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
