Quest Diagnostics Incorporated
Job Description
Quest Diagnostics is hiring a Blood Bank Supervisor in Hackensack, NJ. This is a hospital-based position.
Shift:
Monday to Friday, 8:00 AM to 5:00 PM, with weekends and holidays as needed
Responsible for the scheduling and supervision of the non-exempt lab personnel on multiple shifts. Accountable for quantity and quality of specimens handled and test results.
Pay range:
$84,040 - $151,360 / year
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
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
Oversees staff and activities of the department, distributes/assigns work; determines priorities; schedules non‑routine procedures; performs personnel related functions (hiring, firing, discipline, training, etc.).
Performs advanced/specialized tests and other related laboratory techniques. May duplicate work of others to confirm test results. Re‑evaluates methodology, makes recommended changes and assists in test interpretation. Determines if further testing should be done on samples or if test should be repeated.
Checks/approves all specialized and problem reports for accuracy, following up with appropriate correct action.
Initiates quality‑control measures and monitors quality of work for adherence to laboratory standards.
Performs duties of technologist as necessitated by absence or peak workload.
Completes special projects as requested, e.g., state, national, and/or blood supplier surveys, statistical reports, studies, research, etc.
Must be knowledgeable of AABB, CAP FDA (cGMP) and NJDOH regulatory guidelines for the Transfusion Service and Blood Center.
Performance Improvement & Quality Assurance
Compile and maintain data for process improvement (PI) dashboards as per Quest, Hospital, and/or regulatory needs.
Investigate any PI outliers, create corrective action plans, audit said corrective actions, and deem its efficacy.
Review non‑conformances, unplanned deviations from policy, and act upon as deemed appropriate or necessary.
People Management
Perform recruitment, interviewing and on‑boarding tasks to successfully bring in new team members.
Supervise new team member training throughout the Transfusion Service to ensure competence through stringent assessment prior to working independently.
Schedule all clinical laboratory team members, ensure correct balance of skills within all lab benches daily while maintaining FTE budget.
Address performance problems using defined disciplinary process to ensure compliance with Quest lab and HMH policies.
Perform annual performance assessments for all assigned team members to include comprehensive review of year's work.
For new employees, ensure required 6‑month assessments are performed and staff is deemed competent in applicable task(s).
Technical Expertise
Expert troubleshooting in all phases of Transfusion Service testing including instruments, equipment, reagents, testing methodology and LIS.
Continually maintain a state of inspection‑readiness for AABB, CAP, and NJDOH by ensuring all QC and QA tasks are performed accurately and according to a defined policy and schedule.
Review and ensure department is complemented with any new or revised standards or regulations published at defined intervals.
Design and implement an appropriate validation plan of new equipment, reagent(s), or significant workflow initiative.
Perform method‑to‑method correlation studies or tests according to regulatory standards.
Seek out and investigate opportunities for advancement or improvement of the equipment or technology used in the Transfusion Service.
Policies and Procedures
Develop and coordinate the implementation of new protocols, policies, and procedures.
Ensure document control is always maintained to meet regulatory requirements.
Ensure annual review of SOPs with appropriate documentation.
Qualifications Required Work Experience:
Minimum of 5+ years in Immunohematology/Blood Bank.
Preferred Work Experience:
Previous Supervisory experience preferred.
Blood Donor Center experience preferred.
Physical and Mental Requirements:
Ability to sit and stand for long periods of time.
Knowledge:
Knowledge of AABB, CAP and FDA regulatory guidelines for the Transfusion Service and Blood Center.
Skills:
Ability to work with hospital and laboratory personnel in meeting the standards for clinical testing
Ability to lead subordinate staff in the performance of their duties.
Ability to work with and communicate effectively with physicians, hospital and company leadership, staff, and customers.
Ability to manage multiple engagements concurrently.
Strong interpersonal and presentation skills.
Ability to work in a very dynamic team environment.
Strong client interaction skills.
Excellent verbal and written communication skills.
Education:
BS in Medical Technology preferred; or BS/BA in Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493
51825
Quest Diagnostics honors our service members and encourages veterans to apply.
Equal Opportunity Employer: Race/Color/Sex/Sexual Orientation/Gender Identity/Religion/National Origin/Disability/Vets or any other legally protected status.
#J-18808-Ljbffr
Shift:
Monday to Friday, 8:00 AM to 5:00 PM, with weekends and holidays as needed
Responsible for the scheduling and supervision of the non-exempt lab personnel on multiple shifts. Accountable for quantity and quality of specimens handled and test results.
Pay range:
$84,040 - $151,360 / year
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
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
Oversees staff and activities of the department, distributes/assigns work; determines priorities; schedules non‑routine procedures; performs personnel related functions (hiring, firing, discipline, training, etc.).
Performs advanced/specialized tests and other related laboratory techniques. May duplicate work of others to confirm test results. Re‑evaluates methodology, makes recommended changes and assists in test interpretation. Determines if further testing should be done on samples or if test should be repeated.
Checks/approves all specialized and problem reports for accuracy, following up with appropriate correct action.
Initiates quality‑control measures and monitors quality of work for adherence to laboratory standards.
Performs duties of technologist as necessitated by absence or peak workload.
Completes special projects as requested, e.g., state, national, and/or blood supplier surveys, statistical reports, studies, research, etc.
Must be knowledgeable of AABB, CAP FDA (cGMP) and NJDOH regulatory guidelines for the Transfusion Service and Blood Center.
Performance Improvement & Quality Assurance
Compile and maintain data for process improvement (PI) dashboards as per Quest, Hospital, and/or regulatory needs.
Investigate any PI outliers, create corrective action plans, audit said corrective actions, and deem its efficacy.
Review non‑conformances, unplanned deviations from policy, and act upon as deemed appropriate or necessary.
People Management
Perform recruitment, interviewing and on‑boarding tasks to successfully bring in new team members.
Supervise new team member training throughout the Transfusion Service to ensure competence through stringent assessment prior to working independently.
Schedule all clinical laboratory team members, ensure correct balance of skills within all lab benches daily while maintaining FTE budget.
Address performance problems using defined disciplinary process to ensure compliance with Quest lab and HMH policies.
Perform annual performance assessments for all assigned team members to include comprehensive review of year's work.
For new employees, ensure required 6‑month assessments are performed and staff is deemed competent in applicable task(s).
Technical Expertise
Expert troubleshooting in all phases of Transfusion Service testing including instruments, equipment, reagents, testing methodology and LIS.
Continually maintain a state of inspection‑readiness for AABB, CAP, and NJDOH by ensuring all QC and QA tasks are performed accurately and according to a defined policy and schedule.
Review and ensure department is complemented with any new or revised standards or regulations published at defined intervals.
Design and implement an appropriate validation plan of new equipment, reagent(s), or significant workflow initiative.
Perform method‑to‑method correlation studies or tests according to regulatory standards.
Seek out and investigate opportunities for advancement or improvement of the equipment or technology used in the Transfusion Service.
Policies and Procedures
Develop and coordinate the implementation of new protocols, policies, and procedures.
Ensure document control is always maintained to meet regulatory requirements.
Ensure annual review of SOPs with appropriate documentation.
Qualifications Required Work Experience:
Minimum of 5+ years in Immunohematology/Blood Bank.
Preferred Work Experience:
Previous Supervisory experience preferred.
Blood Donor Center experience preferred.
Physical and Mental Requirements:
Ability to sit and stand for long periods of time.
Knowledge:
Knowledge of AABB, CAP and FDA regulatory guidelines for the Transfusion Service and Blood Center.
Skills:
Ability to work with hospital and laboratory personnel in meeting the standards for clinical testing
Ability to lead subordinate staff in the performance of their duties.
Ability to work with and communicate effectively with physicians, hospital and company leadership, staff, and customers.
Ability to manage multiple engagements concurrently.
Strong interpersonal and presentation skills.
Ability to work in a very dynamic team environment.
Strong client interaction skills.
Excellent verbal and written communication skills.
Education:
BS in Medical Technology preferred; or BS/BA in Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493
51825
Quest Diagnostics honors our service members and encourages veterans to apply.
Equal Opportunity Employer: Race/Color/Sex/Sexual Orientation/Gender Identity/Religion/National Origin/Disability/Vets or any other legally protected status.
#J-18808-Ljbffr