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Quality Control Sample Coordinator Jobs in Edison, NJ

Glanbia

QUALITY CONTROL TECHNICIAN

Linden, NJ · On-site

$19.25 - $24.75/hr

Quality Control Related Responsibilities * Implement various analytical tests on incoming samples ... Logging samples into the Sample Data Base. * Performing analytical tests using the following ...

Union Beverage

Quality Control Batcher

Hillside, NJ

$17.25 - $21/hr

Perform quality checks as required. * Control flow of syrup to production lines. * Set equipment ... Pull water samples from mixing and syrup tanks for tasting * Follow GMP's and Food Safety ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and Manufacturing to meet production timelines Requirements * 6-8+ years of pharmaceutical QC experience (cGMP ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and Manufacturing to meet production timelines Requirements * 6-8+ years of pharmaceutical QC experience (cGMP ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and Manufacturing to meet production timelines Requirements * 6-8+ years of pharmaceutical QC experience (cGMP ...

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All JobsQuality Control Sample JobsQuality Control Sample Coordinator JobsQuality Control Sample Coordinator Jobs in Edison, NJ

Quality Control Sample Coordinator information

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$24

$34

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

As of Sep 2, 2026, the average hourly pay for quality control sample coordinator in Edison, NJ is $24.34, according to ZipRecruiter salary data. Most workers in this role earn between $19.66 and $27.12 per hour, depending on experience, location, and employer.

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 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 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.

What are popular job titles related to Quality Control Sample Coordinator jobs in Edison, NJ?

For Quality Control Sample Coordinator jobs in Edison, NJ, the most frequently searched job titles are:

What job categories do people searching Quality Control Sample Coordinator jobs in Edison, NJ look for?

The top searched job categories for Quality Control Sample Coordinator jobs in Edison, NJ are:

What cities near Edison, NJ are hiring for Quality Control Sample Coordinator jobs?

Cities near Edison, NJ with the most Quality Control Sample Coordinator job openings:

Quality Control Sample Coordinator jobs near you
Infographic showing various Quality Control Sample Coordinator job openings in Edison, NJ as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 5% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $50,627 per year, or $24.3 per hour.

QUALITY CONTROL TECHNICIAN

Glanbia

Linden, NJ • On-site

$19.25 - $24.75/hr

Full-time

Re-posted yesterday

Glanbia Performance Nutrition rating

8.6

Company rating: 8.6 out of 10

Based on 38 frontline employees who took The Breakroom Quiz

29th of 443 rated food and drinks producers

Job description

Quality Control Related Responsibilities
  • Implement various analytical tests on incoming samples of raw materials (RM), product components (Intermediates), and Finished Products to assure the Quality of the component. These include but are not limited to:
    • Logging samples into the Sample Data Base.
    • Performing analytical tests using the following testing equipment and recording results:
      • Densitometer (SG-Specific Gravity)
      • Refractometer (RI-Refractive Index)
      • VIS-Spectrophotometer (ABS-Color Absorbance)
      • pH meter
      • GC FID
      • Alcohol by Distillation
  • QC testing and data review, CoA generation.
    • Compare test results with specification ranges to determine batch to batch consistency of the product.
  • Maintain Customer Specifications in ERP system and Batch Works systems to ensure consistent communication of specifications to customers and equivalence of the two specification management systems.
  • Support Research and Development by providing analytical support for all requested sampling.
  • Product approval in ERP / warehouse
  • Coordinate with production/operations to document production yields.
  • Communicate issues to Quality and/or Production Management, take ownership of solving batch-specific problems
  • Assist in complaint investigation and data gathering.
  • Coordinate and perform, with trained team all sensory analysis of incoming samples according to established procedures.
  • Shelf life extension evaluations for finished products, and raw material / intermediate expiration evaluations.
  • Organization and cataloguing of retain library, samples folders, paperwork organization, ordering retains to support QC evaluation.
  • Maintain cleanliness of the lab according to Good Laboratory Practices.
  • Order supplies and reagents.
  • Create transmittals and associated sample request forms and labels for outside testing, gather / prepare these for shipment.
  • Retrieve and send documents related to Internal RM / Intermediate transfers and for Regulatory requests.
  • Update and communication raw material, intermediate, and finished product specifications as required
  • Respond and provide formula information to support regulatory requests
  • Ensure effective communication of all quality related information with other departments.

Competencies
To perform the job successfully, an individual should demonstrate the following competencies:
Optimizes Work Process- Knowing the most effective and efficient processes to get things done, with a focus on continuous improvement.
Collaborates- Building partnerships and working collaboratively with others to meet shared objectives.
Self-Development- Actively seeking new ways to grow and be challenged using both formal and informal development channels.
Communicates Effectively- Developing and delivering multi-mode communications that convey a clear understanding of the unique needs of different audiences.
Analytical - synthesizes complex or diverse information; collects and researches data; uses intuition and experience to complement data; designs workflows and procedures.
Teamwork - balances team and individual responsibilities; exhibits objectivity and openness to others' views; gives and welcomes feedback; contributes to building a positive team spirit; puts success of team above own interests; able to build morale and group commitments to goals and objectives; supports everyone's efforts to succeed.
Safety and security - observes safety and security procedures; determines appropriate action beyond guidelines; reports potentially unsafe conditions; uses equipment and materials properly.
Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
Successful completion of a 4-year degree in chemistry, biology, microbiology, food science, or related field
Experience in QC Laboratory setting for 1-3 years, ideally in Flavor or Food industry.
Experience maintaining and troubleshooting lab instrumentation, such as spectrophotometers and gas chromatography.
Experience with performance of organoleptic testing and release of product against quality standards
At Glanbia, we celebrate diversity, because we know that our individual strengths make us stronger together. We welcome and encourage interest from a wide variety of candidates, and we will give your application consideration, without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status.
At Glanbia our culture will celebrate individuality, knowing that together we are more.

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