Our client focuses on therapies for widespread, chronic diseases, such as central nervous system disorders, addiction, diabetes, and autoimmune disorders. You will have the opportunity to grow your career and make a true difference and the greatest impact!
Located in Wilmington, OH
Pay Rate: $25-30/hr
Shift: Full-time
M-F (8a-5p)
Essential Duties:
- Scanning finished product controlled documents
- Evaluation of raw material records requiring certificate check and verification
- Disposition of raw materials and bulk batches per associated specifications.
- Interact with plant personnel to insure CGMP compliance.
- Provides back up for other QA and plant site personnel as appropriate.
- The monitoring of compliance with the requirement of GMP
- Ability to excel in a team environment
Education& Experience Requirements:Bachelor’s degree in a scientific discipline or equivalent
- 2+ years relevant experience in a Quality Assurance role in the pharmaceutical industry, or equivalent
- Working knowledge of US Drug Product GMP requirements and associated guidelines
