Associate Director, Global Regulatory Affairs and Clinical Safety, External Operations / Supplier
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
Merck is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases.
This position will be responsible for supporting the development and implementation of multi-year sourcing strategy with external partners across the Global Regulatory Affairs and Clinical Safety organization at Merck. Additionally, this position will be responsible for directing the activities in support of our current (and future) outsourced scope of work.. Responsibilities will include managing processes and connections between the external partner and the various stakeholders within MRL including Global Regulatory Affairs and Clinical Safety (GRACS) Functional Area Managers, GRACS-Leadership and the regulatory and clinical safety teams to ensure that we are efficiently and effectively delivering high quality regulatory and safety submissions on time globally. Additionally, the incumbent will need to have a close working relationship with Procurement as part of effective execution of the sourcing management process.
- Associate's Degree
- Project Management
- Regulatory Affairs, Supplier Management
Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life.
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Job: Regulatory Affairs Generic
Employee Status: Regular
Travel: Yes, 15 % of the Time
Number of Openings:
Shift (if applicable):
Company Trade Name: Merck