Job Description
Quality Assurance Associate
JOB DESCRIPTION:
The ideal candidate will work cohesively and effectively with others to deliver excellence in written/verbal communications, planning, documenting, organizing, and executing multiple tasks simultaneously in a high paced environment. Will conduct other quality tasks as required.
Review and Disposition Duties
Document Control Duties:
Qualifications:
· Bachelor’s Degree or higher in a life science or related disciple or 2 years GMP experience
· 2+ years in a quality role
· Preferred experience of review & disposition or working directly in sterile environment
· Strong attention to detail
· Knowledge of FDA and USP guidelines
· Excellent oral and written communication skills
· Responsiveness, reliability, ability to express assurance/confidence, professionalism.
· Team-oriented and customer service focused.
· PC skills in Windows-based applications, ability to learn new software.
Confidentiality
The employee must maintain the confidentiality of company information and, pursuant to State and Federal Law (including the Health Insurance Portability and Accountability (HIPAA) Act of 1996), protected health information.
EOE/ADA
Carie Boyd Pharmaceuticals is an Equal Opportunity Employer. In compliance with the Americans with Disabilities Act, Carie Boyd Pharmaceuticals will provide reasonable accommodations to qualified individuals with disabilities and encourages both prospective and current employees to discuss potential accommodations with the employer.
Company DescriptionWe specialize in compounding office-use and personalized prescription medications.
We specialize in compounding office-use and personalized prescription medications.
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