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Quality Control Manager Jobs in Thorofare, NJ (NOW HIRING)

The QC Manager manages laboratory personnel, oversees testing operations, ensures timely release of analytical data, supports investigations, and drives continuous improvement initiatives while ...

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QC Technician

Boothwyn, PA · On-site

$18 - $23/hr

QC Technician (2 Needed)The position is 8;00am â€" 4:30pm daily Monday â€" Friday. ½ hr ... Interaction with all plant / warehouse staff• Reports to Dennis and Bob (plant manager ...

Quality Control Technician

Bridgeport, NJ

$17.75 - $23/hr

The Technician I, FSQA-Bakery conducts food safety and quality assurance procedures to ensure J&J ... manage and execute changes. Position requires ability to act as a member of a highly functioning ...

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Quality Control Manager information

See Thorofare, NJ salary details

$29.7K

$79.2K

$126.1K

How much do quality control manager jobs pay per year?

As of Aug 22, 2026, the average yearly pay for quality control manager in Thorofare, NJ is $79,192.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,900.00 and $97,400.00 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 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 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 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.

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.

Is a Quality Control Manager a high paying job?

A Quality Control Manager typically earns a salary above the national average for managerial roles, with pay varying based on industry, experience, and location. They often require skills in inspection, testing, and quality assurance, and may hold certifications such as Six Sigma or ISO auditor training. Overall, it is considered a well-compensated position within manufacturing, production, and related sectors.

What is the work of a quality control manager?

A quality control manager oversees the inspection and testing of products or services to ensure they meet quality standards and specifications. They develop quality control procedures, analyze data, and coordinate with production teams to address issues, often using tools like inspection equipment and quality management systems. The role requires attention to detail, problem-solving skills, and knowledge of industry regulations.

What job categories do people searching Quality Control Manager jobs in Thorofare, NJ look for?

The top searched job categories for Quality Control Manager jobs in Thorofare, NJ are:

What cities near Thorofare, NJ are hiring for Quality Control Manager jobs?

Cities near Thorofare, NJ with the most Quality Control Manager job openings:

Infographic showing various Quality Control Manager job openings in Thorofare, NJ as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $79,192 per year, or $38.1 per hour.

Quality Control Manager

Epicur

Mount Laurel, NJ • On-site

$75K/yr

Full-time

Posted 3 days ago

New


Job description

Summary/Objective

The Quality Control (QC) Manager is responsible for overseeing all Quality Control operations and in-process quality activities associated with the manufacturing of drug products at Epicur Pharma. This position requires experience and knowledge in manufacturing, microbiology, and analytic chemistry; additionally, operating requirements in accordance with cGMP (21 CFR Part 210 and 211). This role ensures testing activities are performed in compliance with current Good Manufacturing Practices (cGMP), FDA regulations, USP standards, and company quality systems. The QC Manager manages laboratory personnel, oversees testing operations, ensures timely release of analytical data, supports investigations, and drives continuous improvement initiatives while maintaining the highest standards of product quality and regulatory compliance.


Salary


$75K based on experience plus twice a year bonuses.

Essential Duties and Responsibilities include the following. Other duties may be assigned.

  • Familiar with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP)
  • Leads, mentors, and develops employees within Quality Control Department.
  • Dispositions and approves quality testing/inspection of incoming components, raw materials, finished product, and stability sample.
  • Leads development of sampling protocols for in-process materials and finished products.
  • Oversee the testing of raw materials, Active Pharmaceutical Ingredients (APIs), Components, In-process samples and Finished products.
  • Manage the visual inspection program.
  • Assist in review and disposition of root cause analysis, risk assessments, and investigation involving manufacturing and quality operations.
  • Monitor KPIs and identifies CAPA for quality functions.
  • Conduct and review internal audits of processes, systems, and procedures.
  • Provide leadership across functional groups to resolve issues relating to product or production quality.
  • Oversight of method validations for chemistry and microbiology testing methods.
  • Participation in deviation reports, investigations, and CAPA.
  • Participates in Annual Product Reviews providing Quality related data and trend reports.
  • QC review of executed batch record and release of finished drug products.
  • Research current Quality/Regulatory requirements, as applicable, and leads SOP implementation/revision to assure compliance and continuous improvement of the overall operation.
  • Ensure all Quality related documents generated at the facility are received by document control at the appropriate time per procedure.
  • Oversees programs are established maintained for respirator fit test and respirator use protocols to ensure safety of employees and conformance with OSHA and NIOSH regulations.

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Required Education and Experience

  • Bachelor’s degree in Biology, Microbiology, Biochemistry, Biotechnology or Chemistry
  • 3+ years of experience directly managing employees including; hiring, performance management, scheduling and conflict resolution required
  • 3-5 years of experience in years of experience in the pharmaceutical industry in drug substance or drug product manufacturing in Quality Control or Quality Assurance
  • Workplace Safety experience a plus  Strong organizational, problem solving, analytical, and management skills Familiar with GxP, FDA, ICH, and OSHA requirements
  • Familiar with Microsoft Office applications (Word, Excel, etc.)  Must be capable of wearing all protective wear as required. This includes, but not limited to, mask, gloves, gown, hairnet, safety goggles, etc.
  • Must have strong organizational skills and exceptional attention to detail
  • Must exhibit punctuality and low absenteeism
  • Able to work independently and as part of a team
  • Able to sit, stand, squat, kneel, reach and walk for prolonged periods of time
  • May need to lift up to twenty-five (25) pounds on occasion

Competencies

  • Communication Proficiency
  • Decision Making
  • Detail Oriented
  • Leadership Skills
  • cGMP Manufacturing
  • Problem Solving/Analysis
  • Project Management
  • Results Driven
  • Technical Capacity
  • Innovation

Supervisory Responsibility

This position has supervisory responsibilities for the Quality Control Department


Work Environment

This job operates in both office/shared, controlled manufacturing environments and laboratory testing environments. This position requires the use of standard office equipment, and frequent standing and walking.

Language Skills

Must be able to read, write, speak and understand English fluently and have the ability to read and interpret documents such as operating and maintenance instructions and procedure manuals.

Mathematical Skills

Uses addition, subtraction, multiplication and the division of numbers including decimals and fractions when checking of reports, forms, records and comparable data where interpretation is required involving basic skills knowledge.

Reasoning Ability

Must have the ability to solve practical problems and deal with a variety of concrete variables in situations where substantial standardization exists. Must be able to interpret instructions furnished in written, oral, and diagram or schedule form.

Physical Demands

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

  • Able to sit and/or stand 8-10 hours or more per day as needed
  • May sit, stand, stoop, bend and walk intermittently during the day; may be necessary to work extended hours as needed
  • Finger dexterity to operate office equipment required
  • Ability to lift up to twenty-five (25) pounds on occasion

Position Type and Expected Hours of Work

This is a full-time position. Because of the nature of the business, work schedules may vary at times.

Travel

No travel is expected for this position.


Disclaimer

The above job description is intended to describe the general nature and level of work being performed by employees assigned to this job. It is not designed to capture or illustrate a comprehensive list of all responsibilities, duties, and skills required of employees assigned to this job.

AAP/EEO Statement

Stokes Healthcare is an Equal Employment Opportunity and Affirmative Action Employer.