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In this role, you will be responsible for pharmaceutical manufacturing process validation. Leading the validation team for the process validation in the chemical plants. Ensuring...
Provide Quality oversight of internal and external GxP operations, e.g. Drive, lead and troubleshoot quality investigations at internal and external partners to ensure that all...
As the Associate Director, Regulatory Affairs CMC you will be responsible and accountable for Regulatory CMC development, registration, and post-approval strategies. You will...