Regulatory Document Specialist

Responsibilities;Maintain organized records of financial and customs documents in line with internal and regulatory requirements Support the payment process by collecting, checking, and submitting all required documentation to the bank Reconcile customs declarations and supplier invoices, ensuring data accuracy and timely posting Coordinate with internal...

Regulatory Affairs SpecialistWe are seeking a highly motivatedRegulatory Affairs Specialistto join our Import team on the European side of Istanbul.If you have a strong background in Turkish Food Legislation and managing complex import processes for food products, we invite you to apply. The Role: Key ResponsibilitiesThe Regulatory Affairs Specialist will be...

Operating Company: DEXISLocation: Istanbul,Istanbul,TRDate Posted: November 11, 2025Req Number: R5024578Job Description:Interprets federal/state/international regulations as they apply to our products, processes and/or procedures advises on impact of regulations, devises strategies for compliance, and liaison with regulatory bodies. Investigates and resolves...

Job DescriptionInterprets federal/state/international regulations as they apply to our products, processes and/or procedures advises on impact of regulations, devises strategies for compliance, and liaison with regulatory bodies. Investigates and resolves compliance problems, questions and complaints. Audits and evaluates current policies, procedures, and...

Job DescriptionResponsibilities;Maintain organized records of financial and customs documents in line with internal and regulatory requirementsSupport the payment process by collecting, checking, and submitting all required documentation to the bankReconcile customs declarations and supplier invoices, ensuring data accuracy and timely postingCoordinate with...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure...

A Global Company in Medical Devices SectorGreat Opportunity for Regulatory ProfessionalsClient DetailsOur client is a multinational pharmaceutical company with a strong and specialized product portfolio, recognized for its commitment to scientific excellence and patient-focused innovation.DescriptionManage UTS notifications and SUT registration processes...

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About Us:Proceutica is a pharmaceutical company established in 2008, specializing in rare diseases and orphan drugs. Through strong global partnerships, we provide innovative therapeutic solutions to support patients with unmet medical needs. With a dynamic structure and a commitment to high ethical standards, we continue to expand our presence in the...

What You'll Do:Independently manage essential regulatory documentation (as applicable) for submission to country/regional/site Institutional Review Boards (IRB), Ethics Committees (EC), Competent Authorities (CA) and/or other Regulatory Bodies for all clinical studies performed globally. Interact with, assist and advise study teams, site personnel, sponsors,...