Top 110 Quality control inspectors Jobs in Somerset, Nj

Quality Control Raw Material Analyst
Cellares —Bridgewater, NJ
- $90,000 - $210,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- Cleaning
- Health insurance
- Dental insurance
Quality Control (QC) Analyst I, II, & III
Kashiv BioSciences, LLC —Piscataway, NJ
- $70,000 - $95,000 a year
- Full-time
- English
- Mid-level
- Bachelor's degree
- Travel reimbursement
- Health savings account
Quality Control Technician
LeMaitre —North Brunswick, NJ
- Full-time
- Microsoft Outlook
- Mid-level
- High school diploma or GED
- Opportunities for advancement
Data Reviewer I
Ohm Laboratories Inc , USA —New Brunswick, NJ
- $65,000 - $77,000 a year
- English
- Analysis skills
- Bachelor's degree
- Disability insurance
- Health insurance
Senior Quality Control Inspector (Incoming Materials) (Spector)
Veeco —Somerset, NJ
- $51,900 - $65,700 a year
- Microsoft Word
- Microsoft Excel
- 6 years
- Commuter assistance
- Employee stock purchase plan
Mechanical Quality Control Inspector
A&A Coatings —South Plainfield, NJ
- $16 - $26 an hour
- Overtime
- Computer literacy
- Pass drug screening
- English
- Profit sharing
- Health insurance
Quick Apply
Auditor I
Formosa Plastics Corporation, USA —Livingston, NJ
- $56,921.00 - $74,149.75 a year
- Full-time
- Microsoft Excel
- English
- Office
- Paid holidays
- Disability insurance
Quality Control Technician
Quadrangle Products Inc. —Englishtown, NJ
- From $19.50 an hour
- Full-time
- US work authorization
- In-person
- Manufacturing
- Health insurance
- Dental insurance
Quick Apply
9d
QC Inspector
RIchards Mfg Co —Irvington, NJ
- $16 an hour
- 8 hour shift
- Microsoft Word
- Spanish
- Microsoft Excel
- Health insurance
- Dental insurance
Quick Apply
Quality Control Technician II
United Premium Foods, LLC —Woodbridge, NJ
- $19 - $21 an hour
- Full-time
- Background check
- Spanish
- Microsoft Excel
- Health savings account
- Health insurance
Quick Apply
Quality Specialist
MRP Solutions —Township of Franklin, NJ
- $24 - $26 an hour
- Full-time
- Mid-level
- Ability to climb stairs
- Analysis skills
Quick Apply
4d
Quality Lab Analyst
Givaudan —East Hanover, NJ
- $24 - $25 an hour
- 12 hour shift
- Computer literacy
- Data analysis skills
- English
- Health insurance
- Dental insurance
Quick Apply
Warehouse Returns Associate
Focus Camera —North Brunswick, NJ
- $16 - $17 an hour
- Full-time
- Computer literacy
- US work authorization
- Data entry
- Health insurance
- Dental insurance
Quick Apply
2d
QA Bulk Inspector
Vitaquest —Parsippany-Troy Hills, NJ
- From $20 an hour
- Full-time
- Background check
- Computer literacy
- Basic math
- Health savings account
- Health insurance
Quick Apply
2d
QC Supervisor
Cosmax USA —Carteret, NJ
- $25 - $27 an hour
- Full-time
- Background check
- 5 years
- High school diploma or GED
- Health insurance
- Dental insurance
Quick Apply
Foodservice Quality Control Associate
Sovereign —Cranford, NJ
- $17.50 an hour
- Full-time
- English
- US work authorization
- In-person
Quick Apply
Scientist I, Quality Control
WuXi Biologics —Cranbury, NJ
- $60,000 - $960,000 a year
- Weekends as needed
- Maintenance
- Mid-level
- Master's degree
Quality Control Technician
Princeton BioMeditech Corporation —Princeton, NJ
- Associate's degree
- Entry level
QA INSPECTOR I
ASPIRE PHARMACEUTICALS INC —Somerset, NJ
- Full-time
- High school diploma or GED
- Continuous improvement
- 1 year
Quick Apply
IPQA Associate I
Ohm Laboratories Inc , USA —New Brunswick, NJ
- $30 - $37 an hour
- Monday to Friday
- Microsoft Excel
- Microsoft Outlook
- English
- Disability insurance
- Health insurance
9d

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Quality Control Raw Material Analyst

Cellares
Bridgewater, NJ

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Job Details

Full-time
$90,000 - $210,000 a year

Benefits

Stock options
Health insurance
Dental insurance
Vision insurance
401(k) matching

Qualifications

USP standards
Pharmaceutical regulatory compliance
ICH guidelines
Bachelor's degree
Cross-functional collaboration
Cross-functional communication

Full Job Description

We are seeking a detail-oriented and operationally rigorous Quality Control Raw Material Analyst to join our Quality Control (QC) team in Bridgewater, New Jersey.

The primary focus of this position is to support raw material incoming inspection, sampling, and compendial testing activities for cGMP manufacturing operations at Cellares' Smart Factory. This spans the end-to-end raw material quality workflow: receiving, inspection and sampling of incoming materials, coordinating sample shipment to internal and external testing laboratories, reviewing test results to support disposition, and performing in-house compendial and physicochemical testing in accordance with USP, EP, and applicable pharmacopeial standards. All activities are performed in compliance with cGMP requirements and guided by departmental SOPs and cross-functional quality systems.

This is a hands-on, laboratory-facing role reporting to the Senior Manager, QC Raw Materials

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

Perform incoming inspection of raw materials, components, and single-use systems in accordance with approved sampling plans and acceptance criteria (e.g., AQL-based plans per ANSI/ASQ Z1.4)
Execute material sampling using aseptic or clean techniques as appropriate; prepare and label samples in compliance with chain-of-custody and traceability requirements
Verify Certificate of Analysis (CoA), Certificate of Conformance (CoC), and other supplier documentation against purchase orders, specifications, and approved supplier qualification records
Place materials on quarantine hold in the QMS and coordinate with warehouse/materials management for physical segregation
Coordinate and track material dispositions (approve, reject, conditional release) in the ERP/QMS system
Prepare sample shipments to external contract testing organizations (CTOs) and internal satellite labs, including proper packaging, temperature monitoring, and regulatory documentation (e.g., IATA compliance for biological or hazardous materials as applicable)
Maintain sample shipping logs and ensure traceability from sample collection through receipt confirmation at the receiving lab
Communicate with external testing labs regarding sample receipt, testing timelines, and result delivery; escalate delays or anomalies to the QC Manager
Perform compendial testing including but not limited to: pH (USP <791>), osmolality, conductivity, appearance/visual inspection (USP <790>), and FTIR (USP <854>)
Operate and maintain QC instruments; perform instrument calibration checks, cleaning, and basic troubleshooting in accordance with maintenance schedules
Prepare test solutions, reagents, and standards; verify reagent identity, expiry, and suitability prior to use
Execute testing per approved test methods and SOPs; record data contemporaneously in batch records, logbooks, or electronic systems
Review and perform peer verification of raw material test results (CoA, external lab reports, in-house data) against approved specifications prior to disposition
Identify Out-of-Specification (OOS) and Out-of-Trend (OOT) results; initiate formal investigations in the QMS and participate in root cause analysis as required
Ensure all raw data, calculations, and documentation meet ALCOA+ data integrity principles
Author, review, and revise SOPs, work instructions, and forms related to raw material sampling, testing, and inspection activities
Initiate and participate in deviation investigations and CAPAs associated with raw material or testing nonconformances
Support change control activities, including assessment of changes to raw material specifications, sampling plans, or testing methods
Maintain training records and complete all required GMP training in a timely manner; provide hands-on training to qualify new associates in sampling and testing procedures
Support internal audits and external regulatory inspections; assist with preparation of audit-ready documentation
Contribute to quality metrics reporting (e.g., raw material rejection rates, testing turnaround times, OOS frequency)

Requirements

Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or a related science discipline required; comparable experience may be considered
2+ years of hands-on experience in a cGMP pharmaceutical, biotech, or CDMO/IDMO environment, with direct experience in raw material or incoming quality control functions preferred
Working knowledge of USP compendial methods relevant to raw material testing (e.g., <645>, <785>, <790>, <791>, <854>)
Familiarity with pharmacopeial standards and raw material qualification frameworks (USP, EP, ICH Q3C, ICH Q3D) is a plus
Experience with AQL-based sampling plans and statistical sampling methodologies preferred
Prior experience coordinating sample shipments to external CTOs, including documentation and cold-chain logistics, preferred
Proficiency in electronic QMS, ERP, and/or LIMS systems (e.g., Trackwise, SAP, LabVantage or equivalent)
Strong attention to detail and commitment to data integrity and contemporaneous documentation
Excellent written and verbal communication skills; ability to communicate effectively with cross-functional teams and external laboratory contacts
Must be able to commute to and work on-site in Bridgewater, New Jersey
Self-awareness, integrity, authenticity, and a growth/entrepreneurial 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 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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Refine Your Search

quality control inspectors jobs in somerset, nj

Quality Control Raw Material Analyst

Quality Control (QC) Analyst I, II, & III

Quality Control Technician

Data Reviewer I

Senior Quality Control Inspector (Incoming Materials) (Spector)

Mechanical Quality Control Inspector

Auditor I

Quality Control Technician

QC Inspector

Quality Control Technician II

Quality Specialist

Quality Lab Analyst

Warehouse Returns Associate

QA Bulk Inspector

QC Supervisor

Foodservice Quality Control Associate

Scientist I, Quality Control

Quality Control Technician

QA INSPECTOR I

IPQA Associate I

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