Clinical Quality Assurance Intern

Who We Are 

Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible.  

Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work.  

What Matters to Us 

Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. 

Arcellx Core Values 

• Character: Committed to always doing what’s right.  

• Audacity: Willing to challenge convention and share candid feedback with others.  

• Determination: Curious and self-motivated. Always looking to improve and learn.    

• Collaboration: "No job is too small" mentality. Humble and willing to help others.  

• Originality: Will bring your unique perspective to the table and respect a diverse set of views and backgrounds.  

The “Fine Print” – What You’ll Do  

• Assist in the development of clinical quality documents, including standard operating procedures (SOPs) and audit reports. 

• Support the preparation and execution of internal and external clinical audits. 

• Help develop, track and analyze Key Quality Indicators and metrics to identify areas of process improvement. 

• Collaborate with cross-functional teams to support quality planning and training initiatives. 

Skills and Experience We Look For  

Our ideal candidate is/has: 

• Pursuing or recently completed a degree in Life Sciences, Pharmacy, Public Health, Regulatory Affairs, or a related field. 

• Strong analytical skills with attention to detail. 

• Excellent verbal and written communication skills. 

• Ability to work independently and collaboratively in a fast-paced environment. 

• Proficiency in Microsoft Office (Word, Excel, PowerPoint). 

• Prior knowledge of GCP regulations is a plus but not required.  

Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to www.arcellx.com.  

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