Regulatory Affairs Specialist KSA

Regulatory Affairs Specialist KSA page is loaded## Regulatory Affairs Specialist KSAlocations:
Riyadh time type:
Full time posted on:
Posted 2 Days Agojob requisition :
JR014323

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals.

Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story. We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day.

We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee. At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world.

With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.
** Job Title :
Regulatory Affairs Specialist KSA
**** Location : KSA, Riyadh
**** Job Description
** The Regulatory Affairs (RA) Specialist will fulfill the local regulatory activities to maintain & keep the RA portfolio compliant for KSA (70 %) and UAE (30%) .You will support RA Manager on operational RA submissions and assist in ensuring continuous compliance with all RA and Safety Officer responsibilities, maintaining readiness for audits and inspections by Healthcare Authorities at all times

You will ensure business continuity by serving as a backup for the RA Manager, as well as for Quality Assurance (QA) and Pharmacovigilance (PV) functions. As Regulatory Affairs, Quality Assurance, and Pharmacovigilance are mandatory functions that must be continuously available on site—including during vacation periods—you will help ensure that at least one qualified RA/QA/PV representative is present on site at all times.

You will provide strategic and operational Regulatory Affairs support for Saudi Arabia to ensure the timely renewal, maintenance, and variation of existing and new products, including prescription products, injectable aesthetics/medical devices, and cosmetics.

It is critical to maintain momentum to ensure ongoing compliance with the constantly evolving SFDA guidelines.
** Responsibilities
* ** Manage the entire registration process in ensuring approvals of new products and amendments to products
* Develop and execute registration strategy in close partnership with Global RA & local RA Manager
* Stay abreast of, and ensure compliance with, the continuously evolving, complex, and country-specific regulatory frameworks in KSA and the UAE
* Ensure compliance with, and maintenance of, existing product licenses.
* Ensure high-quality, timely regulatory submissions; enhance regulatory intelligence; and develop and maintain databases to simplify local Regulatory Affairs processes, including record retention and submission tracking.
* Ensure that progress of applications and changes to registered details are communicated to local and global stakeholders, as appropriate
* Manage in-house regulatory files, documentation, and corporate electronic databases. Support projects aimed at process improvement and the development of simplification tools across all Middle East markets, including tracking systems and data management. Assist in internalizing certain Regulatory Affairs activities currently outsourced, such as eCTD preparation, in a phased manner.
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