ZipRecruiter

Log In

1

Quality Control Associate Jobs in Delaware (NOW HIRING)

WuXi AppTec

QC Microbiology Scientist

Middletown, DE

$24 - $31.50/hr

Mentor and train QC Analysts and Associates on microbiological methods and best practices. * Other QC tasks assigned by microbiology lead. Regulatory Compliance and Documentation * Ensure all ...

WuXi AppTec

QC Microbiology Scientist

Middletown, DE · On-site

$24 - $31.50/hr

Mentor and train QC Analysts and Associates on microbiological methods and best practices. * Other QC tasks assigned by microbiology lead. Regulatory Compliance and Documentation * Ensure all ...

WuXi AppTec

QC Microbiology Scientist

Middletown, DE · On-site

$24 - $31.50/hr

Mentor and train QC Analysts and Associates on microbiological methods and best practices. * Other QC tasks assigned by microbiology lead. Regulatory Compliance and Documentation * Ensure all ...

Qnity

Quality Specialist

Newark, DE · On-site

Associate degree in Engineering, Quality, or a related technical field * Experience: 2-5 years in Quality Assurance or Quality Control within a manufacturing environment * Certifications: Lean and ...

Banfield Pet Hospital

$146K - $219K/yr

If you are a current associate, you will need to apply through our internal career site. Please log into Workday and click on the Jobs Hub app or search for Browse Jobs. Director Veterinary Quality ...

next page

Showing results 1-20

All JobsQuality Control Associate JobsQuality Control Associate Jobs in Delaware

Quality Control Associate information

See Delaware salary details

$11

$25

$38

How much do quality control associate jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for quality control associate in Delaware is $25.48, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $31.06 per hour, depending on experience, location, and employer.

What does a quality control associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

What are the key skills and qualifications needed to thrive as a quality control associate?

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges quality control associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

What is the difference between Quality Control Associate vs Quality Assurance Technician?

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

What are the most commonly searched types of Quality Control jobs in Delaware?

The most popular types of Quality Control jobs in Delaware are:

What cities in Delaware are hiring for Quality Control Associate jobs?

Cities in Delaware with the most Quality Control Associate job openings:

What are popular job titles related to Quality Control Associate jobs in DE?

For Quality Control Associate jobs in DE, the most frequently searched job titles are:

Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Delaware as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $53,008 per year, or $25.5 per hour.

QC Microbiology Scientist

WuXi AppTec

Middletown, DE

$24 - $31.50/hr

Full-time

Posted 14 days ago

Job description

Reporting to the QC Microbiology Lead, the QC Microbiology Scientist will perform advanced microbiological laboratory activities in support of drug product manufacturing at WuXi STA’s Middletown, DE site. This role includes execution and troubleshooting of microbiological testing, environmental monitoring, stability sample handling, equipment operation, method transfers, and documentation in accordance with GMP, corporate quality standards, and regulatory requirements. The QC Microbiology Scientist will support both startup and steady-state operations, ensuring timely and accurate completion of QC tasks for product release, stability studies, validation, and regulatory audits.


Microbiological Testing and Support
  • Perform and review advanced microbiological QC testing for drug products, raw materials, packaging components, and utilities in accordance with approved methods and SOPs.
  • Lead and execute environmental monitoring, bioburden, endotoxin, microbial limits, microbial identification, and sterility testing.
  • Provide scientific expertise in troubleshooting, investigations, and technical issue resolution.
  • Author, review, and revise SOPs, test methods, and technical documents.
  • Mentor and train QC Analysts and Associates on microbiological methods and best practices.
  • Other QC tasks assigned by microbiology lead.
Regulatory Compliance and Documentation
  • Ensure all activities are conducted in strict compliance with cGMP, safety, and quality standards.
  • Maintain accurate, complete, and inspection-ready microbiology laboratory documentation.
  • Participate in method transfer, qualification, and validation of microbiological methods and equipment.
  • Support client and regulatory audits by presenting data, explaining technical approaches, and preparing responses.
  • Escalate deviations, out-of-specification (OOS) results, or atypical findings promptly to the QC Microbiology Manager.

  • Bachelor’s degree in Microbiology, Biology, or related scientific discipline with 5+ years of QC microbiology experience in a GMP-regulated pharmaceutical or biotechnology environment; OR
  • Master’s degree with 3+ years or PhD with 1+ years of relevant QC microbiology experience.
  • Deep expertise in microbiological techniques and instrumentation, including environmental monitoring, sterility, endotoxin, and bioburden testing.
  • Demonstrated ability to lead investigations, author technical reports, and drive resolution of complex issues.
  • Strong knowledge of GMP regulations, USP <61>, <62>, <85>, <1116>, ICH guidelines, and data integrity principles.

Preferred Qualifications

  • Experience with LIMS, Empower, or other electronic laboratory systems.
  • Previous work in a CDMO or multi-client environment.
  • Demonstrated ability to provide technical training and mentorship.
  • Strong communication skills and ability to support audits and regulatory inspections.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against based on disability

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.

Apply