Freyr Life Sciences in Canada is seeking an experienced Regulatory Project Manager with US submissions experience to lead global filings from planning through approval. You will coordinate cross-functional teams, manage timelines, and communicate with stakeholders to ensure timely submissions.
The role requires 8–15 years in regulatory affairs, independent submission management, and the ability to create study plans, dashboards, and risk logs while maintaining compliance across markets.
US Regulatory Submissions Program Manager in Ottawa employer: Freyr Solutions
Freyr Inc. is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals passionate about regulatory affairs in the biopharmaceutical sector. With a strong emphasis on employee growth, Freyr offers comprehensive training programs and opportunities to lead impactful global initiatives, particularly in the dynamic field of Plasma-Derived Therapies. Located in a vibrant area, employees benefit from a supportive environment that values diversity and encourages meaningful contributions to health authority compliance.
