Advance your career at Freyr Life Sciences as a Regulatory Project Manager specializing in US submissions. Your project management skills will be crucial in guiding complex regulatory processes for life sciences companies.

At Freyr Life Sciences, we are seeking an experienced Regulatory Project Manager with 8-15 years of background in regulatory submissions. Your responsibilities will involve coordinating cross-functional teams, developing and maintaining project timelines, and managing submissions through their lifecycle. Solid leadership and organizational skills are essential for ensuring successful outcomes.

Key Responsibilities:
• Manage the lifecycle of US regulatory submissions
• Co-lead teams and facilitate kickoff meetings
• Develop and maintain submission timelines collaboratively




• Keep thorough records of decisions and action items
• Conduct lessons learned sessions for continuous improvement

Requirements:
• 8-15 years in regulatory affairs/project management
• Experience with Microsoft Project or Smartsheets is advantageous
• Proficient with Microsoft Office software
• Ability to effectively manage multiple priorities
• Strong understanding of regulatory frameworks in life sciences

Bring your regulatory expertise and project management skills to Freyr Life Sciences, supporting impactful regulatory submissions.
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📌 Regulatory Project Manager in Life Sciences (Manitoba)
🏢 Freyr Solutions
📍 Manitoba