LC-MS/MS Sample Prep & Data Review Specialist

Clinical Reference Laboratory; Lenexa (KS); On-site; USD 33,000 - 63,000; Full time

Benefits offered by this job

Medical, Dental, Vision

Life/AD&D

401(k)

Paid Time Off

Holidays

Tuition Reimbursement

Job summary

Clinical Reference Laboratory in Lenexa, KS seeks a Confirmation Chemist at multiple levels to support LC-MS/MS, GC-FID, and Q-TOF workflows. You will handle sample prep, data review, and maintain chain of custody in a fast-paced laboratory.

Levels 1–4 define increasing responsibilities, including instrument operation, data review, and batch certification. The role requires strong attention to detail, compliance with safety regs, and timely processing to meet production goals.

Qualifications

• Education: degree in medical technology, clinical laboratory, chemical, physical, or biological science or equivalent.
• Moderate to high complexity testing experience required.
• Ability to operate and maintain LC-MS/MS, GC-FID, and Q-TOF instrumentation.

Responsibilities

• Receive and prepare samples for instrumentation.
• Maintain chain of custody throughout process.
• Read and follow laboratory SOPs.
• Ensure timely processing and quality improvements.
• Operate, monitor, and document LC-MS/MS, GC-FID, and Q-TOF instruments.

Skills

Communication skills

Organizational skills

Time management

Attention to detail

Decision making

Follow instructions

Laboratory technique

Punctuality

Team communication

Education

Relevant degree (Medical Technology / Clinical Laboratory / Chemistry / Biology)

Tools

LC-MS/MS

GC-FID

Q-TOF

Tecan

Pipettors

Balance

Evaporation manifolds

Heat blocks

Temperature monitoring

Glassware

Job description

Clinical Reference Laboratory in Lenexa, KS seeks a Confirmation Chemist at multiple levels to support LC-MS/MS, GC-FID, and Q-TOF workflows. You will handle sample prep, data review, and maintain chain of custody in a fast-paced laboratory.

Levels 1–4 define increasing responsibilities, including instrument operation, data review, and batch certification. The role requires strong attention to detail, compliance with safety regs, and timely processing to meet production goals.