Ethypharm is seeking a Senior Regulatory Affairs Officer to lead UK regulatory and CMC lifecycle activities, ensuring compliance with MHRA and EU/international requirements. The role provides strategic regulatory guidance, manages complex post-approval submissions, and mentors junior team members.
You will prepare CTD submissions (Modules 1–5), coordinate with authorities, and liaise with manufacturing, medical affairs, and development teams to align regulatory strategies with business goals.
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Senior Regulatory Affairs Officer – Hybrid, UK employer: Ethypharm
Ethypharm is an exceptional employer located in Romford, offering a hybrid work environment that promotes a healthy work-life balance. With a strong focus on employee growth, we provide comprehensive benefits including generous holiday allowances, a discretionary bonus scheme, and private healthcare options, all within a collaborative culture that values strategic input and mentorship. Join us to be part of a dynamic team where your expertise in regulatory affairs will be recognised and rewarded.
