GMP Quality Assurance Analyst
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Quality Assurance - QA/QC
Job Description & How to Apply Below
Pharmavite in Ohio is seeking a Manufacturing Documentation Specialist to ensure quality across GMP manufacturing and packaging operations. You will issue, track, and review documents and records, and collaborate with cross-functional teams to uphold quality standards.
The role emphasizes accurate data handling, attention to detail, and adherence to retention policies while supporting continuous improvement in manufacturing processes.
This posting is for the GMP Quality Assurance Analyst role at Otsuka Pharmaceutical Co., Ltd, based in New Albany, OH, United States.
The position is based in New Albany, OH, United States.
This opportunity is part of our work in Management & Operations, Engineering.
The advertised compensation is 46.000 - 76.000.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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