وظائف Associate Regulatory Affairs في الولايات المتحدة
وظائف Associate Regulatory Affairs في الولايات المتحدة

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Global Regulatory Affairs Manager
BandLevel 4Job Description Summary#LI-Hybrid #LI-OnsiteIn this role you will be a part of the Regulatory team within Navigate and will be primarily responsible for providing strategic product direction as well as directing and coordinating the submission of regulatory documents for r المزيد...
Sr. Regulatory Affairs Specialist
Job Summary: The Sr. Regulatory Affairs Specialist plays a critical role in ensuring regulatory compliance and supporting cross-functional teams in the preparation submission and tracking of regulatory documentation. This position requires strong collaboration communication and analyt المزيد...
Global Regulatory Affairs Manager
Job Description Summary#LI-Hybrid #LI-OnsiteIn this role you will be a part of the Regulatory team within Navigate and will be primarily responsible for providing strategic product direction as well as directing and coordinating the submission of regulatory documents for regulated IV المزيد...
Regulatory Affairs Labeling Specialist - Irvine
We anticipate the application window for this opening will close on - 26 Jul 2025At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a m المزيد...
Responsibilities: The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design manufacturing and sales of medical devices (including Class I and II devices software as a medical device). المزيد...
Associate Director, Regulatory Affairs Cmc
Cytokinetics is a late-stage specialty cardiovascular biopharmaceutical company focused on discovering developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performa المزيد...
Associate Principal Scientist (associate Director) Regulatory Affairs
Job DescriptionGRACS CMC Associate Principal Scientist CMC R4 Pharm Pre-approval Reporting to the Sr Director/Director/Principal Scientist/Sr Principal Scientist in Pre-approval Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our compa المزيد...
OverviewThe Director Regulatory Affairs is responsible for leading the day-to-day activities of Regulatory Affairs with specific emphasis on global regulatory submission strategy regulatory submissions adverse event reporting / field actions and interaction with global regulatory auth المزيد...
Specialist, Regulatory Compliance
Bring more to life.Are you ready to accelerate your potential and make a real difference within life sciences diagnostics and biotechnologyAt Leica Biosystems one of Danahers 15 operating companies our work saves livesand were all united by a shared commitment to innovate for tangible المزيد...
Responsibilities: In this critical role you will lead regulatory strategies product submissions and a team of talented regulatory affairs professionals to drive timely product approvals and ensure ongoing regulatory compliance in key markets such as USA (FDA) EU (MDR) China (NMPA) an المزيد...
Responsibilities: Regulatory Labelling Documentation. Support the creation and maintenance of assigned labelling projects to enable worldwide regulatory submissions. Independently prepare and maintain the Tracking Sheets for the global regulatory dossiers related to labelling project المزيد...
We are looking to hire an Associate Veterinarian to join our practice.Requirements Doctor of Veterinary degree or equivalent from an accredited university Active Veterinary State License (preferred) Benefits Innovative associate health and wellbeing department (Headspace app s المزيد...
Senior Administrative Assistant - Regulatory Affairs (office-based)
The Senior Administrative Assistant will support the broader Regulatory Affairs organization including Strategic Medical Writing and Ad Promo. The Senior Administrative Assistant is responsible for all administrative functions of the department: answering phones managing calendars sch المزيد...
Summary:Provides regulatory support to all preapproval and post approval activities for new products and existing products through products lifecycle. Prepares and compiles drug product regulatory documents. Provides regulatory guidance to matters related to product development.Primar المزيد...
Principal Regulatory Affairs Specialist - Crm
We anticipate the application window for this opening will close on - 4 Aug 2025At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a mo المزيد...
Senior Regulatory Relations AssociateCountry: United States of AmericaYour Journey Starts Here:Santander is a global leader and innovator in the financial services industry. We believe that our employees are our greatest asset. Our focus is on fostering an enriching journey that empow المزيد...
Responsibilities: Supports necessary regulatory activities required for product market entry. Preparation of regulatory submissions for Electrophysiology Mapping and Imaging devices to achieve departmental and organizational objectives. Review and approve engineering change orders fo المزيد...
Responsibilities: Maintain full awareness of all regulatory activities on assigned Project(s) and ensure that the project deadlines and performance standards for these projects are established and met. Also work with internal and external stakeholders to manage submission schedules. المزيد...
Responsibilities: Regulatory Labelling Documentation. Support the creation and maintenance of assigned labelling projects to enable worldwide regulatory submissions. Independently prepare and maintain the Tracking Sheets for the global regulatory dossiers related to labelling project المزيد...
Responsibilities: Preparing documentation for international regulatory registrations. Preparing technical documentation to compliant to MDD and EU MDR. Defining worldwide regulatory requirements are necessary for regulatory approval of products. Participating in cross functional team المزيد...
اذا كنت تبحث الان عن وظائف في مجال Associate Regulatory Affairs في الولايات المتحدة - San Diego, Sunnyvale, Chicago - اكتشف 565 فرصة عمل وظائف مختلفة مثل مدير الشؤون التنظيمية, أخصائي الشؤون التنظيمية, موظف شؤون تنظيمية, مدير الشؤون التنظيمية المساعد, مساعد مراقبة الجودة على دكتور جوبس، أفضل بوابة وظائف في الخليج. استكشف فرص وظيفية جديدة في مختلف الصناعات مثل تصنيع المنتجات الصيدلانية, البحوث في التكنولوجيا الحيوية. اختر بحرية نظام عملك المفضل من Full-time, عن بُعد, عقد، قم برفع مستوى تجربتك المهنية مع دكتور جوبس، أكبر موقع وظائف في منطقة الشرق الأوسط وشمال إفريقيا. افتح أمامك فرص جديدة اليوم لتنمية خبراتك ومهاراتك العملية.
جوب هي منصة إلكترونية تربط أصحاب العمل بالباحثين عن عمل من ذوي المهارات، مما يسهل عملية البحث عن فرص العمل وإيجاد أفضل المواهب. أنشئت في عام 2015. و برزت كبوابة الوظائف الرائدة في جميع دول العالم، حيث تجتذب الآلاف من الباحثين عن عمل يوميًا من جميع أنحاء العالم
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