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A global healthcare company is seeking a Specialist in Regulatory Affairs in Riyadh. The role involves managing compliance with market regulations, compiling regulatory dossiers, and communicating with regulatory authorities. Candidates should have experience in regulatory affairs and excellent communication skills.
Specialist, Regulatory Affairs page is loaded
Responsible for dossier compilation and submission • Responsible for ensuring compliant life cycle management in compliance with market regulations • Manage local Labeling and AWs creation and submission • Maintain the regulatory processes within the department, including assist with the development and implementation of regulatory procedures and SOP, • Manage Communication with regulatory agencies or related interface
Additional Job Description:
Primary Location:
SA RiyadhJob Posting Date:
2025-07-16Job Type:
PermanentMundipharma is a global healthcare company with a presence across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East.
Mundipharma is dedicated to bringing innovative treatments to patients in the areas of Pain Management, Infectious Disease and Consumer Healthcare as well as other severe and debilitating disease areas. Our guiding principles, centered around Integrity and Patient-Centricity, are at the heart of everything we do.
For more information about Mundipharma's guiding principles and commitment to diversity and inclusion visit: www.mundipharma.com/people