We are a public, clinical-stage biotechnology company focused on innovating cell therapies to treat cancer and other incurable diseases. We believe that cell therapies are a cornerstone of future medicine, and our mission is to eradicate cancer and improve human health by developing therapies that are safer, more effective, and accessible.
Our team consists of passionate and talented individuals working from offices in Rockville, Maryland, and Redwood City, California. We pride ourselves on hiring exceptional people and fostering a fun, diverse, supportive, and informal work environment that empowers everyone to do their best work.
Core Values
Character: Always committed to doing what's right.
Audacity: Willing to challenge the status quo and provide candid feedback.
Determination: Curious and self-motivated, constantly striving to improve and learn.
Collaboration: A "no job is too small" mentality; humble and ready to help others.
Originality: Brings a unique perspective while respecting diverse viewpoints.
How You'll Make a Difference
As a Specialist II, MSAT and Manufacturing, your role will be crucial in ensuring the timely delivery of life-saving treatments. You'll contribute to the successful operation of our cell therapy manufacturing facility, and your work will play a key role in advancing transformative therapies for those in need.
Key Responsibilities
Manufacturing Activities
Execute cell therapy manufacturing tasks such as batch production, aseptic processing, and technology transfer.
Follow manufacturing batch records (MBRs) and standard operating procedures (SOPs) in compliance with current Good Manufacturing Practices (cGMPs).
Lead continuous improvement initiatives to optimize operations, reduce deviations, and enhance product quality.
Maintain a clean and organized manufacturing environment to boost productivity and safety.
Documentation and Review
Document all activities in line with Good Documentation Practices (GDPs).
Author and review documents, including MBRs, protocols, deviation reports, and SOPs.
Technical Support and Collaboration
Provide technical support for process changes and validation in T-cell manufacturing.
Participate in risk assessments, gap/facility fit analysis, deviation investigations, change controls, CAPAs, and root-cause analysis.
Collaborate with cross-functional teams (Process Development, Quality Control, Quality Assurance, Facilities, and Supply Chain) to ensure timely product delivery.
Quality & Compliance
Complete all necessary training to maintain quality compliance.
Skills and Experience We Look For
Bachelor's degree in a relevant scientific field and at least 5 years of experience in cell therapy manufacturing.
Strong aseptic techniques and experience with cell processing equipment are preferred.
Ability to work within a clean room environment.
Adherence to cGMP standards.
Strong organizational and prioritization skills.
Excellent collaboration, communication, and interpersonal skills.
Rewards and Benefits
We believe our people are our greatest asset, and we are committed to supporting their well-being. We offer competitive compensation and a comprehensive benefits package:
Base Salary: $110,000 - $120,000 per year (based on experience).
Bonus: Annual bonus based on company goals.
Equity: RSU grant.
Relocation: Assistance available if required.
Benefits Package includes:
100% coverage for medical, dental, and vision for employees and their dependents.
Unlimited vacation and a 3-day weekend every month.