Employment Opportunities

QC Associate

Requires:

• Able to perform mostly routine analysis with detailed documentation for both R & D and cGMP Manufacturing samples. Also includes some specific testing and non–routine project analyses.
• Attention to detail, problem solving ability, good time management, reliability, and flexibility.
• cGMP training is highly desirable.
• Good communication skills with legible handwriting a must.
• General knowledge of laboratory safety is required.
• 2–4 years laboratory experience.
• Scientific background with emphasis on chemistry; B.A. or B.S. preferred.

Duties

• Perform routine sample analysis for chemical purity and identification using HPLC, GC, etc.
• Perform detailed, accurate documentation
• Communicate in a friendly and collaborative manner
• Perform other duties as assigned

To apply send a completed application with cover letter to:

Please — no recruiters or phone calls

AVI BioPharma, Inc. is an Equal Opportunity Employer