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Quality Control Manager Jobs in Chester, PA (NOW HIRING)

Frontage Laboratories

QC Manager

Exton, PA · On-site

QC Manager - Biomarker and Biologics Laboratory Job Title: Quality Control (QC) Manager Department: Biomarker & Biologics Location: Exton, PA ( Onsite) Position Summary The QC Manager is responsible ...

Mintex Technology

Quality Control Manager

West Chester, PA · On-site

$32.75 - $48/hr

Quality Control Manager Location: West Chester, Pennsylvania - 100% Onsite Shift : 1st Shift Salary : $80,000 - $100,000/year OR $32.75 - $48.00/hour Type: Fulltime with full benefits About: Our ...

Actalent

Traveling QC Manager

West Chester, PA

$45 - $68/hr

Traveling Quality Control Manager We are seeking a Quality Control Manager to oversee a large-scale environmental remediation project. This Superfund cleanup project involves addressing historical ...

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All JobsQuality Control JobsQuality Control Manager JobsQuality Control Manager Jobs in Chester, PA

Quality Control Manager information

See Chester, PA salary details

$29.4K

$78.5K

$124.9K

How much do quality control manager jobs pay per year?

As of Aug 7, 2026, the average yearly pay for quality control manager in Chester, PA is $78,450.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,400.00 and $96,500.00 per year, depending on experience, location, and employer.

What does a quality control manager do?

A Quality Control Manager is responsible for overseeing and ensuring the quality of products or services within an organization. They develop and implement quality control procedures, inspect products, and monitor operations to ensure compliance with industry standards and regulations. Additionally, they analyze quality data, identify areas for improvement, and work closely with other departments to resolve quality issues. Their goal is to maintain high standards and minimize defects or errors in the final output.

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

AspectQuality Control ManagerQuality Assurance Supervisor
Primary FocusInspecting products and processes to identify defectsDeveloping and implementing quality systems and procedures
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, production lines, labsQuality departments, process improvement teams
Employer UsageManufacturers, factories, production facilitiesCompanies with formal quality management systems

Both roles focus on quality but differ in scope. The Quality Control Manager primarily inspects products to catch defects, while the Quality Assurance Supervisor develops systems to prevent defects. Understanding these differences helps in choosing the right career path or hiring focus.

What are the biggest challenges a quality control manager typically faces when implementing new quality standards?

One of the main challenges Quality Control Managers encounter is ensuring that all team members understand and consistently adhere to newly implemented quality standards. This often involves extensive training, clear documentation, and continuous monitoring to address resistance to change or misunderstandings. Additionally, balancing the need for thorough quality checks with production deadlines can be demanding, requiring strong communication and problem-solving skills to align quality goals with operational efficiency. Collaborative efforts with production, engineering, and compliance teams are essential to successfully integrate new standards while maintaining workflow.

What does a quality control manager do?

As a quality control manager, your responsibilities are to ensure that your company’s products are up to industry standards by inspecting items and overseeing the efficiency of production and manufacturing processes. Your job duties as a quality control manager include coordinating between company management and production departments, implementing strategies to maximize employee efforts, and evaluating processes on manufacturing and production lines. Your focus is on quality assurance of both processes and output to minimize the number of problems that inspectors might identify when visiting the company.

What are the key skills and qualifications needed to thrive as a quality control manager, and why are they important?

To thrive as a Quality Control Manager, you need expertise in quality assurance processes, analytical skills, and a background in science or engineering, often supported by a relevant degree. Familiarity with quality management systems (such as ISO 9001), statistical analysis software, and internal auditing tools is typically required. Strong leadership, problem-solving abilities, and excellent communication help drive team performance and foster a culture of continuous improvement. These skills ensure that products meet strict standards, reduce defects, and maintain customer satisfaction in a competitive market.
More about Quality Control Manager jobs
What job categories do people searching Quality Control Manager jobs in Chester, PA look for? The top searched job categories for Quality Control Manager jobs in Chester, PA are:
What cities near Chester, PA are hiring for Quality Control Manager jobs? Cities near Chester, PA with the most Quality Control Manager job openings:
Quality Control Manager jobs near you
Infographic showing various Quality Control Manager job openings in Chester, PA as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 18% Part Time, 5% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $78,450 per year, or $37.7 per hour.

QC Manager

Frontage Laboratories

Exton, PA • On-site

Full-time

Re-posted 25 days ago

Job description

Job Description: QC Manager – Biomarker and Biologics Laboratory

Job Title: Quality Control (QC) Manager
Department: Biomarker & Biologics
Location: Exton, PA (Onsite)

Position Summary

The QC Manager is responsible for oversight of the Quality Control function supporting compliant biologics and biomarker testing performed using ligand-binding assay (LBA) platforms and other immunoassay. This role ensures that study data, assay performance, regulated documentation, and reporting meet GLP, data integrity, and client requirements. The QC Manager leads a team of QC reviewers responsible for data verification, review of assay outputs, documentation accuracy, and compliance across all GLP bioanalytical studies.

Key Responsibilities

Oversight for Bioanalytical LBA Studies

  • Ensure QC activities adhere to GLP regulations (FDA 21 CFR Part 58, OECD GLP) and bioanalytical industry expectations (FDA/EMA BMV guidance).
  • Assign QC reviewer to the studies and maintain QC review capacity to ensure timely delivery of QC’ed data/reports/deliverable with high quality.
  • Oversee QC review of study data and study integrity. Provide guidance and training to QC team to establish/optimize sustainable review process and improve the effectiveness and accuracy of QC review.

Data Review & Study Support

  • Lead QC review of validation protocols, sample analysis plans, plate layouts, run sheets, and controlled forms.
  • Ensure GLP sample analysis is performed according to validated methods, study protocols, and SOPs.
  • Confirm integrity of electronic data (ELN/LIMS, plate reader software, instruments outputs).
  • Review bioanalytical reports, validation summaries, run acceptance decisions, and performance qualification documentation.
  • Collaborate with PI/RS, Bioanalytical Scientists, and QA to address errors, deviations.
  • Support on the data and documentation review for the CAP/CLIA assays handled by biomarker and biologics team.

Management

  • Lead, train, and mentor QC reviewers and specialists supporting the workflows.
  • Allocate workloads to meet numerous parallel GLP validation and sample-analysis timelines.
  • Maintain a highly organized QC workflow to support fast-turnaround studies and late-stage clinical sample testing.
  • Build competency in reviewing complex LBA datasets, including multiplex assays, bridging assays, ADA/NAb workflows, biomarker assays and pharmacokinetics (PK) immunoassays.

Quality Systems & Documentation

  • Oversee controlled documents including QC training documentation, controlled forms, templates, QC checklists and relevant QC documents.
  • Support and review deviations, investigations and reports/reports templates.
  • Ensure reviewed study documents meeting the GLP compliance and follows SOPs.

Continuous Improvement & Laboratory Support

  • Establish QC metrics (review cycle time, error rates, audit observations) and drive continuous process improvements.
  • Provide feedback on process gaps, such as data integrity gaps in LIMS or instrument workflows (e.g., SoftMax Pro, MSD Discovery Workbench, SIMOA software).
  • Implement improvements in plate-level documentation, run acceptance criteria, and audit trails.
  • Support inspection readiness for FDA, EMA, and client audits.
  • Drive harmonization and standardization of QC workflows across LBA platforms.

Qualifications

Education

  • Bachelor’s or Master’s in Biology, Biochemistry, Immunology, Biotechnology, or related field.

Experience

  • 5–10+ years of experience in regulated bioanalytical laboratories.
  • Strong background in GLP compliance and regulated bioanalysis.
  • Minimum 2–5 years of supervisory or leadership experience in QC, QA, or bioanalytical data review roles.

Skills & Competencies

  • Strong understanding of GLP and FDA/EMA bioanalytical method validation (BMV) guidance.
  • Expertise in immunoassay data review: plate performance, curve fitting models, QC trends, and analytical run acceptance.
  • Proficiency with relevant software (SoftMax Pro, E-WorkBook, Watson LIMS, ELN/LIMS systems).
  • Strong communication skills for interactions with Study Directors, analysts, QA, and clients.
  • Excellent attention to detail and the ability to identify subtle data inconsistencies.
  • Ability to manage multiple concurrent GLP studies under tight deadlines.

Key Personal Attributes

  • High integrity, strong quality mindset, and firm understanding of regulatory expectations.
  • Calm, thorough, and effective in fast-paced study timelines and audit environments.
  • Collaborative, supportive leadership style with a focus on training and developing reviewers.
  • Strong problem-solving approach with focus on risk mitigation and process excellence.