A career at Merck is an ongoing journey of discovery: our 50,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. For 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.
Your role: Lead the CMC development program team in order to drive and set the CMC strategy and activities of the relevant molecule(s), delivering quality products and processes with appropriate validation and regulatory documentation for a “Right First Time” submission, and within agreed timelines and budget. Represent the Global Biotech Development function within the R&D global team of the assigned molecule(s), providing options and innovative solutions to drive the project forward, with full transparency of timelines and costs. Set the strategy, drive, facilitate and manage all process and product development activities within Global Manufacturing & Supply in order to provide the agreed deliverables. Serve as the interface between the R&D Global Team and the Global Manufacturing & Supply Functions. Build, manage and control the programme related cost. Monitor the preparation and review the CMC section of regulatory dossiers and lead CMC interaction with regulatory agencies . Serve as interface with the Global Regulatory Affairs group. Be the interface with CMOs/CROs for the development activities. Drive risk management through risk assessment and the development of mitigation plan(s).
Who you are:
What we offer: At Merck, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!
Curious? Apply and find more information at come2merck.com