Job Description: Regulatory and Quality Manager Location: Istanbul, Turkey Department: Regulatory Affairs & Quality Assurance About the Role We are looking for a Regulatory and Quality Manager to ensure end-to-end regulatory compliance across the product lifecycle, while acting as a key interface between regulatory requirements and business operations. This role requires a licensed pharmacist with strong knowledge of Regulatory and Quality frameworks and the ability to work across multiple functional areas including quality, supply chain, and commercial operations. Key Responsibilities Regulatory Affairs & Product Lifecycle Lead regulatory planning in alignment with departmental priorities Manage new product registrations, variations, renewals, and lifecycle maintenance of all marketed products Ensure full compliance of product licenses, certifications, and regulatory filings in accordance with local regulations Maintain accurate and timely regulatory data within global systems Health Authority & External Relations Manage regulatory inspections and ensure continuous inspection readiness Maintain strong professional relationships with relevant authorities and external stakeholders Compliance & Cross-Functional Operations Monitor regulatory changes and assess business impact across functions Ensure compliance with local requirements in areas including product quality, distribution, and pricing governance Support GDP-compliant processes related to product handling and supply chain interfaces Provide regulatory input for pricing, reimbursement submissions, tenders, and market access documentation Quality & Business Support Collaborate with Quality and Supply Chain teams to ensure compliance across product flow and documentation processes Support warehouse and distribution compliance requirements in alignment with regulatory standards Review promotional and non-promotional materials in accordance with local and global regulations Qualifications · University degree in Pharmacy (mandatory) · Licensed Responsible Pharmacist eligibility in accordance with local regulations · Minimum 10 years of experience in Regulatory Affairs and Quality within the pharmaceutical industry · Strong understanding of product lifecycle management and regulatory compliance · Exposure to quality systems, supply chain, or pricing frameworks is a strong advantage · Ability to work cross-functionally and manage multiple priorities · Strong communication skills in English Location: Ferring Turkey Ferring Pharmaceuticals a privately owned, research-driven, specialty biopharmaceutical group committed to building families and helping people live better lives. We are leaders in reproductive medicine with a strong heritage in gastroenterology and urology, and are at the forefront of innovation in uro-oncology gene therapy. Ferring was founded in 1950 and employs more than 7,000 people worldwide. The company is headquartered in Saint-Prex, Switzerland, and has operating subsidiaries in more than 50 countries which market its medicines in over 100 countries. Learn more at www.ferring.com, or connect with us on LinkedIn, Instagram, YouTube, Facebook and X. At Ferring, we'll give you the tools to shape a career build on purpose. Join us and help People around the world to build families and live better lives. Click HERE to enlarge the picture. At Ferring, our focus on Patient Advocacy drives our commitment to create more equitable health outcomes for all, at every stage of their healthcare journey. We believe in everyone’s right to access the best treatment, pioneering into new therapeutic areas, and developing innovative ways to diagnose, treat and prevent diseases. Don't see the dream job you are looking for? Drop off your contact information and resume and we will reach out to you if we find the perfect fit!