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Quality Control Stability Manager Jobs in Springfield, NJ

Cellares

Quality Control Analyst

Bridgewater, NJ

$90K - $210K/yr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... Operating Procedures * Supply Quality Control data necessary for regulatory submissions * Support ...

Tutorperini

QA/QC Manager

New York, NY

$185K - $200K/yr

The salary range for this position is between $185,000 - $200,000 depending on experience Tutor Perini is seeking a QA/QC Manager to join the project in Manhattan, NY. About Manhattan Jail Project ...

Cellares

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... Operating Procedures * Supply Quality Control data necessary for regulatory submissions * Support ...

WSP

Quality Control Fuels Manager

Manhattan, NY · On-site

This Opportunity WSP is hiring for a Quality Control Fuels Manager to support work at DoD sites ... stability throughout the employee's career. At WSP, we want to give our employees the challenges ...

WSP

Quality Control Fuels Manager

Manhattan, NY · On-site

This Opportunity WSP is hiring for a Quality Control Fuels Manager to support work at DoD sites ... stability throughout the employee's career. At WSP, we want to give our employees the challenges ...

CookUnity

Quality Control Supervisor

New York, NY · On-site

This role involves managing the QC team, planning audits, coordinating with cross-functional departments, and maintaining documentation that supports food safety, labeling accuracy, and efficient ...

Zion Contracting

Be Seen First

Construction Quality Control Manager

Brooklyn, NY · On-site

$70K - $110K/yr

We are searching for a Construction Quality Control Manager for a project located in Brooklyn, NY. The candidate is responsible for managing and performing the daily QC responsibilities of specific ...

Group PMX

QA/QC Field Manager

New York, NY · On-site

$145K - $170K/yr

Job Title: QA/QC Field Manager Location: Brooklyn, NY (On-site, 5 days per week) Salary Range: $145,000- $170,000 annually Position Overview The BOD QA/QC Field Manager serves as the Owner ...

New Cibo Vita LLC

Quality Control Supervisor

Totowa, NJ · On-site

$80K - $90K/yr

The Quality Control Lead will be responsible for supporting the QC Manager in maintaining a high level of customer and consumer satisfaction by assuring consistent quality. The ideal candidate will ...

Aerotek

Quality Control Technician

East Brunswick, NJ · On-site

$18.75 - $24/hr

Quality Control Technician The Quality Control Technician supports a food manufacturing production ... stability and opportunities to grow with the business. The work environment is structured and ...

Wurth USA

Quality Control Supervisor

Ramsey, NJ

$55K/yr

Support the Distribution Center Manager and provide leadership coverage as needed * Help foster a ... Monitor and enforce quality control standards across all warehouse functions * Oversee process ...

Wurth USA

Quality Control Supervisor

Ramsey, NJ · On-site

$55K/yr

Support the Distribution Center Manager and provide leadership coverage as needed * Help foster a ... Monitor and enforce quality control standards across all warehouse functions * Oversee process ...

Suffolk Construction

QA/QC Manager

Manhattan, NY · On-site

$127K - $178K/yr

The Construction QA/QC Manager position is a primary role where an individual is directly responsible for the implementation and management of applicable quality control plan(s) as directed by the ...

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Showing results 21-40

All JobsQuality Control Stability JobsQuality Control Stability Manager JobsQuality Control Stability Manager Jobs in Springfield, NJ

Quality Control Stability Manager information

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$31.8K

$84.7K

$134.9K

How much do quality control stability manager jobs pay per year?

As of Aug 18, 2026, the average yearly pay for quality control stability manager in Springfield, NJ is $84,685.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,000.00 and $104,100.00 per year, depending on experience, location, and employer.

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Quality Control Stability Manager jobs near you
Infographic showing various Quality Control Stability Manager job openings in Springfield, NJ as of August 2026, with employment types broken down into 67% Full Time, 22% Contract, and 11% Nights. Highlights an 100% In-person job distribution, with an average salary of $84,685 per year, or $40.7 per hour.

Quality Control Analyst

Cellares

Bridgewater, NJ

$90K - $210K/yr

Full-time

Re-posted 8 days ago

Job description

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 testing according to Standard Operating Procedures (SOPs).  This role supports the day-to-day operations within the Quality Control group via execution of analytical testing. This includes but is not limited to in-process testing, lot release testing, stability testing, and raw material testing. All activities are all performed in accordance with cGMP guidelines and are supported by departmental and inter-departmental policies and standard operating procedures.
 
This role will be a hands-on resource reporting to the Senior Director, Quality Control Bioanalytics.  
 
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
  • Conduct routine and non-routine analytical, biochemical, and/or biological analysis such as, in-process materials, raw materials, finished goods, or stability samples
  • Work with cell therapy products and associated assays (dPCR, qPCR, cell-based potency assays, proliferation assays, ELISA, flow cytometry assays, etc.)
  • Perform timely and accurate peer review of analytical test results/reports
  • Prepare COA/COT for testing performed
  • Identify discrepancies, initiate and investigate OOS/OOT results for phase 1 and phase 2
  • Initiate and investigate deviations related to quality control
  • Compile and review data to ensure accuracy and regulatory compliance
  • Support development for specifications and justification of specifications
  • Participate in validation and technical transfer of analytical methods commensurate with experience
  • Write and revise test methods
  • Maintain required training and training records and provide training to qualify other associates
  • Participate in internal assessments and audits as required
  • Support equipment validation, calibration, maintenance, and troubleshooting
  • Write method validation protocol/reports and other documentation such as test reports
  • Write stability protocol and stability reports
  • Write and revise Quality Control Standard Operating Procedures
  • Supply Quality Control data necessary for regulatory submissions
  • Support Quality Systems such as; change control, deviation, CAPA, audits, quality metrics, etc.
  • Assist in general upkeep of the laboratory and maintain a clean work environment
  • Perform other duties as assigned
Requirements
  • Bachelor's degree in a science discipline required, or comparable experience
  • 2+ years of experience in cGMP or cGxP at an operational level supporting manufacturing in a pharmaceutical or biotech environment, is preferred
  • Prior experience related to method development/validation
  • Prior experience with immune cell phenotyping by multicolor flow cytometry, dPCR, qPCR, cell-based potency and other cell therapy related assays is preferred
  • Knowledge of pharmaceutical cGMP (US and EU) is preferred
  • Must have excellent verbal, written, interpersonal, and organizational and communication skills
  • Must be able to commute to Bridgewater, New Jersey
  • Self-awareness, integrity, authenticity, and a growth 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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