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Quality Control In Jobs in New York (NOW HIRING)

Cellares

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 ... All activities are all performed in accordance with cGMP guidelines and are supported by ...

New Cibo Vita LLC

Quality Control Supervisor

Totowa, NJ · On-site

$80K - $90K/yr

Based in Totowa, NJ, we craft premium healthy snacks under the Nature's Garden brand, combining ... The Quality Control Lead will be responsible for supporting the QC Manager in maintaining a high ...

Signetjewelers

QC Associate

New York, NY

$17 - $24/hr

In this role, they will be responsible for ensuring that all jewelry products meet our quality standards and specifications. The ideal candidate has mid-process jewelry manufacturing quality control ...

Union Beverage

Quality Control Batcher

Hillside, NJ

$17.25 - $21/hr

In the event of vacation or extended absence the Quality Control Batcher duties will be covered using overtime(other Quality Control Batcher). * Contributes to team effort by accomplishing related ...

ProCon Homes Inc

Quality Control Inspector

New York, NY

$55 - $67/hr

Join Our Team as a Quality Control Inspector at Procon Homes Inc! Are you passionate about ensuring ... As a trusted name in residential building, remodeling, and project management, we pride ourselves ...

Blue Nile

QC Associate

New York, NY · On-site

$17 - $24/hr

In this role, they will be responsible for ensuring that all jewelry products meet our quality standards and specifications. The ideal candidate has mid-process jewelry manufacturing quality control ...

VSP Vision

Supervisor, Quality Control

Melville, NY · On-site

$58K - $108K/yr

Responsible for the planning, implementation and supervision of procedures and operations of Quality Control and Systems Supervise key functions of quality control operations for all materials in ...

VSP Vision

Supervisor, Quality Control

Melville, NY

$58K - $108K/yr

Responsible for the planning, implementation and supervision of procedures and operations of Quality Control and Systems Supervise key functions of quality control operations for all materials in ...

VSP Vision

Supervisor, Quality Control

Melville, NY

$58K - $108K/yr

Responsible for the planning, implementation and supervision of procedures and operations of Quality Control and Systems Supervise key functions of quality control operations for all materials in ...

RailWorks

Quality Control Manager

Manhattan, NY · On-site

$128K - $155K/yr

Job ID: 19495 Benefits Offering Founded in 1904, L.K. Comstock & Company LLC is one of the largest ... Manages the activities of the quality control team to ensure that the work product meets the ...

Wurth USA

Quality Control Supervisor

Ramsey, NJ · On-site

$55K/yr

This role is responsible for overseeing quality control processes across warehouse operations ... Bilingual in English and Spanish * Proficiency with Microsoft Office * Strong attention to detail ...

CookUnity

Quality Control Supervisor

New York, NY

$22 - $25/hr

So in 2018, CookUnity was founded as the first-of-its-kind platform that connects the world with ... The Role The Quality Control Supervisor is responsible for overseeing the performance of the QC ...

NutraStar Inc

Quality Control Supervisor

Farmingdale, NJ · On-site

$65K - $75K/yr

Our continued investment in people, technology, and infrastructure drives our rapid growth and positions us as a leader in our field. Position Description The Quality Control Supervisor is ...

Wurth USA

Quality Control Supervisor

Ramsey, NJ · On-site

$55K/yr

This role is responsible for overseeing quality control processes across warehouse operations ... Bilingual in English and Spanish * Proficiency with Microsoft Office * Strong attention to detail ...

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Quality Control In information

What is the difference between Quality Control In vs Quality Control Inspector?

AspectQuality Control InQuality Control Inspector
Primary RoleOversees quality assurance processes within production or manufacturing teams, ensuring compliance with standards.Performs inspections and tests on products or materials to identify defects or deviations from specifications.
CredentialsOften requires certifications like ISO or Six Sigma, with experience in quality management systems.Typically requires technical training or certifications such as ASQ Certified Quality Inspector.
Work EnvironmentWorks mainly in manufacturing or production settings, collaborating with quality teams and production staff.Works on the production floor or in labs, inspecting products directly.

While both roles focus on quality, Quality Control In involves managing quality processes and systems, whereas Quality Control Inspectors perform hands-on product inspections. Both roles are essential for maintaining product standards but differ in scope and responsibilities.

What are some common challenges faced by Quality Control Inspectors, and how can they be addressed?

Quality Control Inspectors often encounter challenges such as identifying subtle defects, maintaining consistency across large batches, and managing tight deadlines. Effective communication with production teams and a thorough understanding of product specifications are crucial for addressing these challenges. Leveraging checklists, standardized procedures, and ongoing training can help inspectors stay accurate and efficient. Additionally, embracing new quality management technologies can improve inspection processes and facilitate collaboration with other departments.

What are the key skills and qualifications needed to thrive as a Quality Control Inspector, and why are they important?

To thrive as a Quality Control Inspector, you need a solid understanding of quality assurance principles, attention to detail, and familiarity with industry standards, often supported by a high school diploma or technical certification. Experience with measurement tools (such as calipers and micrometers), inspection software, and knowledge of ISO standards are typically required. Strong analytical thinking, effective communication, and problem-solving skills set top performers apart in this role. These abilities are crucial for ensuring product consistency, meeting regulatory requirements, and maintaining customer satisfaction.

What are Quality Control Inspectors?

Quality Control Inspectors are professionals responsible for examining and testing products or materials to ensure they meet established quality standards and specifications. They work in various industries, including manufacturing, food production, and pharmaceuticals, using specialized tools and techniques to detect defects or deviations. Their role is vital in maintaining product safety, compliance, and customer satisfaction by identifying issues early in the production process. Inspectors document their findings, recommend improvements, and sometimes help implement corrective actions. Their work helps organizations maintain high-quality standards and avoid costly recalls or customer complaints.
What are popular job titles related to Quality Control In jobs in New York? For Quality Control In jobs in New York, the most frequently searched job titles are:
What job categories do people searching Quality Control In jobs in New York look for? The top searched job categories for Quality Control In jobs in New York are:
What cities in New York are hiring for Quality Control In jobs? Cities in New York with the most Quality Control In job openings:
Quality Control In jobs near you
Infographic showing various Quality Control In job openings in New York as of June 2026, with employment types broken down into 75% Full Time, 21% Part Time, 3% Temporary, and 1% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.
Quality Control Analyst

Quality Control Analyst

Cellares

Bridgewater, NJ • On-site

$90K - $210K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 23 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
$90,000 - $210,000 a year
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. 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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