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MedTech QMS Complaints Lead for Global Implementations

Veeva Systems, Minneapolis, MN, United States


A leading cloud technology company is seeking an experienced consultant to lead MedTech Complaints implementations. The role requires 8+ years of experience in GMP systems, with a strong understanding of FDA and EU regulations. Responsibilities include leading QMS implementations and customer liaison management, all while providing an opportunity to work flexibly either from home or in the office. This position offers a competitive salary range of $80,000 to $200,000, along with additional benefits. #J-18808-Ljbffr