirement savings plan.

Qualifications

  • 1 year full-time experience in a clinical laboratory setting.
  • Preferred 3 years clinical experience in the present department.
  • Capacity to lift and carry objects up to 50 pounds with assistance.

Responsibilities

  • Proficient in testing and troubleshooting departmental instruments.
  • Support quality control and troubleshooting complex laboratory issues.
  • Document test results accurately in the Laboratory Information System.

Skills

Leadership and problem-solving skills
Attention to detail
Independent work capability
Interpersonal skills
Communication skills
Proficiency in Microsoft Office
Proficiency in Laboratory Information Systems

Education

Bachelor's Degree in Medical Technology, Biology, or Chemistry
Associate's Degree in Laboratory Science or Medical Technology

Job description

Medical Laboratory Scientist II – Royal Oak, MI

Sunday–Saturday, rotating weekends: 6:30 AM to 3:00 PM

Pay range: $26.32 + per 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.

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+ hours
  • Best‑in‑class well‑being programs
  • Annual, no‑cost health assessment program Blueprint for Wellness
  • healthyMINDS mental health program
  • Vacation and Health/Flex Time
  • 6 Holidays plus 1 "MyDay" off
  • FinFit financial coaching and services
  • 401(k) pre‑tax and/or Roth IRA with company match up to 5% after 12 months of service
  • Employee stock purchase plan
  • Life and disability insurance, plus buy‑up option
  • Flexible Spending Accounts
  • Annual incentive plans
  • Matching gifts program
  • Education assistance through MyQuest for Education
  • Career advancement opportunities
  • and so much more!
Responsibilities
  • Must demonstrate proficiency in all areas of testing and be proficient troubleshooting all applicable instruments/procedures in the department.
  • Provides support to the department in the areas of quality control, troubleshooting complex problems, customer support, instrument and equipment maintenance, staff training, process improvement and the completion of special projects as assigned.
  • Perform and report on assigned analytical tests in accordance with applicable Standard Operating Procedures (SOP) ensuring that applicable quality control requirements are met.
  • 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 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 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.
  • Enter test results into the Laboratory Information System for standardized report 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.
  • May assist supervisor with training of other laboratory personnel.
  • 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.
  • May be required, in the absence of a Supervisor, to assume lead responsibilities if qualified and delegated.
  • 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

One (1) year full‑time experience or training (high complexity testing) in a clinical laboratory setting.

Preferred Work Experience

Minimum of 3 years clinical experience with most current year in present department.

Physical and Mental Requirements
  • The normal performance of duties may require lifting and carrying objects: Objects 1 to 10 pounds are lifted and carried frequently; objects 11 to 25 pounds are lifted and carried occasionally; objects 36 to 50 pounds are seldom lifted or carried and objects over 50 pounds are not to be lifted or carried 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 of which demand significant manual dexterity.
Knowledge
  • Comprehensive theoretical and operational job knowledge in designated specialty required.
  • Knowledge of organizational/departmental policies and procedures.
  • BS/BA in Medical Technology, Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990.
  • Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation). United States‑educated candidates must provide a detailed original transcript.
  • Other state specific requirements may apply depending on BU's state testing certifications. Check with local HR or QA departments.
Skills
  • Proven leadership and problem‑solving skills.
  • Must be detail‑oriented, have the ability to work independently, establish work priorities and to handle several tasks simultaneously for maximum department efficiency.
  • Interpersonal skills necessary to deal courteously and effectively with supervisors, co‑workers and clients.
  • Communication skills necessary to handle telephone inquiries from clients.
  • Ability to deal with client information in a confidential manner.
  • Proficiency in Microsoft Office (Word, Excel and Outlook) and Laboratory Information Systems.
Education
  • Bachelor's Degree BS in Medical Technology, Biology or Chemistry (Preferred)
  • Associate's Degree Laboratory Science or Medical Technology (Preferred)
License / Certificate
  • ASCP Certification (Preferred)

Equal Opportunity Employer: Race/Color/Sex/Sexual Orientation/Gender Identity/Religion/National Origin/Disability/Vets or any other legally protected status.

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