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Quality Control Associate Jobs in Delaware (NOW HIRING)

WuXi AppTec

QC Analytical Scientist

Middletown, DE

Mentor and train QC Analysts and Associates in analytical techniques and best practices. * Other QC tasks assigned by analytical lead. Regulatory Compliance and Documentation * Ensure all activities ...

WuXi AppTec

QC Analyst, Microbial

Middletown, DE · On-site

$22.50 - $30.50/hr

Associate or bachelor's degree in Microbiology, Biology, or related scientific discipline. * 1-3 years of QC microbiology experience in a GMP-regulated pharmaceutical or biotechnology environment ...

WuXi AppTec

QC Analyst, Microbial

Middletown, DE · On-site

$22.50 - $30.50/hr

Associate or bachelor's degree in Microbiology, Biology, or related scientific discipline. * 1-3 years of QC microbiology experience in a GMP-regulated pharmaceutical or biotechnology environment ...

WuXi AppTec

QC Analyst, Microbial

Middletown, DE · On-site

$22.50 - $30.50/hr

Associate or bachelor's degree in Microbiology, Biology, or related scientific discipline. * 1-3 years of QC microbiology experience in a GMP-regulated pharmaceutical or biotechnology environment ...

WuXi AppTec

QC Analytical Scientist

Middletown, DE · On-site

Mentor and train QC Analysts and Associates in analytical techniques and best practices. * Other QC tasks assigned by analytical lead. Regulatory Compliance and Documentation * Ensure all activities ...

WuXi AppTec

QC Analytical Scientist

Middletown, DE · On-site

Mentor and train QC Analysts and Associates in analytical techniques and best practices. * Other QC tasks assigned by analytical lead. Regulatory Compliance and Documentation * Ensure all activities ...

WSFS Bank

Quality Control Specialist I

Wilmington, DE · On-site

$45K - $74K/yr

At WSFS Bank, we empower our Associates to grow their careers, guide our customers to secure their ... The Quality Control Specialist will act as gatekeeper to ensure that the highest quality standards ...

MSD

Senior Technician, Quality Control

Millsboro, DE · On-site

$59K - $93K/yr

A Senior QC Lab Tech must possess thorough knowledge of the underlying principles used in testing ... Associate degree in a science plus 2 years of relevant experience OR * Bachelor's degree in ...

Hologic Inc.

Quality Inspector 2

Newark, DE · On-site

At Hologic, we are seeking a Quality Control Inspector to ensure our products meet the highest ... S./GED) required; an Associate Degree is a plus. Why join Hologic? We are committed to making ...

Hologic

Quality Inspector 2

Newark, DE · On-site

At Hologic, we are seeking a Quality Control Inspector to ensure our products meet the highest ... S./GED) required; an Associate Degree is a plus. Why join Hologic? We are committed to making ...

PPG Industries, Inc.

OEM Quality Manager

Houston, DE · On-site

Lead Quality Control operations, including laboratory management, testing, inspection, calibration ... Associate degree or higher in Quality, Engineering, or a related technical discipline preferred ...

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All JobsQuality Control Associate JobsQuality Control Associate Jobs in Delaware

Quality Control Associate information

See Delaware salary details

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$38

How much do quality control associate jobs pay per hour?

As of Aug 12, 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, 77% Full Time, 16% Part Time, 5% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $53,008 per year, or $25.5 per hour.

QC Analytical Scientist

WuXi AppTec

Middletown, DE

Full-time

Posted 15 days ago

Job description

Reporting to the QC Analytical Lead, the QC Analytical Scientist will serve as a technical expert in analytical chemistry testing and laboratory operations in support of drug product manufacturing at WuXi STA’s Middletown, DE site. This role includes advanced execution and troubleshooting of analytical methods, stability studies, method transfers, and equipment qualification, as well as maintaining compliance with GMP, corporate quality standards, and global regulatory requirements. The QC Analytical Scientist will play a critical role in both startup and steady-state operations, ensuring timely and accurate testing for product release, validation, and regulatory inspections.


QC Analytical Testing and Support
  • Perform and review QC analytical testing for drug products, raw materials, packaging components, and stability samples in accordance with approved methods and SOPs.
  • Execute advanced analytical techniques including HPLC, UPLC, GC, dissolution, UV-Vis, TOC, Karl Fischer, and other relevant compendial and non-compendial methods.
  • Troubleshoot analytical instrumentation and methods, supporting investigations and continuous improvement.
  • Author, review, and revise test methods, SOPs, and technical documents.
  • Mentor and train QC Analysts and Associates in analytical techniques and best practices.
  • Other QC tasks assigned by analytical 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 laboratory documentation.
  • Participate in method transfer, qualification, and validation of analytical 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 Analytical Manager.

  • Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related scientific discipline with 5+ years of QC analytical laboratory experience in a GMP-regulated pharmaceutical or biotechnology environment; OR
  • Master’s degree with 3+ years or PhD with 1+ years of relevant QC analytical laboratory experience.
  • Deep expertise in chromatographic and spectroscopic methods (HPLC/UPLC, GC, UV-Vis, TOC, KF, etc.) and data interpretation.
  • Demonstrated ability to lead laboratory investigations, troubleshoot instrumentation, and author technical reports.
  • Strong knowledge of GMP regulations, ICH guidelines, and data integrity principles (ALCOA+).

Preferred Qualifications

  • Experience in method transfer, qualification, and validation of analytical methods.
  • Familiarity with LIMS, Empower, or other electronic laboratory management systems.
  • Prior experience in a CDMO or multi-client environment.
  • Strong communication and collaboration skills to support cross-functional teams, 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.

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