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Quality Control Jobs in Flanders, NJ (NOW HIRING)

This position will work with the Quality Control team in supporting our efforts in the GMP manufacturing of cellular therapy products. This individual will lead a group of QC analysts performing ...

This position will work with the Quality Control team in supporting our efforts in the GMP manufacturing of cellular therapy products. This individual will lead a group of QC analysts performing ...

Manager, Quality Control

Bridgewater, NJ · On-site

$90K - $210K/yr

This position will work with the Quality Control team in supporting our efforts in the GMP manufacturing of cellular therapy products. This individual will lead a group of QC analysts performing ...

We are seeking an innovative, creative, and detail-oriented Quality Control Analyst to join our team in Bridgewater, New Jersey. This position will be responsible for routine and non-routine QC ...

We are seeking an innovative, creative, and detail-oriented Quality Control Analyst to join our team in Bridgewater, New Jersey. This position will be responsible for routine and non-routine QC ...

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

We are seeking an innovative, creative, and detail-oriented Quality Control Analyst to join our team in Bridgewater, New Jersey. This position will be responsible for routine and non-routine QC ...

Quality Control Inspector

Butler, NJ · On-site

$22 - $25/hr

Job Title : Quality Control Inspector Location : Butler, New Jersey Type : Contract-to-Hire Compensation : $22-$25/hour plus shift differential (depending on experience) Contractor Work Model

Quality Control Line Inspector Location: Wharton, NJ Employment Type: Direct Hire Shifts Available: * 1st Shift (7:00 AM to 3:00 PM): $21.00/hour * 2nd Shift (3:00 PM to 11:00 PM): $23.00/hour * 3rd ...

Quality Control Inspector

Peapack, NJ · On-site

$70K - $83K/yr

The Quality Control Inspector is responsible for performing incoming, in-process, and final inspections to ensure materials, components, and finished equipment meet engineering drawings, customer ...

Quality Control Line Inspector Location: Wharton, NJ Employment Type: Direct Hire Shifts Available: * 1st Shift (7:00 AM to 3:00 PM): $21.00/hour * 2nd Shift (3:00 PM to 11:00 PM): $23.00/hour * 3rd ...

QC Coordinator

Wayne, NJ · On-site

$32 - $35/hr

Verify that all QC, inspection, testing, checklist and documentation requirements have been completed and properly recorded * Ensure GDP (Good Documentation Practices) compliance, including review of ...

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Quality Control information

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How much do quality control jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for quality control in Flanders, NJ is $22.04, according to ZipRecruiter salary data. Most workers in this role earn between $17.74 and $24.66 per hour, depending on experience, location, and employer.

What is the job of quality control?

The job of quality control involves inspecting products or services to ensure they meet specified standards and are free of defects. Quality control professionals use testing, measurements, and documentation to identify issues and improve processes, often working with tools like checklists and quality management systems. Strong attention to detail and knowledge of industry standards are essential for this role.

What is the difference between Quality Control vs Quality Assurance?

AspectQuality ControlQuality Assurance
FocusDetecting defects in products or servicesPreventing defects through process improvements
ActivitiesInspections, testing, samplingProcess audits, standards development
CredentialsOften requires technical training or certifications in testingCertifications like ISO, Six Sigma are common
Work EnvironmentLaboratory, production lines, manufacturingProcess development, documentation, audits

While Quality Control focuses on identifying defects after production, Quality Assurance aims to prevent defects through process improvements. Both roles are essential for maintaining product quality, but they differ in approach and activities.

Do you need a degree for quality control?

A degree is not always required for a quality control position, as many employers accept candidates with a high school diploma or equivalent. However, having post-secondary education or certifications in quality management, such as Six Sigma or ISO standards, can improve job prospects and advancement opportunities.

Is quality control a good career choice?

Quality control is a viable career that involves inspecting products and processes to ensure standards are met, often requiring attention to detail and knowledge of industry regulations. It can offer stable employment with opportunities for advancement and may require certifications or training in specific tools or standards. The field is important across many industries, including manufacturing, healthcare, and food production.

What is quality control?

Quality control (QC) is a process by which businesses ensure that their products or services meet specific standards of quality. This typically involves systematic inspection, testing, and corrective actions to detect and address defects or inconsistencies. Quality control helps maintain customer satisfaction, comply with regulations, and reduce waste or costly errors. QC can be applied at various stages of production and is essential in industries such as manufacturing, food production, and pharmaceuticals.

What are some common challenges faced by quality control professionals and how can they be addressed?

Quality Control professionals often encounter challenges such as maintaining consistency across production batches, adapting to new regulatory standards, and managing tight deadlines without compromising quality. Addressing these challenges requires strong attention to detail, effective communication with production and engineering teams, and continuous learning to stay updated on industry best practices. Many companies support their QC staff with regular training sessions, clear documentation protocols, and collaborative problem-solving meetings to ensure quality standards are upheld.

Is quality control a good career path?

Quality control is a viable career that involves inspecting products and processes to ensure standards are met, often requiring attention to detail and knowledge of industry regulations. It can lead to advancement into supervisory or specialized roles and may require certifications such as Six Sigma or ISO standards. The job typically offers stable employment in manufacturing, healthcare, or technology sectors.

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

To thrive as a Quality Control professional, you need keen attention to detail, analytical skills, and a background in science, engineering, or manufacturing, often supported by relevant certifications like Six Sigma or ISO standards. Familiarity with quality management systems (QMS), statistical process control (SPC) software, and inspection equipment is typically required. Strong problem-solving abilities, communication, and teamwork set top performers apart in this role. These skills are crucial to ensure product consistency, prevent defects, and maintain compliance with industry standards.
What cities near Flanders, NJ are hiring for Quality Control jobs? Cities near Flanders, NJ with the most Quality Control job openings:
Infographic showing various Quality Control job openings in Flanders, NJ as of August 2026, with employment types broken down into 88% Full Time, 6% Contract, and 6% Nights. Highlights an 100% In-person job distribution, with an average salary of $45,839 per year, or $22 per hour.

Manager, Quality Control

Cellares

Bridgewater, NJ

$90K - $210K/yr

Full-time

Re-posted 24 days ago


Job description

We are seeking an innovative and highly motivated individual to join our team as the Manager of Quality Control at our GMP manufacturing facility located in Bridgewater, NJ. This position will work with the Quality Control team in supporting our efforts in the GMP manufacturing of cellular therapy products.

This individual will lead a group of QC analysts performing analytical testing of in-process and final product from cell therapy products.  They will interface across different parts of the company to support novel products used in cell and gene therapy. This role will report to the Senior Director of Quality Control.

Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. 

Responsibilities
  • Schedule/Manage routine and non-routine analysis of in-process, finished goods, or stability samples
  • Ensure the quality control lab is held to GxP standards and safety standards
  • Create/Review and approve Certificate of Analysis
  • Conduct investigation regarding out of specifications (OOS) results and address and manage deviations related to analytical procedures
  • Review and approve data to ensure accuracy and regulatory compliance
  • Create/Review and approve new and revision of analytical test methods
  • Create/Review and approve method validation protocols/reports and other documentation such as analytical reports
  • Create/Review and approve stability protocols and reports
  • Create/Review and approve quality control operation procedures
  • Manage the validation of analytical methods used in QC as well as the transfer and validation of methods to contract testing laboratories
  • Manage training of other analysts to perform laboratory procedures and assays
  • Participate in internal assessments and audits as required
  • Manage stability program
  • Serve as Quality Control representative during cross-functional/project meetings
  • Serve as subject matter expert between Quality Control and other departments, vendors, or contractors
  • Support Quality Systems such as Change Control, Deviation, CAPA, Audits, Quality Metrics
  • Manage and grow a phase appropriate team of Quality Control personnel
  • Establish user requirements for purchase of new Cellares GMP lab equipment
  • Manage equipment validation, calibration, maintenance, and troubleshooting
  • Assemble and report contract laboratory testing data
  • Assist in the preparation of dossiers and data packages in support of Cellares products for regulatory agencies
  • Other duties as assigned
Requirements
  • BA or B.S. degree in a science discipline required, or comparable experience; M.S. in a scientific discipline is preferred
  • Minimum of 7 years experience in a cGMP or cGxP at an operational level supporting manufacturing in a pharmaceutical or biotech environment
  • At least 2 years in a managerial role
  • Prior experience related to method development/validation preferred
  • Strong background in cell biology, immunology, and molecular biology and associated analytical assays
  • Strong working knowledge of quality systems and regulatory requirements including 21 CFR Part 11/210/211
  • Must have working knowledge of controlled documentation, data systems, cGMPs, SOPs, analytical testing, and auditing
  • Identifying, authoring, and supporting OOS, DRs, and CAPAs
  • Equipment IQ/OQ/PQ experience
  • Proficient in MS Office products including, Word, Excel, Outlook, and Power Point
  • Excellent interpersonal, verbal, written communication and organization skills
  • Self-awareness, integrity, authenticity, and a growth/entrepreneurial mindset
Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.
This is Cellares

Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company’s Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares’ Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.
The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.

Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.


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About Cellares

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

11 - 50 Employees

Headquarters location

South San Francisco, CA, US

Year founded

2019