Cellares

Quality Control Analyst

Bridgewater, NJ · Director

Sponsorship not specified$90k-$210kDetected 424 days ago

Code ReviewComplianceGMPqPCRFlow CytometryProtein Analysis

About the role

This position will be responsible for routine and non-routine QC testing according to Standard Operating Procedures (SOPs).
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.

Perform timely and accurate peer review of analytical test results/reports
Support development for specifications and justification of specifications
Support equipment validation, calibration, maintenance, and troubleshooting
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

Maintain required training and training records and provide training to qualify other associates
Participate in internal assessments and audits as required

We are seeking an innovative, creative, and detail-oriented Quality Control Analyst to join our team in Bridgewater, New Jersey.
This role supports the day-to-day operations within the Quality Control group via execution of analytical testing.
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.

This listing is sourced directly from Cellares's careers page and normalized into a canonical job model.