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Quality Control Sample Coordinator Jobs (NOW HIRING)

$20.75 - $28/hr

This role is also responsible for coordinating with key internal stakeholders on the transport of QC samples from Holly Springs to external testing laboratories and support continuous improvement ...

Sample Coordinator

Burlington, NC · On-site

$15.25 - $20.75/hr

Sample Coordinator Support the Sales & Design departments by managing sample creation, stock ... Work with Design to verify quality and additional product specifications. * Track and ship sales ...

Sample Coordinator

Burlington, NC · On-site

$15.25 - $20.75/hr

Work with Design to verify quality and additional product specifications. * Track and ship sales ... Experience in sample coordination and/or inventory management preferred. * Strong organizational ...

About the Role We're looking for a highly organized, detail-oriented Sample Coordinator to support ... Flag delays, quality issues, or discrepancies and help drive quick resolutions What You Bring * 1-3 ...

We are seeking an experienced QC Sampler to join our team in the Miramar area . This position plays a key role in the quality control process by ensuring that products meet established standards ...

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Quality Control Sample Coordinator information

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How much do quality control sample coordinator jobs pay per hour?

As of May 30, 2026, the average hourly pay for quality control sample coordinator in the United States is $23.51, according to ZipRecruiter salary data. Most workers in this role earn between $18.99 and $26.20 per hour, depending on experience, location, and employer.

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

To thrive as a Quality Control Sample Coordinator, you need strong organizational skills, attention to detail, and a background in life sciences or a related field, often supported by relevant laboratory experience. Familiarity with laboratory information management systems (LIMS), sample tracking software, and standard operating procedures (SOPs) is typically required. Excellent communication, problem-solving abilities, and time management help you manage priorities and collaborate with cross-functional teams. These skills and qualities are essential to ensure accurate sample handling, regulatory compliance, and efficient laboratory operations.

What are some common challenges faced by a Quality Control Sample Coordinator, and how can they be addressed?

Quality Control Sample Coordinators often face challenges related to managing multiple samples with tight deadlines, ensuring proper documentation, and maintaining compliance with regulatory standards. Staying organized and using laboratory information management systems (LIMS) can help streamline sample tracking and minimize errors. Additionally, effective communication with laboratory staff and other departments is crucial for timely processing and resolving any discrepancies that may arise. Adhering to standard operating procedures and continuous training can further reduce the risk of mistakes and ensure high-quality outcomes.

What does a Quality Control Sample Coordinator do?

A Quality Control Sample Coordinator is responsible for managing and organizing samples that are tested for quality assurance in manufacturing or laboratory environments. They receive, log, label, store, and distribute samples to the appropriate departments for analysis. Additionally, they maintain accurate records, track sample status, and ensure compliance with regulatory and company standards. This role is crucial for ensuring that products meet quality and safety requirements before reaching customers.

What is the difference between Quality Control Sample Coordinator vs Quality Control Technician?

AspectQuality Control Sample CoordinatorQuality Control Technician
CertificationsOften requires GMP, GLP, or industry-specific certificationsTypically requires GMP or industry-specific certifications
Work EnvironmentCoordinates sample collection and documentation, often in labs or manufacturing facilitiesPerforms testing and analysis directly on samples in laboratory settings
Primary ResponsibilitiesOrganizes sample collection, tracks samples, ensures proper documentationConducts tests, analyzes results, reports findings
Industry UsageCommonly used in pharmaceutical, biotech, and manufacturing industriesCommonly used in pharmaceutical, biotech, and manufacturing industries

The main difference is that the Quality Control Sample Coordinator focuses on sample collection, tracking, and documentation, while the Quality Control Technician performs testing and analysis of samples. Both roles are essential in quality assurance processes within similar work environments and industries.

More about Quality Control Sample Coordinator jobs
What cities are hiring for Quality Control Sample Coordinator jobs? Cities with the most Quality Control Sample Coordinator job openings:
What states have the most Quality Control Sample Coordinator jobs? States with the most job openings for Quality Control Sample Coordinator jobs include:
What job categories do people searching Quality Control Sample Coordinator jobs look for? The top searched job categories for Quality Control Sample Coordinator jobs are:
Infographic showing various Quality Control Sample Coordinator job openings in the United States as of May 2026, with employment types broken down into 98% Full Time, and 2% Contract. Highlights an 47% Physical, 3% Hybrid, and 50% Remote job distribution, with an average salary of $48,903 per year, or $23.5 per hour.

Technician I, QC Sample Management

Bristol Myers Squibb

Devens, MA

$27.35 - $33.14/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago


Job description

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

The QC Sample Management Technician is responsible for the movement and control of QC samples and materials, including in-process, finished drug product, characterization, retain, and stability samples processed through the QC laboratories. This includes, but is not limited to, sample collection and distribution, inventory control, chain of custody, sample tracking, and sample delivery.

This role works from 6AM to 6PM following a 12-hour rotating shift (36/48 hours over a 2-week period) which includes working every other weekend, holidays falling on scheduled workdays, and during adverse weather conditions in support of QC and the manufacturing facility. Flexibility to work irregular hours and short notice overtime may be required.

Education:

Associate's degree in chemistry, Microbiology or related science; or a high school diploma/GED with 2+ years of relevant work experience, preferably in a regulated environment. An equivalent combination of education and experience may substitute.

Experience:

Experience with cold chain sample storage and transfer in a GMP regulated environment is desirable.

Knowledge of basic electronic systems (email, MS Office, etc.).

Experience with LIMS and ELN computer applications preferred.

Able to perform light to moderate lifting and carrying objects up to 20 lbs.

Knowledge of regulatory standards as they apply to GMP laboratories is preferred.

Attention to detail and demonstrated organizational skills.

Ability to adapt and adjust to changing priorities and to manage assignments with challenging/conflicting deadlines.

Ability to work in a high-paced team environment and meet deadlines.

Ability to communicate effectively with peers and department management.

DUTIES AND RESPONSIBILITIES:

Handle test samples throughout the sample lifecycle: receipt, storage, distribution, transfer, and disposal. Facilitate cold chain transfers of samples.

Ensure samples and materials are appropriately labelled and maintain sample tracking, labelling and chain of custody records in accordance with regulatory requirements and written procedures.

Maintain inventory and distribution of QC samples and materials to functional groups as scheduled or requested.

Record performance metrics for the sample management group.

Support identification and implementation of process efficiencies.

Communicate effectively with management regarding task completion, roadblocks, and needs.

WORKING CONDITIONS (US Only):

The incumbent will be working around biohazardous materials and may be exposed to fluctuating and/or extreme temperatures on occasion.

This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position may be required to perform any other job-related duties as requested by management.

Additional Job Requirements:

Position Handles Hazardous Materials

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Compensation Overview:

Devens - MA - US: $27.35 - $33.14per hour

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.

Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:

  • Health Coverage: Medical, pharmacy, dental, and vision care.

  • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).

  • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.

Work-life benefits include:

Paid Time Off

  • US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)

  • Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.

*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1602339 : Technician I, QC Sample Management