Description
Under the supervision of the Reagent Manufacturing Document Manager, works with the Reagent Manufacturing team to create and revise manufacturing documents. Documents include work instructions (WIDs), standard operating procedures (SOPs), etc. to ensure they are in harmony with the manufacturing process and comply with regulatory standards. Also creates and updates change control documents for these processes, and coordinates and supports the validation of manufacturing batch records.
Essential Job Duties and Responsibilities:
- Perform all work in compliance with company policy and within the guidelines of Biomerieux SLC’s Quality System.
- Creation and revision of cGMP documentation including Production… Click here to view original post
