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Role Summary
Head of Global Biopharma Technical Development
Responsibilities
Deliver Chemistry, Manufacturing, and Controls (CMC) packages for biopharmaceuticals on time and at the right quality.
Lead and develop a global, multi-disciplinary team of scientists while maintaining strong stakeholder partnerships across Product Development, Regulatory, Manufacturing, and Quality.
Set the vision and strategy for ElancoβΓΓ΄s biotechnology platforms, fostering a culture of high technical rigor and innovation.
Oversee technical transfer of new products and processes into commercial supply sites (internal and external).
Manage resources, budgets, and external networks (CDMOs, consultants) to deliver against portfolio timelines and milestones.
Qualifications
Required: Ph.D. in chemistry, engineering, or a biotechnology-related field.
Required: Minimum of 10 years of relevant experience working with biologics.
Required: Strong technical leadership and collaboration skills, with proven ability to influence cross-functional teams and deliver outcomes in regulated environments.
Preferred: Experience establishing Process and Analytical Control Strategies for biologics.
Preferred: Demonstrated ability to lead and develop diverse scientific teams across geographies.
Preferred: Strong track record in building development timelines for process and analytical method development.
Preferred: Familiarity with regulatory agencies (FDA, USDA, EMA).
Preferred: Proven success in managing major projects and implementing innovative technical strategies.
Skills
Technical leadership
Cross-functional collaboration
Regulated environment experience
Strategic thinking and planning
Education
Ph.D. in chemistry, engineering, or a biotechnology-related field
Additional Requirements
Location: Indianapolis, IN, USA βΓΓ¬ Global Headquarters
Travel: Up to 20% (global site support and external collaborations)