Shift: 8AM-5PM or 8:30am-5:30pm (Flexible)
Pay: $19.23-$23.08 (Depending on Experience)
Key Responsibilities:
Issuing and reviewing MBRs in support of Production schedule
Issuing/confirming Lot Expiration Dates of Raw Materials, Components and Finished Products
Create, review and apply QA Release Labels
Review QC results detailed per SOPs, RMSs and PRSs
Ensure approved documents (MBRs, SOPs, TLFs) are issued and controlled
Ensure Controlled Records are controlled and easily retrievable
Initiating proposed changes as Document Circulation Requests and Sage Change Requests
Perform Visual Inspection of Raw Materials, Foil/Label Inspection and AQL testing
Ensure Non-Conformities and CAPA are identified, investigated and controlled
Initiate Non-Conformity documentation and determine the Quality Impact. Deliver New Hire Training
Approve Lot Expiration Dates
Disposition Pre-Raw/Raw Materials, Components, and Finished Goods
Approve Manufacturing/Packaging MBRs
Complete projects as assigned by QA Manager or QA Supervisor
Qualifications and Experience:
High School Diploma +2 years of experience in GMP/FDA environment
Associate's degree + 1 year of experience in GMP/FDA environment
B.A. or B.S.
Life Science degree preferred but not required
Must be able to lift upwards of 30lbs