QA Associate
Artech Information System LLC
- Morris Plains, New Jersey, United States
- Morris Plains, New Jersey, United States
About
Ensure that all aspects of the operational business comply with cGMP legal and regulatory requirements, the Client Pharma Corporate Quality Manual and Policies, and site procedures and business requirements. Coordinate and perform batch record issuance for internally manufactured products. Review and approve manufacturing and QC related documents for raw material disposition, manufactured media. Perform administrative functions for filing and maintenance of records between QA operations and Document Control Center; support cGMP and associated OJT training to QA and other departments to improve "Right the First Time" (RTFT) and high quality performance. Control costs within the department to meet budget. Complete job-related training in electronic database system along with GMP, safety, and Ethics & Compliance course requirements. Perform or support any other tasks necessary to maintain the product quality and site cGMP compliance, as needed. Qualifications
0‑3 years GMP manufacturing and/or QA related experience. BS/BA in Biological Sciences or equivalent relevant career experience.
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Languages
- English
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