Drive the Future of Biologics at Global Scale – Join my client as the inaugural SVP, leading the strategic, operational, and commercial direction of a pioneering biologics division. You'll have the autonomy and authority to build a world-class CDMO platform — leveraging innovation, deep regulatory expertise, and client-centric excellence—to fuel major growth across the global healthcare market.
Why You Should Apply
Full executive ownership over strategic planning, operations, BD, and P&L.
Opportunity to shape and scale a Bio CDMO backed by a global pharmaceutical leader.
Competitive salary plus full suite of benefits and international career growth.
Influence industry innovation and regulatory excellence (FDA, EMA, ICH).
Be part of a company with 60+ years of trusted pharmaceutical history.
What You’ll Be Doing
Build and lead the full lifecycle of Bio CDMO services from development to GMP manufacturing.
Oversee client onboarding, strategic partnerships, and commercial growth initiatives.
Ensure operational excellence and compliance across all global regulatory frameworks.
Lead financial planning, reporting, and resource optimization initiatives.
Inspire a high-performing cross-functional team across the Americas and beyond.
About You
10+ years of leadership experience in biologics manufacturing or CDMO services.
Master’s degree in a related field (Ph.D. preferred).
Proven success in client acquisition, regulatory compliance, and strategic growth.
Ability to travel domestically and internationally as needed.
How To Apply
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to [email protected] and tell us why you’re interested. Or, feel free to email your resume. Please include Job #19329.
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