Manager, Quality Control

We are seeking an innovative and highly motivated individual to join our team as the Manager of Quality Control at our GMP manufacturing facility located in Bridgewater, NJ. This position will work with the Quality Control team in supporting our efforts in the GMP manufacturing of cellular therapy products. This individual will lead a group of QC analysts performing analytical testing of in-process and final product from cell therapy products. They will interface across different parts of the company to support novel products used in cell and gene therapy. This role will report to the Senior Director of Quality Control. 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 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. Responsibilities Schedule/Manage routine and non-routine analysis of in-process, finished goods, or stability samples Ensure the quality control lab is held to GxP standards and safety standards Create/Review and approve Certificate of Analysis Conduct investigation regarding out of specifications (OOS) results and address and manage deviations related to analytical procedures Review and approve data to ensure accuracy and regulatory compliance Create/Review and approve new and revision of analytical test methods Create/Review and approve method validation protocols/reports and other documentation such as analytical reports Create/Review and approve stability protocols and reports Create/Review and approve quality control operation procedures Manage the validation of analytical methods used in QC as well as the transfer and validation of methods to contract testing laboratories Manage training of other analysts to perform laboratory procedures and assays Participate in internal assessments and audits as required Manage stability program Serve as Quality Control representative during cross-functional/project meetings Serve as subject matter expert between Quality Control and other departments, vendors, or contractors Support Quality Systems such as Change Control, Deviation, CAPA, Audits, Quality Metrics Manage and grow a phase appropriate team of Quality Control personnel Establish user requirements for purchase of new Cellares GMP lab equipment Manage equipment validation, calibration, maintenance, and troubleshooting Assemble and report contract laboratory testing data Assist in the preparation of dossiers and data packages in support of Cellares products for regulatory agencies Other duties as assigned Requirements BA or B.S. degree in a science discipline required, or comparable experience; M.S. in a scientific discipline is preferred Minimum of 7 years experience in a cGMP or cGxP at an operational level supporting manufacturing in a pharmaceutical or biotech environment At least 2 years in a managerial role Prior experience related to method development/validation preferred Strong background in cell biology, immunology, and molecular biology and associated analytical assays Strong working knowledge of quality systems and regulatory requirements including 21 CFR Part 11/210/211 Must have working knowledge of controlled documentation, data systems, cGMPs, SOPs, analytical testing, and auditing Identifying, authoring, and supporting OOS, DRs, and CAPAs Equipment IQ/OQ/PQ experience Proficient in MS Office products including, Word, Excel, Outlook, and Power Point Excellent interpersonal, verbal, written communication and organization skills Self-awareness, integrity, authenticity, and a growth/entrepreneurial mindset

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      "text": "Responsibilities",
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