Xcyte Therapies, Inc.

Regulatory Affairs Assistant

Xcyte Therapies, Inc., a Seattle-based biotechnology company, is developing and commercializing novel cell-based or cellular therapeutic products that harness the power of the immune system to treat cancer and many infectious diseases.

This individual will provide a full range of complex regulatory and administrative duties for the Regulatory Affairs Department. Regulatory responsibilities will include, but not be limited to, having sufficient understanding of the CFR to initiate as well as word process routine FDA submissions.

Administrative duties include: proof reading documents, document tracking, database support, managing files and file systems. This position requires working with highly restricted information, so applicants must adhere to policies of strict confidentiality. Exceptional Microsoft Word Processing skills are a must. Proficiency with other computer applications such as Microsoft Office as well as a working knowledge of FDA regulations is needed.

Qualified candidates will have a BA/BS, with at least 2 years work experience in a regulated industry. Previous FDA Regulatory Affairs experience is preferred. Demonstrated ability to multitask and work in a fast paced environment a must. Need accuracy and attention to detail. Familiarity with medical and scientific terminology desired.

Please send resumes to:

Xcyte Therapies, Inc.
Attn: Human Resources
1124 Columbia Street, Suite 130
Seattle, WA 98104
Fax: 206-262-0900
Email: hr@xcytetherapies.com

Xcyte Therapies, Inc. is an Equal Opportunity Employer

Submitted: 04/21/2004