Lavori di Medicina in Poznan, Polonia
“Regulatory Project Manager role in CMC Excellence team. Lead CMC submission deliverables, author complex regulatory documents, and provide regulatory support for pharmaceutical, biopharm, and vaccine products. Opportunity to work in a hybrid model with flexible hours at (COMPANY NAME), a global biopharma company. Competitive salary and benefits package.”
“* Participate and collaborate in CSV QA initiatives, programs, or team activities, as required.
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