At a Glance
- Tasks: Lead global regulatory submissions and coordinate cross-functional teams for timely approvals.
- Company: Freyr Life Sciences, a leader in life sciences with a focus on innovation.
- Benefits: Competitive salary, flexible work options, and opportunities for professional growth.
- Other info: Join a dynamic team dedicated to compliance and innovation in healthcare.
- Why this job: Make a significant impact in the life sciences industry while managing exciting global projects.
- Qualifications: 8-15 years in regulatory affairs with strong project management skills.
The predicted salary is between 135900 - 166100 $ per year.
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.
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US Regulatory Submissions Program Manager in Winnipeg 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.
