Top 6 Quality control raw material analyst Jobs in Rockaway, 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 Lab Technician - Sample Preparation
Vitaquest —West Caldwell, NJ
- From $55,000 a year
- Full-time
- Background check
- Microsoft Excel
- Basic math
- Health savings account
- Health insurance
Quick Apply
2d
Quality Control Analyst
Cellares —Bridgewater, NJ
- $90,000 - $210,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- In-person
- Health insurance
- Dental insurance
QC Analytical Analyst, Raw Materials Testing
Lantheus Medical Imaging Inc —Springfield, NJ
- $72,000 - $107,000 a year
- Microsoft Word
- Mid-level
- Bachelor's degree
- Paid parental leave
- Paid holidays
Quick Apply
QA Auditor II
Intertek —Whitehouse, NJ
- $70,000 - $95,000 a year
- Full-time
- Bachelor of Science
- Basic math
- Pass drug screening
- Health insurance
- Dental insurance
Quick Apply
8d
Senior Scientist, Analytical Chemistry
Amneal Pharmaceuticals —Branchburg Township, NJ
- $90,000 - $123,000 a year
- Full-time
- Bachelor of Science
- Data analysis skills
- Bachelor's degree
- Health insurance
- 401(k) matching

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

Finance Analyst
Branch Insurance —Columbus, OH
Assist in developing financial models and tools that improve claims analysis and forecasting. Present complex information clearly to both technical and non-…
$63,000 - $90,000 a year
Finance Analyst
Branch Financial, LLC —Columbus, OH
Assist in developing financial models and tools that improve claims analysis and forecasting. Present complex information clearly to both technical and non-…
$63,000 - $90,000 a year
Quick Apply

I want to receive the latest job alert for quality control raw material analyst in rockaway, nj

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

quality control raw material analyst jobs near rockaway, nj

Mental Health Technician jobs in Little Rock, AR

Aviation Maintenance Technician jobs in Detroit, MI

Quality Control Lab Technician jobs in Crystal River, FL

Quality Control Lab Technician jobs in Alameda, CA

Data Center Technician jobs in Abilene, TX

Apartment Maintenance Technician jobs in Orlando, FL

Quality Control Lab Technician jobs in Mcminnville, OR

Quality Control Lab Technician jobs in Birdsboro, PA

Quality Analyst jobs in Pearl River, NY

Quality Analyst jobs in Frisco, TX

Food Quality Assurance jobs in Atlanta, GA

Quality Analyst jobs in Tempe, AZ

Quality Analyst jobs in St. Louis, MO

Systems Analyst jobs in Minneapolis, MN

Veterinary Technician jobs in Charleston, SC

Qc Technician jobs in Ohio

Sleep Technician jobs in Wilmington, DE

Qc Technician jobs in Indianapolis, IN

Hvac Technician jobs in Greer, SC

Qc Technician jobs in North Carolina

Quality Control Raw Material Analyst

Cellares
Bridgewater, NJ

Apply Now

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.

Apply Now

Refine Your Search

quality control raw material analyst jobs in rockaway, nj

Quality Control Raw Material Analyst

Quality Control Lab Technician - Sample Preparation

Quality Control Analyst

QC Analytical Analyst, Raw Materials Testing

QA Auditor II

Senior Scientist, Analytical Chemistry

Explore jobs in cities nearby

I want to receive the latest job alert for quality control raw material analyst in rockaway, nj

Explore jobs in more locations

Responsibilities

Requirements

Job Seeker Tools

Employer Tools

Browse

Stay Connected