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New · posted Oct 15

Epredia · Medical Devices

Quality Assurance Laboratory Technician II

  • Kalamazoo, MI
  • On-site
  • Full-time
  • Associate & Specialist
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EmploymentFull-time
Deadline

Open until filled

The role

Make a Meaningful Impact

Ready to join a team where your work makes a daily difference in healthcare?

Epredia is a global leader in precision cancer diagnostics solutions. In fact, every second, our products are used 48 times in labs and medical facilities around the world.

We are a proud member of PHC Group, a global collection of companies committed to delivering precision technology for the future of healthcare, from specialized medical equipment to health IT systems to research tools.

Title: Quality Assurance Lab Technician II

Work Arrangement: Onsite - 7:00AM - 3:30PM M-F

Employment Type: Full-Time The Opportunity

We are seeking a skilled and detail-oriented Histologist to join our fast-paced Quality Lab team. In this role, you will perform critical quality control testing on raw materials, bulk formulations, and finished goods to ensure compliance with ISO 13485 standards before products are released to consumers. Beyond routine quality control, you will collaborate directly with our Research and Development (R&D) team to test new raw materials and help optimize product formulas.

Bring Your Expertise

  • Associate or Bachelor’s degree in Histotechnology, Medical Laboratory Science, Biology, Chemistry, or a related scientific field is preferred.
  • HT (ASCP) or HTL (ASCP) certification is highly preferred but not required with equivalent industry experience.
  • 2+ years of experience in a clinical histology lab or a regulated manufacturing quality control environment (ISO 13485, FDA21 CFR Part 820, or GMP).
  • Strong proficiency in manual staining, microtomy (cutting), and embedding. Experience evaluating stain quality, color intensity, and tissue morphology under a microscope.
  • Familiarity with a wide range of histological reagents, fixatives, and solvents.

What you need

What you'll do

How You'll Make An Impact

  1. Test raw materials, in-process bulk chemical formulations, and finished products against strict release specifications.
  2. Perform manual staining techniques exactly as prescribed by Instructions for Use (IFU) documents to verify product efficacy and visual quality.
  3. Utilize standard histology techniques (grossing, embedding, microtomy, and slide preparation) to test the functionality of our manufacturing reagents and waxes.
  4. Record all test results accurately in compliance with Good Documentation Practices (GDP), Standard Operating Procedures (SOPs), and Work Instructions (WINs).
  5. Work alongside R&D scientists to evaluate and tweak chemical formulations for improved performance or cost-efficiency.
  6. Test and validate new or alternative raw materials to ensure they meet performance and regulatory standards.
  7. Maintain strict adherence to medical device quality management system (QMS) requirements and participate in internal/external audits as needed.
  8. Coordinate closely with the manufacturing team in a high-throughput environment to minimize production bottlenecks and support timely product releases.

Ready to Make an Impact?

If this opportunity aligns with your skills and career goals, we'd love to hear from you. Apply today and take the next step in your career with us.

Where you'll work

Kalamazoo, MIOn-siteOpen in Maps (opens in a new tab)

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Building an Inclusive Culture

We are a company that brings the best people together and leverages their varying backgrounds, ideas, and points of view to invent on behalf of all customers. We are committed to equal employment opportunity for all individuals, without regard to race, color, national origin, ancestry, sex, age, religion, physical or mental disability, medical condition, veteran status, marital status, pregnancy, sexual orientation, gender identity, genetic information, or any other protected classes which may exist under applicable federal, state, or local law.

Job intelligence

The context around this role

Live data · October 15, 2026

Salary intelligence

How the pay compares

Associate & Specialist roles in the US100 roles publishing pay

Middle half $49,375 to $76,125, median $60,000
Annual base pay
Annual base payLowMedianHigh
All US$49,375$60,000$76,125

Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Control

The general path across 275 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Epredia's own promotion track.

  1. This role

    Associate & Specialist

    Often: Quality Inspector · Quality Control Inspector

    $60K median149 open
  2. Next step

    Senior & Principal

    Often: Scientist, Quality Control · Senior Scientist, Quality Control

    $95K median70 open
  3. Later

    Manager

    Often: Quality Control Manager · Manager Quality Control

    $127K median31 open
  4. Later

    Director

    Often: Associate Director, Quality Control · Senior Director, Quality Control

    $199K median25 open

Skills DNA

What this role leans on

How many of the posting's 21 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 4 linesLab testing and methods: 6 linesDocumentation and SOPs: 2 linesValidation and qualification: 1 lineQuality systems and risk: 3 linesCollaboration and leadership: 4 linesGMPLab testingDocumentationValidationQuality systemsTeamwork
  • Lab testing and methods6
  • GMP and compliance4
  • Collaboration and leadership4
  • Quality systems and risk3
  • Documentation and SOPs2
  • Validation and qualification1

Company hiring pulse

Epredia on Regulatory Jobs

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See all 1 Epredia roles

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Quality Assurance Laboratory Technician II at Epredia

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    Quality Assurance Laboratory Technician II at Epredia — Kalamazoo, MI | Regulatory Jobs