Lead regulatory initiatives at Roche as a Regulatory Program Manager, ensuring efficient interactions with Health Authorities to support innovative treatments. This role is hybrid, with a focus on collaboration.As a key member of Roche's regulatory team, you will manage the execution of comprehensive regulatory strategies that bring life-changing therapies to market. Your expertise in biologics and technical regulatory practices will be instrumental in compiling high-quality submissions and engaging effectively with global regulators. This position fosters a strong collaborative environment for professional growth.Key Responsibilities:• Oversee the submission of high-quality regulatory documents• Conduct strategic meetings with health authorities for submissions• Collaborate with internal teams on synthetic and biologic products• Support completion of cross-functional deliverables on time• Enhance regulatory excellence by identifying process improvementsRequirements:• Life sciences Bachelor’s degree; advanced degree preferred• 3+ years in technical regulatory or manufacturing roles• In-depth knowledge of biologics manufacturing and lifecycle• Strong analytical and communication skills• Experience in building trusted cross-functional relationshipsJoin Roche in Mississauga to influence healthcare through impactful regulatory strategies.#J-18808-Ljbffr
Pharma Technical Regulatory Program Manager
F. HOFFMANN-LA ROCHE GRUPPE
mississauga, mississauga
Published 18 days ago
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