Looking for someone with big pharma GMP experience

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Does anyone on here have experience managing, working in, or doing QA in a commercial pharmaceutical facility? My partners and I are looking to build out a DEA-licensed manufacturing operation. It is essential to have someone with experience working in an environment that was regulated by all the FDA-relevant rules in the CFR.

I know a lot of cannabis operations are “GMP” but the ideal person would have some non-cannabis experience on their resume, especially with regards to all the very detailed and regulated recording-keeping practices required in the CFR.

If this sounds like you, or someone you know, shoot me a message! Cheers!

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21 CFR 210/211 are the pertinent regs you need for Pharma/API cGMP (as opposed to cosmetics or supplements).

Best of luck.

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Yes, I worked for several years for a global pharmaceutical company. Title 21 CFR part 211. FDA audits. I have also worked several years in regulated cannabis. Currently working in biotech making therapeutic DNA and RNA. The company complies with 211 CFR 21

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