Step into a pivotal role at AbbVie as the Senior Manager of Regulatory Affairs. Oversee submission strategies and ensure compliance for cutting-edge medical solutions in various therapeutic fields.In this leadership position, you will guide a talented team responsible for navigating the complexities of Canadian regulations. Your strategic insights will directly impact the successful launch of AbbVie's products. Collaborate with departments across the organization to streamline processes and enhance regulatory efficiency.Key Responsibilities:Supervise regulatory project timelines and deliverablesConduct performance reviews and feedback sessionsCoordinate pre-submission meetings with Health CanadaDevelop Canadian labeling and submission strategiesManage documentation within regulatory systemsRequirements:Degree in Pharmacy or a related Life Sciences fieldMinimum of 10 years in the pharmaceutical sectorExperience leading teams for 4+ yearsEstablished success with regulatory submissionsStrong organizational and interpersonal skillsHarness your expertise in regulatory affairs to influence AbbVie's impactful product development.#J-18808-Ljbffr

📌 Lead Regulatory Affairs Manager Role (Montreal)
🏢 AbbVie
📍 Montreal