Step into a pivotal role at AbbVie as the Senior Manager of Regulatory Affairs. Oversee submission strategies and ensure compliance for innovative 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 deliverables
- Conduct performance reviews and feedback sessions
- Coordinate pre-submission meetings with Health Canada
- Develop Canadian labeling and submission strategies
- Manage documentation within regulatory systems
Requirements:
- Degree in Pharmacy or a related Life Sciences field
- Minimum of 10 years in the pharmaceutical sector
- Experience leading teams for 4+ years
- Established success with regulatory submissions
- Solid organizational and interpersonal skills
Harness your expertise in regulatory affairs to influence AbbVie’s impactful product development.
📌 Lead Regulatory Affairs Manager Role (Montreal)
🏢 AbbVie
📍 Montreal
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.