This position will provide support for and be directly responsible for a range of Quality Assurance/Qualified Person functions. This position will contribute to ensure that performance of manufacturing, packaging operations and drug product contract manufacturing organizations (CMOs) and product quality conforms to established cGMPs to ensure lasting customer satisfaction. This individual will demonstrate a high level of involvement in continuous improvement of the quality assurance philosophy and practice to ensure the right standards are implemented.

MAIN DUTIES

• Review of batch records for accuracy and completeness
• Review and approve all Master Batch Records used in manufacturing and packaging operations
• Disposition and release of product manufactured and/or packaged on site or by 3rd Party Manufacturers & New Product Introduction Products
• Collaborate in the execution of cGMP-training program.
• Prepare and Participa...