Precigen is a dedicated discovery and clinical stage biopharmaceutical company advancing the next generation of gene and cell therapies using precision technology to target the most urgent and intractable diseases in our core therapeutic areas of immuno-oncology, autoimmune disorders, and infectious diseases. . Precigen has developed novel manufacturing processes to deliver UltraCAR-T® and AdenoVerse™ immunotherapies to patients. We have multiple...
Precigen is a dedicated discovery and clinical stage biopharmaceutical company advancing the next generation of gene and cell therapies using precision technology to target the most urgent and intractable diseases in our core therapeutic areas of immuno-oncology, autoimmune disorders, and infectious diseases. . Precigen has developed novel manufacturing processes to deliver UltraCAR-T® and AdenoVerse™ immunotherapies to patients. We have multiple...
Precigen is a dedicated discovery and clinical stage biopharmaceutical company advancing the next generation of gene and cell therapies using precision technology to target the most urgent and intractable diseases in our core therapeutic areas of immuno-oncology, autoimmune disorders, and infectious diseases. Precigen has developed novel manufacturing processes to deliver UltraCAR-T® and AdenoVerse™ immunotherapies to patients. We have multiple p...
Precigen is seeking a highly motivated and skilled. Project. Management Associate. to work with our Regulatory Affairs team in Germantown, Maryland. The Regulatory Project Management Associate will be responsible for supporting complex filing activities, ensuring compliance with technical and regulatory standards. This role involves strategic thinking, efficient resource management, and clear communication with stakeholders and the project team. ...
Responsibilities. Primary Focus: Review QC Analytical Data Packs and QC Micro Data Packs. Secondary Focus: Review Stability timepoint Reports. Tertiary Focus: Review EM data packs. Other: Logbook Review to reduce backlog. . Desired Background. 5 years in QA (pharmaceutical industry). Experience in QC Analytical (review or lab work) is highly preferred. Excellent communication skills and ability to work with different departments to make correctio...
