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Manager Qc Jobs (NOW HIRING)

Cellares

Manager, Quality Control

Bridgewater, NJ

$90K - $210K/yr

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 ...

Cellares

Manager, Quality Control

Bridgewater, NJ · On-site

$90K - $210K/yr

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 ...

Newrez LLC

Manager - Quality Control

Bethel Park, PA · On-site

The QC Manager plays a key leadership role in developing quality strategies, managing staff, and continuously improving appraisal review processes to maintain integrity and customer confidence.

Newrez

Manager - Quality Control

Bethel Park, PA

The QC Manager plays a key leadership role in developing quality strategies, managing staff, and continuously improving appraisal review processes to maintain integrity and customer confidence.

TransMedics

Manager Quality Control

Andover, MA · On-site

Overall management of quality control activities; oversee the development and implementation of robust systems and procedures to ensure evaluation, measurement and improvement of processes. * Manage ...

TransMedics

Manager Quality Control

Andover, MA · On-site

Overall management of quality control activities; oversee the development and implementation of robust systems and procedures to ensure evaluation, measurement and improvement of processes. * Manage ...

Dycom Industries, Inc.

Manager Quality Control

Upland, CA · On-site

$90K - $115K/yr

We are looking for a Manager of Quality Control Field who is passionate about building "boots on the ground" excellence and mentoring the next generation of industry experts. Join a team that ...

Cellares

Manager, Quality Control

Bridgewater, NJ · On-site

$90K - $210K/yr

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 ...

Centex Materials

Manager -Quality Control

Austin, TX · On-site

Manage Command QC software working with Concrete Production Manager optimizing materials and training personnel. Manage existing and future Quality Control and Process Control Programs. Communicate ...

StandardAero

Manager, Quality Control

San Antonio, TX · On-site

Quality Control Manager Location: San Antonio, Texas Build an Aviation Career You're Proud Of At StandardAero, we use our ingenuity and know-how to find solutions for the simple to the most complex ...

AAR Corporation

Manager, Quality Control

Miami, FL

... Dale Quality Control Manager.- 30%-50% Travel Required.- All other duties as assigned.SUPERVISORY RESPONSIBILITIES Carries out supervisory responsibilities in accordance with the organizations ...

Quality

Manager, Quality Control (TAS)

Sunrise, FL

Management of QA/QC staff, GMP and ISO compliance. Job Details/Responsibilities * Manages Production Quality staff overseeing Receiving Inspection, Cleanroom, and Final Release areas, including all ...

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Manager Qc information

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$24K

$86.2K

$158K

How much do manager qc jobs pay per year?

As of Aug 19, 2026, the average yearly pay for manager qc in the United States is $86,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $136,000.00 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 cities are hiring for Manager Qc jobs?

Cities with the most Manager Qc job openings:

What are the most commonly searched types of Qc jobs?

The most popular types of Qc jobs are:

What states have the most Manager Qc jobs?

States with the most job openings for Manager Qc jobs include:

Manager Qc jobs near you
Infographic showing various Manager Qc job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $86,159 per year, or $41.4 per hour.

Manager, Quality Control

Cellares

Bridgewater, NJ

$90K - $210K/yr

Full-time

Re-posted yesterday

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

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