Quality Assurance Associate II/III

Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products.

Requirements

• 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

Benefits

• Paid Time Off
• Retirement Account
• Health Plans
• Life Insurance
• Long-term Disability
• Employee Assistance Program
• Pet Insurance