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