Rocky Mountain Laboratories LLC
Core Lab Supervisor – Clinical Chemistry
Rocky Mountain Laboratories – Tempe, AZ
About Us Rocky Mountain Laboratories is a clinical laboratory providing comprehensive laboratory services with a focus on molecular diagnostics, infectious disease testing, toxicology, and core laboratory operations. We are dedicated to delivering accurate and timely diagnostic information and are committed to improving healthcare outcomes through cutting‑edge technology and a customer‑focused approach.
Position Rocky Mountain Laboratories is seeking an experienced Core Lab Supervisor – Clinical Chemistry to oversee daily operations of the clinical chemistry, hematology, immunology, and coagulation departments at our Tempe, AZ laboratory. This role is ideal for a hands‑on laboratory leader with strong technical expertise and prior supervisory experience in a regulated clinical laboratory environment.
The Core Lab Supervisor will support laboratory startup and ongoing operations, lead staff training, establish workflows, maintain instrumentation, and develop and update standard operating procedures (SOPs) in compliance with CLIA and CAP requirements. This position plays a key role in ensuring high‑quality, compliant, and timely laboratory testing services.
Schedule Tuesday through Saturday, 9:00 a.m. – 5:00 p.m. (Some flexibility may be required based on operational needs.)
Responsibilities
Supervise and lead daily core laboratory operations, including clinical chemistry, hematology, immunology, and coagulation testing
Provide hands‑on technical support and training to laboratory staff, including manual differentials, peripheral blood smears, microscopy, and urinalysis (UAs)
Maintain and troubleshoot chemistry and hematology analyzers, including Beckman Coulter 480/680, Abbott Alinity, Sysmex hematology systems, and ACL Elite coagulation instruments
Organize and implement workflows and operational processes to support laboratory growth, efficiency, and scalability
Create, review, and update standard operating procedures (SOPs) in accordance with CLIA, CAP, and internal quality standards
Support laboratory validation activities and documentation, including method verification and implementation support
Ensure accurate, timely, and compliant testing services while maintaining quality, productivity, and turnaround time standards
Monitor quality control (QC), quality assurance (QA), and proficiency testing (PT) activities and assist with trend review and corrective actions
Support training documentation, competency assessments, and ongoing technical education for laboratory staff
Assist with inspection readiness, audits, and corrective action plans as needed
Partner with laboratory leadership on continuous process improvement and operational optimization initiatives
Ensure appropriate documentation, record retention, and regulatory compliance in accordance with laboratory requirements
Serve as a technical resource and supervisory designee as applicable under CLIA regulations
Other duties as assigned by ownership
Required Qualifications
Minimum of 3 years of experience in a supervisory role within a core laboratory environment
Bachelor’s degree in Clinical Laboratory Science, Chemistry, Biology, or a related scientific field
ASCP certification (MLS/MT/MLT) or higher credential
Extensive hands‑on experience with peripheral smears, manual differentials, microscopy, and urinalysis
Working knowledge of CLIA regulations and clinical laboratory compliance requirements
Demonstrated ability to lead, train, and support laboratory staff in a high‑throughput, regulated environment
Strong organizational skills with the ability to establish workflows and develop or revise SOPs
Excellent communication, leadership, and problem‑solving skills
Preferred Qualifications
Strong hands‑on experience with Abbott Alinity chemistry and immunology analyzers
Familiarity with Sysmex hematology analyzers
Experience with ACL Elite coagulation instruments
Experience supporting laboratory startup, expansion, or new test implementation
Validation experience, including method verification or analyzer validation
Experience supporting CAP inspections or CLIA surveys
Familiarity with laboratory information systems (LIS), analyzer interfacing, and result verification workflows
Job Type Full‑Time, W2
Salary $95,000 – $105,000 per year, depending on experience
Benefits for full‑time W2 Team Members Benefits begin 60 days after the first full month of full‑time employment.
Health, Dental, and Vision Insurance
Paid Time Off (21 days annually for full‑time team members)
7 Paid Holidays
401(k) with 50% Company Match up to 6% ***
Health Savings Account (HSA)
Short‑Term & Long‑Term Disability (RML covers 60% of STD premium) ***
Voluntary Life and AD&D Insurance
100% Company‑Funded Employee Assistance Program (EAP) ***
Ability to commute/relocate Tempe, AZ: Reliably commute or plan to relocate before starting work (Required)
Relocation Assistance Available and variable for qualified candidates
Ideal start date Whenever we find the right candidate
If you meet the above qualifications and are interested in joining our team, please submit your resume for consideration. We look forward to hearing from you!
At Rocky Mountain Laboratories, we prioritize the care and well‑being of our team members.
Equal Opportunity Employer Statement Rocky Mountain Laboratories is an Equal Opportunity Employer committed to diversity in its workforce. We comply with all applicable federal and state laws and prohibit discrimination based on race, ethnicity, religion, color, national origin, sex, age, sexual orientation, gender identity or expression, veteran status, disability, or genetic information. We also comply with the Americans with Disabilities Act (ADA) and provide reasonable accommodations to qualified individuals with disabilities.
Pre‑Employment Notice & E‑Verify Rocky Mountain Laboratories participates in E‑Verify. Employment is contingent upon successful completion of a background check and other pre‑employment screenings, as required.
Employment at‑will Employment with Rocky Mountain Laboratories is at‑will. This means either the Team Member or the company may end the employment relationship at any time, with or without cause or notice, in accordance with applicable laws. Nothing in this posting or in future communications alters that relationship.
Agency Statement While we appreciate interest from staffing agencies, Rocky Mountain Laboratories does not currently partner with external agencies. Resumes submitted unsolicited will not be considered, and no fees will be paid.
Links
www.linkedin.com/company/rocky-mountain-laboratories
www.indeed.com/cmp/Rocky-Mountain-Laboratories
www.rockylabs.com/
#J-18808-Ljbffr
About Us Rocky Mountain Laboratories is a clinical laboratory providing comprehensive laboratory services with a focus on molecular diagnostics, infectious disease testing, toxicology, and core laboratory operations. We are dedicated to delivering accurate and timely diagnostic information and are committed to improving healthcare outcomes through cutting‑edge technology and a customer‑focused approach.
Position Rocky Mountain Laboratories is seeking an experienced Core Lab Supervisor – Clinical Chemistry to oversee daily operations of the clinical chemistry, hematology, immunology, and coagulation departments at our Tempe, AZ laboratory. This role is ideal for a hands‑on laboratory leader with strong technical expertise and prior supervisory experience in a regulated clinical laboratory environment.
The Core Lab Supervisor will support laboratory startup and ongoing operations, lead staff training, establish workflows, maintain instrumentation, and develop and update standard operating procedures (SOPs) in compliance with CLIA and CAP requirements. This position plays a key role in ensuring high‑quality, compliant, and timely laboratory testing services.
Schedule Tuesday through Saturday, 9:00 a.m. – 5:00 p.m. (Some flexibility may be required based on operational needs.)
Responsibilities
Supervise and lead daily core laboratory operations, including clinical chemistry, hematology, immunology, and coagulation testing
Provide hands‑on technical support and training to laboratory staff, including manual differentials, peripheral blood smears, microscopy, and urinalysis (UAs)
Maintain and troubleshoot chemistry and hematology analyzers, including Beckman Coulter 480/680, Abbott Alinity, Sysmex hematology systems, and ACL Elite coagulation instruments
Organize and implement workflows and operational processes to support laboratory growth, efficiency, and scalability
Create, review, and update standard operating procedures (SOPs) in accordance with CLIA, CAP, and internal quality standards
Support laboratory validation activities and documentation, including method verification and implementation support
Ensure accurate, timely, and compliant testing services while maintaining quality, productivity, and turnaround time standards
Monitor quality control (QC), quality assurance (QA), and proficiency testing (PT) activities and assist with trend review and corrective actions
Support training documentation, competency assessments, and ongoing technical education for laboratory staff
Assist with inspection readiness, audits, and corrective action plans as needed
Partner with laboratory leadership on continuous process improvement and operational optimization initiatives
Ensure appropriate documentation, record retention, and regulatory compliance in accordance with laboratory requirements
Serve as a technical resource and supervisory designee as applicable under CLIA regulations
Other duties as assigned by ownership
Required Qualifications
Minimum of 3 years of experience in a supervisory role within a core laboratory environment
Bachelor’s degree in Clinical Laboratory Science, Chemistry, Biology, or a related scientific field
ASCP certification (MLS/MT/MLT) or higher credential
Extensive hands‑on experience with peripheral smears, manual differentials, microscopy, and urinalysis
Working knowledge of CLIA regulations and clinical laboratory compliance requirements
Demonstrated ability to lead, train, and support laboratory staff in a high‑throughput, regulated environment
Strong organizational skills with the ability to establish workflows and develop or revise SOPs
Excellent communication, leadership, and problem‑solving skills
Preferred Qualifications
Strong hands‑on experience with Abbott Alinity chemistry and immunology analyzers
Familiarity with Sysmex hematology analyzers
Experience with ACL Elite coagulation instruments
Experience supporting laboratory startup, expansion, or new test implementation
Validation experience, including method verification or analyzer validation
Experience supporting CAP inspections or CLIA surveys
Familiarity with laboratory information systems (LIS), analyzer interfacing, and result verification workflows
Job Type Full‑Time, W2
Salary $95,000 – $105,000 per year, depending on experience
Benefits for full‑time W2 Team Members Benefits begin 60 days after the first full month of full‑time employment.
Health, Dental, and Vision Insurance
Paid Time Off (21 days annually for full‑time team members)
7 Paid Holidays
401(k) with 50% Company Match up to 6% ***
Health Savings Account (HSA)
Short‑Term & Long‑Term Disability (RML covers 60% of STD premium) ***
Voluntary Life and AD&D Insurance
100% Company‑Funded Employee Assistance Program (EAP) ***
Ability to commute/relocate Tempe, AZ: Reliably commute or plan to relocate before starting work (Required)
Relocation Assistance Available and variable for qualified candidates
Ideal start date Whenever we find the right candidate
If you meet the above qualifications and are interested in joining our team, please submit your resume for consideration. We look forward to hearing from you!
At Rocky Mountain Laboratories, we prioritize the care and well‑being of our team members.
Equal Opportunity Employer Statement Rocky Mountain Laboratories is an Equal Opportunity Employer committed to diversity in its workforce. We comply with all applicable federal and state laws and prohibit discrimination based on race, ethnicity, religion, color, national origin, sex, age, sexual orientation, gender identity or expression, veteran status, disability, or genetic information. We also comply with the Americans with Disabilities Act (ADA) and provide reasonable accommodations to qualified individuals with disabilities.
Pre‑Employment Notice & E‑Verify Rocky Mountain Laboratories participates in E‑Verify. Employment is contingent upon successful completion of a background check and other pre‑employment screenings, as required.
Employment at‑will Employment with Rocky Mountain Laboratories is at‑will. This means either the Team Member or the company may end the employment relationship at any time, with or without cause or notice, in accordance with applicable laws. Nothing in this posting or in future communications alters that relationship.
Agency Statement While we appreciate interest from staffing agencies, Rocky Mountain Laboratories does not currently partner with external agencies. Resumes submitted unsolicited will not be considered, and no fees will be paid.
Links
www.linkedin.com/company/rocky-mountain-laboratories
www.indeed.com/cmp/Rocky-Mountain-Laboratories
www.rockylabs.com/
#J-18808-Ljbffr