Associate Regulatory Affairs Jobs in USA

Job Title: Regulatory Affairs Specialist (RA Specialist) Location: Orange County CA (Hybrid) Pay Rate: $38.46/hr $45.67/hr Contract: 6-month contract assignment with potential to be longer A recognized global leader in Assisted Reproductive Technology (ART) is seeking an experien More...

Responsibilities: The Regulatory Affairs Manager is responsible and accountable for Company Core Data Sheets (CCDS) Company Core Safety Information (CCSI) and Reference Safety Information (RSI for assigned products including regulatory responsibilities in associated change control an More...

Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe support of international product registrations and related regulatory affairs activities including execution of procedures and s More...

Eurofins Medical Device Consulting is seeking an experienced and influential Regulatory Affairs Thought Leader to serve as a strategic partner to our marketing and sales teams and a visible representative of our brand in the marketplace. This individual will elevate our presence at tr More...

Transforming what patients can expect from cancer therapy takes passion and a strong dedicated team. When you join ADC Therapeutics you will join a group of talented people who share this missionWhy ADC TherapeuticsADC Therapeutics (NYSE): is a commercial global leader and pioneer in More...

Job Details Norwalk - Norwalk CT $24.00 - $29.00 HourlyDescription Why Join UsAt LBB Specialties we are dedicated to empowering innovation building meaningful relationships and fostering an environment where every team member can thrive. As part of our team youll work alongside indust More...

We anticipate the application window for this opening will close on - 7 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 More...

Job Description SummaryThe Regulatory Affairs / Accreditation Manager (Charleston-Orangeburg/Nexton campus) reports to the Charleston Director for Regulatory Affairs/Accreditation. This position ensures the daily operations of MUSC Health Charleston are conducted in accordance with ho More...

Responsibilities: Prepare and submit new global market device applications and amendments. Prepare and oversee the review of Traditional 510(k) Premarket Notifications. Develop and implement regulatory filing timelines for new and existing products in key markets such as US EU and As More...

Responsibilities: Manage assigned projects to ensure thoroughness accuracy and timeliness of CMC dossiers and responses. Partner with RA CMC Project Leads and develop module 3 content and project timelines. Collaborate with diverse functional groups to ensure file-ability and accepta More...

The Senior Manager Regulatory Affairs Chemistry Manufacturing and Controls (CMC) works with internal and external partners to deliver products to patients. Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submiss More...

Career CategoryRegulatoryJob DescriptionHOW MIGHT YOU DEFY IMAGINATIONYouve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills experience and passion to work toward your goals At Amgen our shared mi More...

Principal Associate Regulatory Risk and GovernanceCapital One is one of the fastest growing organizations in the world today. As a Principal Associate you will apply your risk management and project management skills in our Regulatory Risk and Governance team to support the implementa More...

OverviewSupport the Regulatory Affairs (Executive Director) in developing and executing regulatory strategies for antiviral programs globally or within specific regionsResponsibilitiesAssisting in preparing presentations reports and strategic documents for leadership discussions.Maint More...

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 More...

ABOUT HOUSING CALIFORNIASince 1988 Housing California (Housing CA) has worked to create a California with homes health and prosperity for all in thriving sustainable communities. We bring together a diverse cross-sector network to prevent and end homelessness increase the supply of sa More...

See Yourself at TelixTo support the Groups strategic objectives the Regulatory Affairs Manager Japan will oversee Regulatory Affairs for clinical and commercial registration activities of Telix portfolio in Japan. This role involves conducting regulatory tasks related to new product d More...

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 More...

The Senior 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 analytical skill More...

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). More...