Biopharmaceutical CMC provides independent, objective GMP analytical testing for manufactured medicinal products from late discovery through post-market approval on behalf of global clients. With a strong portfolio of clients and over 25 years of expertise this team provides advanced characterization, method development, stability and routine QC release for biologics, vaccines, ATMP's, and a breadth of other complex biomolecules. The Mechelen site is designed to offer clients enhanced access to CMC state‑of‑the‑art analytical testing. This role is EU‑based and will be closely tied to the launch and commercial success of the new Mechelen facility. * Prospect, develop, and expand relationships with clients evaluating outsourcing of CMC testing. * Lead client meetings, including Bid Defense, capabilities presentations, governance meetings, and relationship reviews.
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