Explore 4 Remote Cgmp Regulations Jobs
The R&D Technical Writer will create and review essential documentation for pharmaceutical R&D projects.
The Vice President of Global Manufacturing Operations will lead biologics manufacturing processes while ensuring quality and regulatory compliance.
The Manufacturing Supervisor will lead operations in a newly acquired site, ensuring compliance with cGMP regulations and optimizing production efficiency.
The Manufacturing Supervisor will lead operations in a newly acquired site, ensuring compliance with cGMP regulations and optimizing production efficiency.
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