Manager, Quality Control

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

$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.