Responsible for reviewing documentation for batches\rthat are manufactured and packaged. \rAssure compliance with cGMP before being released for\rfurther processing, packaging or commercial market. \r \rEssential Duties & Responsibilities \r1. Review completed\rmanufacturing and packaging documents, as well as laboratory test specification\rsheets. \r2. Ensure all\rpertinent information is compiled, reviewed and approved prior to any product\rdisposition \r3. Identifies\rimprovements/new procedures/ compliance gaps based on applicable regulations. \r4. Assign QA\rstatus (Release/Reject/Quarantine/Impound) to work-in-process and finished\rproduct. \r5. Investigates\rand troubleshoots all routine problems which occur during work assignments. \r6. Coordinate all\rnecessary paperwork for batch release.
\r \r 1 to 3 years experience within a pharmaceutical or\r related manufacturing facility \r \r\r \rEducation Required: \r\r \r 4-year Bachelor’s Degree required\r \r\r\r\r\r\r\r\r\r\r\rKey words:\r\rcGMP, Pharma jobs in Cincinnati, Pharma jobs in Ohio, Quality\rAssurance jobs, Quality Auditor jobs, Pharma Investigation jobs, Pharma QA\rjobs, QA jobs\r\r\r
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Collabera has over 18 years of experience in providing contingent workforce management services and exceeding client expectations through highly effective processes for recruiting, screening, testing, and consultant management. Many of our clients regularly seek our advice when making changes to their internal IT staffing and vendor management programs. Over the years, we have formulated strategies, processes and in-house IT systems - enabling our sourcing engine to mature into one of the strongest in the nation.