Alnylam Pharmaceuticals is seeking a Senior Manager, Regulatory Affairs to drive planning and delivery of regulatory submissions across EU and international health authorities. The role works with global leads and cross-functional teams to support product development and registrations, including preparation of key regulatory documents and lifecycle submissions.
You will contribute to regulatory strategy, coordinate interactions with regulatory authorities, and mentor teams on submission
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Regulatory Affairs Senior Manager - EU & Global Submissions in Maidenhead employer: Alnylampharmaceuticals
Alnylam Pharmaceuticals is an exceptional employer, offering a dynamic work environment in the heart of the biotech industry. With a strong commitment to employee growth and a culture that values innovation and collaboration, team members are empowered to make meaningful contributions to cutting-edge CNS programs. The company's focus on regulatory excellence and adherence to core values ensures that employees are not only supported in their professional development but also engaged in impactful work that drives advancements in healthcare.
