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Sample Processor Jobs (NOW HIRING)

KEEN Footwear

Associate Sample Coordinator

Portland, OR · On-site

$23 - $25/hr

... keep processes running smoothly. Completes day-to-day tasks independently using established ... Handles sample logistics, including receiving, organizing, shipping, and inventory management.

Murata America

Sample Order Support Coordinator

Rockmart, GA · Hybrid

$16.25 - $22/hr

The Sample Coordinator resolves order-related questions, discrepancies, and delays through timely ... Process order changes and cancellations while maintaining accurate customer order information.

Brownhealth

Path Sample Processing Clrk

Providence, RI

$18 - $25.82/hr

Receives specimens for pre-analytical processing (i.e., spinning of bloods, aliquoting of samples, patient registration, test ordering, generating bar code labels, verifying proper labeling of ...

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How much do sample processor jobs pay per hour?

As of Jun 20, 2026, the average hourly pay for sample processor in the United States is $16.74, according to ZipRecruiter salary data. Most workers in this role earn between $13.46 and $19.23 per hour, depending on experience, location, and employer.

What job makes $10,000 a month without a degree?

A sample processor role typically does not pay $10,000 a month without specialized skills or experience. High-paying jobs that can reach this level without a degree often include sales, real estate, or certain entrepreneurial ventures, but these usually require significant effort, expertise, or licensing. Most roles with such earnings involve advanced skills, certifications, or business ownership rather than entry-level positions.

What jobs in the US pay 300,000 a year?

Sample processors typically do not earn $300,000 annually; high-paying roles in the US that reach this level include specialized medical surgeons, anesthesiologists, corporate executives, and certain technology executives. These positions often require advanced degrees, extensive experience, and leadership responsibilities.

What are some typical challenges a Sample Processor might encounter in their daily work, and how can they be addressed?

Sample Processors often face challenges such as handling a high volume of samples while maintaining strict accuracy and contamination control. Managing time efficiently and adhering to detailed protocols are essential, as even small errors can impact test results. To address these challenges, it's important to stay organized, double-check work, and communicate effectively with lab colleagues to ensure smooth workflow. Many labs provide ongoing training and support to help Sample Processors stay current with best practices and safety standards.

How long does it take to become a specimen processor?

Becoming a specimen processor typically requires a high school diploma or equivalent and can take a few weeks to a few months, depending on the training program or employer requirements. On-the-job training is common, and familiarity with laboratory tools and safety protocols is beneficial for quick onboarding.

What is the difference between Sample Processor vs Laboratory Technician?

AspectSample ProcessorLaboratory Technician
CredentialsHigh school diploma or equivalent; training in sample handlingHigh school diploma; often additional certifications in lab procedures
Work EnvironmentProcessing areas, laboratories, manufacturing facilitiesLaboratories, research centers, clinical settings
Industry UsageManufacturing, food processing, environmental testingHealthcare, research, diagnostics
Job FocusPreparing and processing samples for testing or analysisPerforming tests, recording data, maintaining lab equipment

While both roles involve working with samples, Sample Processors primarily focus on preparing samples for analysis, whereas Laboratory Technicians perform testing and data recording. The roles often overlap in credentials and work environment, but their specific duties differ based on industry needs.

How to be a specimen processor?

To become a specimen processor, you typically need a high school diploma or equivalent and training in laboratory procedures. The role involves handling, labeling, and preparing biological samples using tools like centrifuges and pipettes, often requiring attention to detail and adherence to safety protocols. Some positions may require certification or on-the-job training.

What are sample processors?

Sample processors are professionals who handle, prepare, and manage samples—such as biological specimens, chemical substances, or environmental materials—for analysis in laboratory or research settings. Their duties typically include labeling, sorting, storing, and sometimes performing preliminary tests on samples to ensure their integrity and traceability. Sample processors play a crucial role in maintaining quality control and supporting accurate laboratory results. They follow strict safety protocols and documentation procedures to prevent contamination and ensure compliance with regulations.

What are the key skills and qualifications needed to thrive as a Sample Processor, and why are they important?

To thrive as a Sample Processor, you need attention to detail, organizational skills, and a basic understanding of laboratory procedures, often supported by a high school diploma or equivalent. Familiarity with laboratory information management systems (LIMS), sample tracking software, and standard lab equipment is typically required. Strong communication, time management, and the ability to follow strict protocols set outstanding Sample Processors apart. These skills ensure accurate sample handling, data integrity, and efficient workflow in laboratory environments.
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Technician I, Sample Processing

Technician I, Sample Processing

Charles River Laboratories, Inc.

Ashland, OH

$19/hr

Full-time

Medical, Retirement, PTO

Posted 19 hours ago

Charles River Laboratories rating

8.2

Company rating: 8.2 out of 10

Based on 91 frontline employees who took The Breakroom Quiz

25th of 71 rated pharmaceutical

Job description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Overview

BASIC SUMMARY:

Prepare study materials and study books prior to sample processing collection days. Operate basic to moderately complex equipment and process toxicokinetic samples. Assist in the performance and review of study ordered parameters and computer input of raw data.

ESSENTIAL RESPONSIBILITIES:

  • Prepare materials needed, including tubes, study books and appropriate paperwork prior to sample.
  • Process, check, and store samples for analysis.
  • Review documentation of functions performed as part of quality control requirements.
  • Perform daily maintenance and quality control of minimal to moderately complex equipment, with minimal supervision.
  • Assist with inventory of laboratory supplies.
  • Perform all other related duties as assigned.
  • Train in all SPL functions to gain proficiency and independence in skill set.

The pay for this position is $19/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Description

QUALIFICATIONS:

  • Education: High school diploma or General Education Degree (G.E.D.) preferred. 
  • Experience: No previous experience required.
  • An equivalent combination of education and experience may be accepted as a satisfactory. substitute for the specific education and experience listed above.
  • Certification/Licensure: None, unless required by local government.
  • Excellent written and verbal communication skills.
  • Ability to manage multiple tasks and priorities to achieve goals.
  • Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
  • Must be authorized to work in United States without a sponsor visa now or in the future.

PHYSICAL DEMANDS:

  • Must be able to perform procedures, which require, talking, hearing, walking, or standing for long     periods of time (75% of the workday), entering data into a computer, using appropriate instruments,     reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE)     according to OSHA regulations and company standards.
  • Specific vision abilities required by this job include close vision, color vision, depth perception, and     the ability to adjust focus.
  • Must be able to lift, move, manipulate, and/or hold heavy objects up to and including 30 pounds.

WORK ENVIRONMENT:

  • Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
  • Fine motor skills and hand dexterity to processing micro/mini- samples, which may require quality eyesight or corrective lenses
  • Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.

COMMENTS:

  • Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
  • Ability to work under specific time constraints.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market.  Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.


About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life.  Based on your position these may include:  bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

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About Charles River

Sourced by ZipRecruiter

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947

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