Associate Regulatory Affairs Jobs in USA

Your New Company!At Altasciences we all move in unison to assist and work in the discovery development and manufacturing of new drug therapies to get them faster to people who need them. No matter your role we all play an important part and you will have a significant impact on the health and well-b...

DescriptionHoneywell is currently hiring an experienced a Lead Executive Administrator who will provide administrative and organizational support to Honeywell Aerospaces Deputy General Counsel who is responsible for Compliance Litigation Intellectual Property and ESG located in Charlotte North Carol...

Application RequirementsIn order to be considered for this position applicants must successfully submit a completed application prior to the posting deadline. Applications submitted with incomplete or missing education and/or work experience sections will be considered incomplete and will not be rev...

Primary Function of PositionThis position will partner with the in-country RA team as well as the Product Localization Engineering (PLE) and other cross-functional supporting teams make sure the companys regulatory affairs activities are conducted in accordance with company policies and in complianc...

Primary Function of PositionThis position will partner with the in-country RA team as well as the Product Localization Engineering (PLE) and other cross-functional supporting teams make sure the companys regulatory affairs activities are conducted in accordance with company policies and in complianc...

Do you have knowledge in Regulatory Affairs Strategy and Policy underpinned with experience transformingDigitalprocesses with AI and automationIf you want to work on innovative projects of high importance for our Respiratory and Immunology(R&I)portfolio then AstraZeneca is the place for aspiration...

QualificationsRequires an advanced degree of JD (or international equivalent legal degree) and admission to relevant regulatory bar and/or active practicing certificate in at least one jurisdiction.15 years of experience in senior in-house legal leadership roles with a significant focus on global re...

DescriptionYOUR IMPACTWere looking for a professional individual who wants to apply their understanding of financial markets and be at the heart of regulatory the continued high rate of change in the regulatory reporting space Regulatory Operations professionals have the platform to significantly i...

Primary Function of PositionThis position will partner with the in-country RA team as well as the Product Localization Engineering (PLE) and other cross-functional supporting teams make sure the companys regulatory affairs activities are conducted in accordance with company policies and in complianc...

Primary Function of PositionThis position will partner with the in-country RA team as well as the Product Localization Engineering (PLE) and other cross-functional supporting teams make sure the companys regulatory affairs activities are conducted in accordance with company policies and in complianc...

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies.Responsible for managing and preparing 510(k) submissions to obtain FDA clearance to commercially di...

Responsibilities & QualificationsRESPONSIBILITIESThe SeniorIA Policy and Compliance Certified Professionalis expected to be able to accomplish the following:Capabilities reflecta strong foundationin Federal laws and regulations governing information security / privacy and information assurance and a...

Assist in ensuring compliance with current and upcoming renewable fuel regulations including the Renewable Fuel Standard (RFS) various Low Carbon Fuel Programs (LCFS) and the Canadian Clean Fuels Regulations (CFR) Assist with all aspects of Renewable Identification Number (RIN) and biofuels reportin...

The Regulatory Affairs Associate role is responsible for assisting with preparing and submitting the appropriate documentation for pre-market submissions (i.e. FDA 510(k) submissions Health Canada Device License Applications). This role also supports post-market regulatory compliance activities. Rol...

The Regulatory Affairs Engineer role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies.Responsible for managing and preparing 510(k) submissions to obtain FDA clearance to commercially dist...

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies.Responsible for managing and preparing 510(k) submissions to obtain FDA clearance to commercially di...

Career-defining. Life-changing.At iRhythm youll have the opportunity to grow your skills and your career while impacting the lives of people around the world. iRhythm is shaping a future where everyone everywhere can access the best possible cardiac health solutions. Every day we collaborate create...

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...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...