Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence, and love of challenge. With a presence in more than 70 countries - and growing - we look for talented people to grow our business, advance our science, and contribute to our unique culture.

This position is responsible for supporting commercial product definition, leading process development, scale-up, registrational stability batch mfg., technology transfer, supporting validation, and providing in-line technical support.

Responsibilities will include, but are not limited to, the following:

• Key member of a dynamic scientifically driven team, dedicated to the development and optimization of robust manufacturing processes for drug products.
• Serve as Drug Product Development team lead and represent the team on multidisciplinary CMC teams.
• Leverage understanding of formulation design and development to support commercial product definition.
• Develop process development strategies to define manufacturing processes for commercialization.
• Responsible for the design and execution of complex experiments to characterize drug product manufacturing processes utilizing various technologies.
• Ensure fundamental engineering principles are applied to characterize and solve process challenges across multiple unit operations, utilizing both experimental and process simulation/modeling approaches.
• Lead the identification, development, and deployment of new instrumentation, technologies, and methodologies to support efficient and effective drug product process development.
• Manage drug product process development/technology transfer to Contract Research/ Manufacturing Organizations.
• Provide technical support for clinical manufacturing.
• Prepare technical reports, publications and oral presentations and contribute to the preparation of CMC regulatory documents.
• Serve as a resource of scientific and technical expertise.
• Coach and develop scientists/engineers under a project specific matrix team.
• Assume departmental responsibilities for assigned projects and equipment.
• Maintain safety, regulatory, and compliance standards as they relate to the development of pharmaceuticals.