Prepare high-quality scientific and technical documentation, such as reports, risk assessments, and development packages for internal and external (e.g., Quality, Regulatory Affairs, CDMOs) * Represent Drug Product Process Development in internal and external meetings and scientific exchanges * Build and manage strong relationships with internal teams and external , including CDMOs, CROs, and licensing partners * Individual development and career paths, internal trainings and participation in international conferences and scientific events
mehr