Regulatory Affairs and Quality Assurance Manager – MENA

Regulatory Affairs and Quality Assurance Manager – MENA page is loaded## Regulatory Affairs and Quality Assurance Manager – MENAlocations: Dubai, United Arab Emiratestime type: Full timeposted on: Posted Todayjob requisition id: R562288Work Flexibility: Hybrid**Regulatory Affairs and Quality Assurance Manager – MENA**As a **RAQA Manager** with Stryker, you will play a critical leadership role in driving regulatory and quality excellence across a dynamic and fast-growing region. Based in Dubai, this position offers a unique opportunity to act as a strategic partner to the business while ensuring compliance and operational effectiveness across key markets such as the UAE, Saudi Arabia, Egypt. You will be at the forefront of shaping regulatory strategy, supporting business growth, and leading high-performing teams within a global, matrix organization known for innovation and impact in healthcare.**What You Will Do:*** Collect, organize, and maintain files on local, regional, and global RAQA intelligence* Identify the need for new regulatory procedures and SOPs, and participate in their development, implementation, and continuous improvement across RAQA* Provide support to EMEA/Country RAQA teams, as appropriate, by defining and executing local RAQA strategy in alignment with EEMEA and local sites* Act as RAQA Leader, reporting performance, risks, and issues to local leadership teams and other Stryker leadership teams, where applicable* Define targets, KPIs, and performance objectives for RAQA within the local office* Maintain a high level of team engagement, development, and collaboration across the RAQA team in the local office* Lead the integration of new acquisitions, ensuring RAQA systems integration within the local office and across EMEA, depending on the integration strategy* Represent Stryker in regulatory working groups at local or regional trade associations, identify needs for broader international collaboration, and leads regulatory changes together with key internal and external partners**What You Need:*****Required:**** BSc degree in a relevant field* 8+ years of related experience, including a minimum of 3 years of supervisory experience* Demonstrated knowledge and application of regulatory requirements, including Medical Device Directive, EU Medical Device Regulations, Quality Systems, and Post-Market Surveillance requirements, as well as other international medical device regulations* Proven leadership skills, including experience in managing remote team, developing talent and managing complex, multi-region projects within a matrix environment* Strong project and time management skills, including writing, coordination, and execution of complex RA/QA/PMS activities* Fluency in English* Arabic language proficiency**Preferred:*** Advanced degree or RAC certificationDiversity is important to us. We welcome applications from people regardless of their ethnic, national, or social origin, gender, disability, age, or sexual identity.Please note that the internal job title may differ from the ad title.Travel Percentage: 20%#J-18808-Ljbffr