Johnson & Johnson is seeking a Medical Writer II, Regulatory Medical Writing, across multiple countries with a Hybrid work model (3 days onsite weekly). You will author diverse regulatory documents across Oncology, Immunology, Neuroscience, and more, supporting the IDAR team in global regulatory submissions.
The role is located in or near High Wycombe, UK, with potential postings in Beerse, NL, Leiden, and Neuss.
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Regulatory Medical Writer II — Lead Clinical Documents (Hybrid) in High Wycombe employer: Johnson & Johnson
At Johnson & Johnson, we pride ourselves on being an exceptional employer, fostering a culture of inclusivity and respect for diversity. Our Leeds location offers employees the opportunity to work at the forefront of healthcare innovation, with access to comprehensive training and development programmes that support personal and professional growth. Join us to be part of a team that is dedicated to making a profound impact on health for humanity while enjoying a collaborative and supportive work environment.
