A biopharmaceutical company is seeking a GRA Device Lead for their Global Regulatory Affairs team. The role involves developing regulatory strategies for medical devices and leading submissions throughout the product lifecycle. Ideal candidates should have over 8 years in the pharmaceutical or medical device industry, with strong regulatory experience and familiarity with health authority interactions. The position requires collaboration across R&D, Manufacturing, and Quality teams, and adaptability in a fast-paced, hybrid work environment.
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