QIAGEN in Manchester is seeking a Senior Clinical Submission Specialist to join Clinical Affairs. You will support preparation of high‑quality submission documentation for IVDR products, ensuring compliance with global regulatory requirements and cross‑functional collaboration.
The role requires strong attention to detail, scientific writing skills, and experience in regulatory submissions within the IVD/medical device space. Hybrid work is available with competitive benefits.
#J-18808-LjbffrEU IVDR Submissions Lead – Clinical Affairs (Hybrid) in Manchester employer: QIAGEN
QIAGEN is an exceptional employer that fosters a collaborative and innovative work culture, perfect for those passionate about advancing Life Science research. With a strong focus on employee growth, you will have access to ongoing training and development opportunities, alongside a competitive benefits package that includes private healthcare and flexible working options, making it an ideal place to thrive in the Midlands & South Wales region.
