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Manager Qc Jobs in Delaware (NOW HIRING)

WuXi AppTec

QC Raw Material Scientist

Middletown, DE · On-site

The QC Raw Material Scientist will support material disposition, supplier qualification ... Support qualification and lifecycle management of laboratory instruments and computerized systems.

WuXi AppTec

QC Raw Material Scientist

Middletown, DE · On-site

Overview Reporting to the QC Analytical Lead, the QC Raw Material Scientist will serve as a ... Support qualification and lifecycle management of laboratory instruments and computerized systems.

Care Career

Local Contract Quality Control Technician

Lewes, DE · On-site

$18.75 - $23.75/hr

Quality Control Technician * Discipline: Allied Health Professional * Duration: 13 weeks * 40 hours ... Quality Management / Patient Safety 🕐 Shift: 8H Days 📅 Contract: 26 Weeks ⏰ Guaranteed: 40 ...

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Manager Qc information

See Delaware salary details

$24K

$86.2K

$158.1K

How much do manager qc jobs pay per year?

As of Sep 7, 2026, the average yearly pay for manager qc in Delaware is $86,234.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $136,100.00 per year, depending on experience, location, and employer.

What are the responsibilities of a Manager QC?

A Manager QC (Quality Control Manager) is responsible for overseeing the quality assurance processes within a company to ensure that products meet required standards and specifications. They develop and implement quality control procedures, supervise QC staff, conduct audits, and analyze quality data to identify areas for improvement. Additionally, they collaborate with other departments to resolve quality issues and ensure compliance with industry regulations. Their ultimate goal is to maintain consistent product quality and customer satisfaction.

What skills and qualifications are needed to thrive as a Manager QC?

To thrive as a Manager QC (Quality Control), you need a solid background in quality assurance processes, analytical testing, and industry regulations, typically supported by a degree in science or engineering. Familiarity with quality management systems (like ISO standards), statistical analysis software, and certification such as Six Sigma or ASQ is often required. Strong leadership, problem-solving, and communication skills help drive team performance and handle complex quality issues. These skills are essential for maintaining product standards, ensuring regulatory compliance, and supporting continuous improvement within the organization.

What challenges does a Manager QC face when balancing regulatory compliance with production timelines?

A Manager QC (Quality Control) often faces the challenge of ensuring that all products meet strict regulatory standards while also supporting the company's production goals. This balancing act requires effective communication with production and regulatory teams, as well as proactive planning to anticipate potential bottlenecks. Managers must remain vigilant about documentation and testing, and be prepared to address unforeseen quality issues without causing significant delays. Success hinges on strong leadership, a detail-oriented mindset, and the ability to adapt quickly to changing priorities.

What is the difference between Manager Qc vs Quality Assurance Supervisor?

AspectManager QcQuality Assurance Supervisor
ResponsibilitiesOversees quality control processes, manages teams, implements quality policiesSupervises QA team, conducts inspections, ensures compliance with standards
CredentialsBachelor's degree in related field, experience in quality management, certifications like CQEBachelor's degree, experience in quality assurance, certifications like CQE or ASQ certifications
Work EnvironmentManagement level, strategic planning, cross-department collaborationOperational level, hands-on inspections, team supervision
Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, electronics, consumer goods

The main difference between a Manager Qc and a Quality Assurance Supervisor lies in scope and level of responsibility. The Manager Qc typically handles strategic oversight and manages multiple teams, while the QA Supervisor focuses on daily supervision and operational tasks. Both roles require similar credentials and are vital in quality management across industries.

Is manager QC a high paying job?

Manager QC roles typically offer higher salaries compared to entry-level quality control positions, with pay varying based on industry, experience, and location. These roles often require strong leadership, technical skills, and certifications, and they tend to be well-compensated in manufacturing, pharmaceuticals, and food industries.

What does a manager QC do?

A manager QC (Quality Control) oversees the inspection and testing of products or processes to ensure they meet quality standards. They develop quality procedures, supervise QC staff, analyze data, and implement improvements to maintain product integrity and compliance with industry regulations.

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

The most popular types of Qc jobs in Delaware are:

Manager Qc jobs near you
Infographic showing various Manager Qc job openings in Delaware as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $86,234 per year, or $41.5 per hour.

QC Raw Material Scientist

WuXi AppTec

Middletown, DE • On-site

Other

Re-posted 7 days ago

Job description

Reporting to the QC Analytical Lead, the QC Raw Material Scientist will serve as a technical expert in analytical chemistry testing and laboratory operations supporting the release of raw materials, excipients, active pharmaceutical ingredients (APIs), process materials, and packaging components used in pharmaceutical manufacturing at WuXi STA’s Middletown, DE site.  This role is responsible for the execution, troubleshooting, transfer, and validation of analytical methods used for incoming material testing while ensuring compliance with cGMP requirements, compendial standards, corporate quality systems, and global regulatory expectations. The QC Raw Material Scientist will support material disposition, supplier qualification, investigations, and regulatory inspections to ensure an uninterrupted supply of qualified materials for manufacturing operations.

QC Raw Material Testing and Support
  • Perform and review QC analytical testing of raw materials, APIs, excipients, and packaging components according to approved specifications, pharmacopeial methods, and SOPs.
  • Execute compendial and non-compendial analytical methods including HPLC, UPLC, GC, FTIR, UV-Vis, TOC, Karl Fischer, wet chemistry, identification testing, and other applicable techniques.
  • Perform raw material identity testing in accordance with regulatory requirements and internal procedures.
  • Support sampling plans and testing strategies for incoming materials.
  • Conduct laboratory investigations associated with out-of-specification (OOS), out-of-trend (OOT), atypical results, and laboratory deviations related to raw materials.
  • Troubleshoot analytical instrumentation and methods and implement scientifically sound corrective actions.
  • Support supplier qualification and material assessments through analytical evaluation and trending of test results.
  • Author, review, and revise raw material specifications, test methods, protocols, SOPs, and technical reports.
  • Mentor and train QC Analysts on raw material testing techniques, GMP requirements, and laboratory best practices.
  • Collaborate with Warehouse, Manufacturing, Procurement, Quality Assurance, and Supply Chain teams to ensure timely disposition of incoming materials.
  • Support establishment of raw material testing capabilities during site startup and commercial operations.
Regulatory Compliance and Documentation
  • Ensure all laboratory activities are conducted in compliance with cGMP regulations, data integrity principles (ALCOA+), safety requirements, and company quality systems.
  • Maintain complete, accurate, and inspection-ready laboratory records.
  • Support qualification, validation, verification, and transfer of analytical methods used for raw material testing.
  • Support qualification and lifecycle management of laboratory instruments and computerized systems.
  • Review analytical data and approve test results for material release decisions.
  • Participate in audits and regulatory inspections and provide technical responses related to raw material testing programs.
  • Escalate quality events, OOS results, supplier-related concerns, and compliance issues to QC management in a timely manner.
  • Support continuous improvement initiatives to enhance laboratory efficiency, compliance, and turnaround times.
  • 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.
  • Strong experience with raw material release testing, compendial testing, and material disposition processes
  • Demonstrated expertise in chromatographic, spectroscopic, and wet chemistry techniques including HPLC/UPLC, GC, FTIR, UV-Vis, TOC, Karl Fischer, and pharmacopeial analytical methods.
  • Experience leading laboratory investigations, troubleshoot instrumentation, and author technical reports.
  • Strong understanding of USP, EP, JP, ICH, FDA, and cGMP requirements applicable to raw material testing.
  • Strong technical writing skills with experience authoring specifications, SOPs, protocols, and investigation reports.

Preferred Qualifications

  • Experience supporting raw material programs in pharmaceutical manufacturing, or CDMO environments.
  • Experience with supplier qualification, vendor change assessments, and material risk evaluations.
  • Experience performing FTIR identity testing and compendial verification activities.
  • Familiarity with LIMS, Empower, SAP, or similar laboratory and ERP systems.
  • Experience with method transfers, validation, and regulatory inspections.
  • Strong communication and cross-functional collaboration skills supporting Quality Assurance, Supply Chain, Manufacturing, and external suppliers.

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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