MD/IVD Regulatory Consultant — Medical Devices & CDx
A global pharmaceutical reputed company is seeking a consultant specialized in regulatory expertise for Medical Devices and In-Vitro Diagnostics. The role focuses on improving regulatory processes, managing change for reputed company, and implementing global regulatory strategies. Candidates should have extensive knowledge of EU and US medical device regulations, especially in relation to Combination products and Companion Diagnostics. This is a W2 position requiring approximately 30 hours per week, with reputed company and benefits available.
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