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🚨 HIRING ALERT | GLOBAL REGULATORY LEAD PARTNER 🚨Are you ready to lead global regulatory strategies and drive product registrations across major international markets?Syner-G is looking for a Global Regulatory Lead Partner to support global regulatory operations and lifecycle management activities.Key Responsibilities:Maintain global product registrations across US, EU, and international marketsLead regulatory lifecycle management activitiesDevelop submission strategies and execution plansAssess regulatory risks, challenges, and mitigation strategiesManage regulatory submissions and agency communicationsCoordinate responses to regulatory authority questionsSupport labeling negotiations, updates, and periodic reportingDrive cross-functional collaboration to ensure regulatory compliance and market continuityIdeal Skills & Experience:FDA Regulatory SubmissionsEU MDR & Global RegistrationsRegulatory Strategy DevelopmentProduct Lifecycle ManagementRegulatory Risk AssessmentLabeling ComplianceRegulatory Agency InteractionsGlobal Market AccessTechnical DocumentationMedical Device Regulatory AffairsThis is an excellent opportunity for Regulatory Affairs professionals seeking global exposure, strategic leadership responsibilities, and the flexibility of a remote work environment.
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