At a Glance
- Tasks: Create and coordinate regulatory documents for key market submissions.
- Company: Join Bristol Myers Squibb, a leader in the pharmaceutical industry.
- Benefits: Flexible work options, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on innovation and compliance.
- Why this job: Make a difference in patient safety while developing your writing skills.
- Qualifications: BS/BA in science and 1-2 years of regulatory writing experience required.
The predicted salary is between 35000 - 42000 £ per year.
Bristol Myers Squibb in the UK seeks a regulatory documents writer responsible for coordinating and authoring regulatory documents to support submissions and approvals in key markets.
You will coordinate input from science, medical, and regulatory teams to produce clear, compliant documents.
The role requires a BS/BA in science with 1–2 years of regulatory writing experience, strong writing skills, data interpretation, and MS Office proficiency.
Site-essential or hybrid work options may apply.
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Regulatory Writing Lead, Patient Safety in Uxbridge employer: Meeveem Limited
Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.
