Senior Quality Assurance Specialist

We are seeking a talented and passionate Senior Quality Assurance Specialist to play a vital role in ensuring the quality and compliance of our product. This individual is detail-oriented and proactive. In this position, this hire will collaborate with various departments, including manufacturing, R&D, and engineering to review documentation, conduct/host audits, investigate deviations and lead projects.

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

• Provides dedicated QA support to client projects and client interactions & meetings; involved from inception of a client’s project until project closure
• Supports Clinical QA activities, including initial process development and non-clinical batch production
• Monitor day-to-day Quality Assurance activities in accordance with approved SOPs/Policies for cGxP integrated contract manufacturing facility
• Ability to troubleshoot, identify process pathways, and develop improvement strategies for site teams on projects/issues
• Understand advanced topics pertaining to cGMP
• Participate in regulatory inspections or customer audits as required
• Understand and articulate company business strategy, maintaining a broad view of the business and recognizing changes and trends
• Review executed batch records and logbooks efficiently to ensure compliance with cGMP per written procedures
• Compile lot genealogy and lot disposition packages, driving lot disposition activities to ensure timely product release
• Provide oversight to product status, including preparation of documents for shipping activities
• Oversee the quality tag-out system
• Actively participate in and approve deviation investigations, utilizing Root Cause Analysis tools for effective and timely closure
• Ensure correct implementation of CAPA based on deviations raised and ensure timely closure of CAPA
• Timely escalation of quality events on the floor based on knowledge of defined SOPs and policies
• Support changeover activities and QA on call
• Provide training to new members and manufacturing teams
• Provide quality oversight for operations document changes (e.g., MBRs, SOPs, forms, logbooks, etc.)
• Provide quality change request oversight for process and operation changes
• Detect non-compliance with cGMP and GDP requirements and provide guidance on GDP corrections
• Revise, review, and approve SOPs, protocols, reports, and records
• Perform any other tasks as assigned
  
  

Requirements

• Bachelor’s degree in a related field (e.g., Life Sciences, Engineering, Quality Assurance, etc.)
• 5-7 years of experience in quality management or quality assurance, preferably in a regulated industry (e.g., medical devices, pharmaceuticals, cell & gene therapy, etc.)
• Strong knowledge with Regulatory requirements and local Codes & Standards (e.g., FDA, EMEA, and ICHQ7)
• Knowledge and experience of the practical and theoretical requirement of quality management system in GMP facility
• Team player who can operate independently, with strong focus on safety, quality and timelines
• Excellent communication, organizational, and analytical skills in a fast-paced, dynamic environment
• Strong attention to detail and commitment to ensuring high standards of quality and compliance
• 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, Free EV Charging, 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.