Associate Regulatory Affairs Jobs in USA

DescriptionThe Prudential Regulatory Affairs team is tasked with leading strategy on all proposed prudential regulatory policy initiatives affecting relevant JPMC lines of business. The global public policy environment is evolving rapidly driven by technological change evolving and emerging risks an...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The companys R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins and RAS Compa...

Job Summary:The Director of Regulatory Affairs is responsible for executing the companys regulatory strategy across the development and commercial product portfolio. This role reports to the Senior Vice President Regulatory Affairs. This individual serves as the regulatory affairs main contact to pr...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

What Were Looking ForThe Senior Regulatory Affairs Specialist will perform daily tasks under supervision and be responsible for coordinating and managing international shipments to ensure timely compliant and cost-effective importation and exportation of addition this role will adhere to procedures...

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

Application close date:Applications will be accepted on an ongoing basis until the requisition is closed.At Blue Origin we envision millions of people living and working in space for the benefit of Earth. Were working to develop reusable safe and low-cost space vehicles and systems within a culture...

OverviewSr. Regulatory Affairs Operation Specialist (Data Integrity)ResponsibilitiesSupport the governance and review of Regulatory Affairs data integrity while supporting digital transformation projects including standardization of all regulatory affairs data processes and procedures globally. Assi...

Certification Airworthiness Engineering Specialist I (Certification Safety & Regulatory Affairs)in GAC SavannahUnique Skills:This position reports to the Certification Safety & Regulatory Affairs Organization in the Innovation Engineering & Flight OrganizationUnderstanding of regulatory compliance u...

About the job Experience/Knowledge/Technical Skills Required: 1. Around 2 to 5 years of experience in implementation in the QA domain preferably with some experience in working in the Medical Devices industry2. Internal/Lead Auditor of Quality Management Systems3. Knowledge and application skills of...

Roles & Responsibilities1. Implementation and continuous improvement of the Medical Device Quality2. Management Systems and associated CE requirements in order to meet customer3. and regulatory requirements 4. Preparation implementation and Maintenance of Manual policies work instructions as per ISO...

Primary Function of PositionThe Senior Regulatory Affairs Specialist serves as the primary point of contact for regulatory strategy and execution of projects involving complex electromechanical software controlled robotic systems instruments and accessories SaMD and advanced imaging systems. The Sen...

Job SummaryThe Quality & Regulatory Affairs Analyst (Research Engineering Scientist Assoc V) will deliver hands-on quality management and regulatory affairs solutions to a wide range of businesses including manufacturing distribution logistics construction health care and government. Contribute to T...

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesnt just wait for change but actively creates itwhere your skills and valu...

We are seeking an Associate Regulatory Affairs for our North America business. The incumbent will be responsible for maintenance and tracking of regulatory documentation and information pertaining to life cycle management activities; assisting in review of CMC documents for supplements ANDAs NDAs DM...

The Manager Labeling Regulatory Affairs Strategic Labeling develops and maintains US/EU package inserts and Company Core Data Sheets and coordinates review and approval of these documents with changing regulatory environments. The Manager leads discussions to ensure global consistency of labeling an...

The R&D Regulatory Affairs Finance team supports the leadership in strategic planning and execution of both current and long-term goals around resource and budget management. This position is responsible for financial planning and analysis related to Plan Update LRP (Long Range Plan) and Latest Best...

Are you ready to steer US promotional regulatory strategy in a way that accelerates responsible growth and earns patient and prescriber trust This role translates science into clear compliant communication across healthcare professionals consumers and payersso that what we say is as strong as the me...

Are you ready to steer US promotional regulatory strategy in a way that accelerates responsible growth and earns patient and prescriber trust This role translates science into clear compliant communication across healthcare professionals consumers and payersso that what we say is as strong as the me...

Please note that this position can be based in San Diego CA or Princeton NJ. Acadias hybrid model requires this role to work in our office three days per week on average.Position SummaryThe Associate Director Regulatory CMC is responsible for contributing to/assisting with the development and implem...