Full-time jobs in Bend, OR

About the role

As a Quality Assurance Associate, you will be responsible for performing the day-to-day tasks of the QA Department supporting a GMP facility manufacturing and testing pharmaceutical products.

What you'll bring

• Knowledge of GMP and FDA regulations for drug manufacturing (21CFR 210-211)
• Excellent verbal and written communication skills
• Excellent time management skills with a proven ability to meet deadlines
• Excellent organizational skills and attention to detail
• Demonstrated ability to collaborate and work in cross-functional teams
• Scientific curiosity and willingness to learn
• Strong analytical and problem-solving skills
• Ability to prioritize tasks and to delegate them when appropriate
• Minimum of a Bachelor's Degree
• 3+ years previous manufacturing, quality control, or quality assurance experience
• Working knowledge of Veeva preferred
• preferably in a scientific discipline

Benefits