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

Polysciences, Inc.

Quality Control Analyst I

Warrington, PA · On-site

$23.50 - $31.75/hr

We adhere to ISO13485:2016, FDA cGMP 21 CFR 820 regulations, and SOCMA's ChemStewards ® Management System. We believe the best scientific innovations are built through collaborations. The QC Analyst ...

Ott Scientific

Quality Control Analyst I

Warrington, PA · On-site

$59K - $69K/yr

We adhere to ISO13485:2016, FDA cGMP 21 CFR 820 regulations, and SOCMA's ChemStewards ® Management System. We believe the best scientific innovations are built through collaborations. The QC Analyst ...

AMA-ALU CORP

Quality Control Supervisor

Hatfield, PA · On-site

Lead internal audit program and manage third-party audit readiness, including pre-assessment gap ... Experience with quality systems, statistical process control (SPC), and root cause analysis tools

Penn Color, Inc.

QC Technician

Hatfield, PA · On-site

$19 - $24.25/hr

Penn Color is looking for a QC Technician - Dry to join our Quality Control team in Hatfield, PA. This role supports quality control operations by preparing test samples, operating lab-scale ...

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All JobsQuality Control JobsQuality Control Manager JobsQuality Control Manager Jobs in Riverside, NJ

Quality Control Manager information

See Riverside, NJ salary details

$30.8K

$82.1K

$130.8K

How much do quality control manager jobs pay per year?

As of Aug 13, 2026, the average yearly pay for quality control manager in Riverside, NJ is $82,136.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,100.00 and $101,000.00 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 cities near Riverside, NJ are hiring for Quality Control Manager jobs? Cities near Riverside, NJ with the most Quality Control Manager job openings:
Quality Control Manager jobs near you
Infographic showing various Quality Control Manager job openings in Riverside, NJ as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 19% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $82,136 per year, or $39.5 per hour.

Quality Control Analyst I

Polysciences, Inc.

Warrington, PA • On-site

$23.50 - $31.75/hr

Full-time

Re-posted 26 days ago

Job description

Polysciences technical operations and scientific laboratories offer custom synthesis, contract manufacturing and packaging, and laboratory products. We are proud to offer a broad range of products and tailored solutions for the life sciences, bioprocessing, microparticles, medical device, specialty chemical and eChem industries. We adhere to ISO13485:2016, FDA cGMP 21 CFR 820 regulations, and SOCMA’s ChemStewards® Management System. We believe the best scientific innovations are built through collaborations.

The QC Analyst I is responsible for performing incoming raw materials, in-process samples, intermediate products, and final products analytical analysis per approved internal and customer specifications following associated procedures to support both product manufacturing and commercial product release. Will work under the supervision of more experienced analysts and follow established procedures and protocols.

Essential Functions:

  • Performs routine analytical analysis using the following equipment: volumetric glassware, balances, pH Meter, Conductometer, Karl Fisher (KF), TOC, Turbidimeter, GC (FID/MS), Atomic Absorption (AA), and others as required.
  • Responsible for QC data analysis and data entry, using both electronic systems and hard copy documentation following GDP.
  • Ability to effectively communicate with cross-functional teams, including production, quality assurance, and planning.
  • Reports OOS results to QC Manager or designee and assists with compiling required information to complete the investigation report.
  • Performs daily and monthly analytical equipment verification and maintenance. 
  • Flexibility to handle unexpected situations and make adjustments to ensure compliance with 820 GMP and ISO 13485 standards.
  • Assists on the review and revision of procedures and test methods.
  • Assists on laboratory inventory maintenance.
  • Maintains a safe, clean, and organized environment (5S) for all QC areas.
  • Supports process improvements within the QC laboratory.

Qualifications:

  • Bachelor’s degree in chemistry or related science field required.
  • At least one (1) year of experience working in an ISO 13485 or FDA GMP regulated environment preferred.
  • At least one (1) year of experience working in an ISO 13485 or FDA GMP regulated environment preferred.
  • Experience with quality control GMP documentation of analytical testing results and assurance of laboratory data integrity and compliance preferred.
  • Knowledge of analytical equipment, analytical methods, and data analysis required.
  • Knowledge of compendial methods (ie. USP, EP, ISO, ASTM) preferred.
  • Experience with Open Lab, Chem Station and/or Empower analytical software preferred.
  • Proficiency with Adobe, Microsoft Word and Excel required.

Qualifications

Education Required: Bachelor's Degree Preferred: Bachelor's Degree

Certification(s): Specify preferred or required.

Computer Skills Required: Specify preferred or required.

Experience with Open Lab, Chem Station and/or Empower analytical software preferred.

Proficiency with Adobe, Microsoft Word and Excel required.

Other qualifications:

  • Bachelor's degree in chemistry or related science field required.
  • At least one (1) year of experience working in an ISO 13485 or FDA GMP regulated environment preferred.
  • Bachelor's degree in chemistry or related science field required. At least one (1) year of experience working in an ISO 13485 or FDA GMP regulated environment preferred.
  • Experience with quality control GMP documentation of analytical testing results and assurance of laboratory data integrity and compliance preferred.
  • Knowledge of analytical equipment, analytical methods, and data analysis required.
  • Knowledge of compendial methods (ie. USP, EP, ISO, ASTM) preferred.

Immediate Work Environment:

X-Chemicals Unprotected Height X-Fumes/Gases Persistent Noise

X-PPE used: Lab Coat, Safety Shoes, and Safety Glasses

Work Activity: [must equal number of hours worked per day]

Stand: 4 Frequency: Intermittently Walk: 1 Frequency: Intermittently

Sit: 3 Frequency: Intermittently Drive: 0 Frequency: Choose an item.

Lift/Carry Demands

Frequency: Lift/Carry Equipment Provided:

0-10 lbs. 1-3 hours a day Reagents Bottles Carriers

11-25 lbs. Not Daily Rolling Cart

26-50 lbs. Rarely Gas Tank Hand Cart/Drum Lift Cart

51-75 lbs. Never Click or tap here to enter text.

76-100 lbs. Never Click or tap here to enter text.

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