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 samplesWork 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/reportsPrepare COA/COT for testing performedIdentify discrepancies, initiate and investigate OOS/OOT results for phase 1 and phase 2Initiate and investigate deviations related to quality controlCompile and review data to ensure accuracy and regulatory complianceSupport development for specifications and justification of specificationsParticipate in validation and technical transfer of analytical methods commensurate with experienceWrite and revise test methodsMaintain required training and training records and provide training to qualify other associatesParticipate in internal assessments and audits as requiredSupport equipment validation, calibration, maintenance, and troubleshootingWrite method validation protocol/reports and other documentation such as test reportsWrite stability protocol and stability reportsWrite and revise Quality Control Standard Operating ProceduresSupply Quality Control data necessary for regulatory submissionsSupport Quality Systems such as; change control, deviation, CAPA, audits, quality metrics, etc.Assist in general upkeep of the laboratory and maintain a clean work environmentPerform other duties as assigned
Requirements
Bachelor's degree in a science discipline required, or comparable experience2+ years of experience in cGMP or cGxP at an operational level supporting manufacturing in a pharmaceutical or biotech environment, is preferredPrior experience related to method development/validationPrior experience with immune cell phenotyping by multicolor flow cytometry, dPCR, qPCR, cell-based potency and other cell therapy related assays is preferredKnowledge of pharmaceutical cGMP (US and EU) is preferredMust have excellent verbal, written, interpersonal, and organizational and communication skillsMust be able to commute to Bridgewater, New JerseyExcellent verbal, written, organizational, presentation and interpersonal skillsSelf-awareness, integrity, authenticity, and a growth mindset
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.
