Merck & Co. is seeking a Quality Design Lead, Drug Product Manufacturing (Associate Director) for the Elkton, VA site. You will shape quality requirements from design through startup, ensuring GMP compliance, contamination control, and high-potent handling across the facility.
The role requires 5–10 years in pharmaceutical quality or related operations, with expertise in cGMP and regulatory expectations. Up to 30% travel in the first two years, then ~10% on-site travel, with a competitive bonus
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