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QA Manager
•30 days ago
| Hours | Full-time, Part-time |
|---|---|
| Location | CLINTON, SC CLINTON, South Carolina |
About this job
This role is responsible for the cGMP aspects of the entire manufacturing operation.
Administering the MBR (Master Batch Record) program for all of the technical operations (Extraction/Formulation/Filling) is a primary objective.
They are responsible for the overall testing of the extraction and formulation batches and the assurance of purity and purported potency of the commercial products.
Responsible for the CV (Cleaning Validation program) and handling all aspects of the CAPA (Deviation and corrective action) process.
This role would also be responsible for the tracking/control of any controlled substances and responsible for any such reporting to the proper agency.
B.S. Analytical Chemistry, Organic Chemistry, Chemical Engineering or other science. 7+ years working in a pharmaceutical or other regulated industry doing liquid/capsule filling, QA management is preferred. Experience and understanding of quality systems, cGMP s and the CFR is required. Experience with general equipment validation, cleaning validation and process validation is a plus.
We are a EEOC compliant employer
APSTECHNICALSERVICES
Additional Information
We are an Equal Opportunity Employer and follow all Federal and State employment laws. Engineering and Technical Positions at www.apstechnical.com
Administering the MBR (Master Batch Record) program for all of the technical operations (Extraction/Formulation/Filling) is a primary objective.
They are responsible for the overall testing of the extraction and formulation batches and the assurance of purity and purported potency of the commercial products.
Responsible for the CV (Cleaning Validation program) and handling all aspects of the CAPA (Deviation and corrective action) process.
This role would also be responsible for the tracking/control of any controlled substances and responsible for any such reporting to the proper agency.
B.S. Analytical Chemistry, Organic Chemistry, Chemical Engineering or other science. 7+ years working in a pharmaceutical or other regulated industry doing liquid/capsule filling, QA management is preferred. Experience and understanding of quality systems, cGMP s and the CFR is required. Experience with general equipment validation, cleaning validation and process validation is a plus.
We are a EEOC compliant employer
APSTECHNICALSERVICES
Additional Information
We are an Equal Opportunity Employer and follow all Federal and State employment laws. Engineering and Technical Positions at www.apstechnical.com
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