Ipsen Biopharm Ltd. is seeking a Regulatory Submission Project Manager to coordinate global regulatory submissions, ensure timeliness and compliance, and work with Regulatory Affairs, Clinical, Quality and Manufacturing teams across regions.
The role requires managing submission plans for new marketing authorisations and indications, applying project management principles, and driving continuous improvement in submission quality and efficiency.
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Global Regulatory Submissions Lead employer: Ipsen Biopharm Ltd
Ipsen Biopharm Ltd is an excellent employer, offering a dynamic work environment in Wrexham where innovation and compliance are at the forefront of pharmaceutical manufacturing. Employees benefit from a strong commitment to health and safety, opportunities for professional growth, and a culture that values continuous improvement and teamwork. Joining Ipsen means being part of a dedicated team that plays a crucial role in delivering high-quality drug substances while enjoying the support and resources needed to thrive in your career.
