Description
1. Conducts real time batch record reviews in assigned areas.2. Verifies line clearance of product path areas.
3. Pulls samples from the line and performs product inspections. Documents results in the batch record.
4. Pulls required number of file and stability samples based on the QA sampling instructions for the lot.
5. Monitors assigned area for compliance to SOPs and cGMPs - equipment, documentation and personnel.
6. Performs compliance audits of manufacturing and warehouse areas.
REQUIREMENTS:
-High School Diploma or equivalency
-3 years of pharma industry experience
-2 years in Quality role, or Associates's Bachelor's degree with 2 years pharma industry experience
-familiar with GMP's, master formulas, batch records, monographs, etc.
-ability to preform calculations- fractions, decimals, rounding, rations, proportions
-maintain applicable certifications
-utilize good jodgement when preforming compterized system taks
-be able to work independently
-good communication skills
To find out more about Real please visit www.realstaffing.com