Akorn Pharmaceuticals
Categories
Manufacturing, Production & Wholesale
About Us
A niche generic pharmaceutical company engaged in the development, manufacture & marketing of multi-source and branded pharmaceutical products in the areas of ophthalmology.
Jobs
QA Technician I, Documentation Systems
Category: Administrative & Office Work
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This position is responsible for revising and maintaining controlled documents including, but not limited to: Master Batch Records, Standard Operating Procedures, Active Pharmaceutical Ingredient Specifications, Finished Drug Product Specifications, Forms, and Protocols. Maintain and distribute Document Change Requests.
Additional duties include:
Develop, generate, track and issue
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Quality Manufacturing Associate
Category: Manufacturing
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This position can be on either 2nd or 3rd shift. The Quality Manufacturing Associate (QMA) performs quality assurance checks of documentation in the assigned areas to prevent potential failures in compliance and product sterility during in process operations.
Review in-process and completed batch records and documentation for completeness, accuracy and integrity.Follow up with
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