Regulatory Affairs Lead Jobs in USA

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...

As we scale rapidly in North America were building a world-class Public Affairs function to shape policy strengthen our regulatory positioning and elevate our influence across government academia and leading institutions.The RoleWere seeking a North America Lead Public Affairs to serve as IFSs prima...

The Senior Associate Regulatory Affairs Submission Management manages medium to high impact moderately complex submission projects involving multiple cross-functional regulatory submission teams. With input from the submission teams this individual establishes and maintains submission content planne...

The Senior Manager RA Global Reg Strategy US & Canada - Immunology is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development. Assures that regulatory strategies defined wit...

The Senior Manager RA Global Reg Strategy US & Canada - Immunology is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development. Assures that regulatory strategies defined wit...

Remote Regulatory Affairs contractor requires: Bachelors degree in engineering life sciences regulatory affairs legal or a related field 5-10 years of global medical device regulatory experience Proven experience preparing writing and submitting FDA 510k submissions (end to end) Experience with oph...

Remote Regulatory Affairs contractor requires: Bachelors degree in engineering life sciences regulatory affairs legal or a related field 5-10 years of global medical device regulatory experience Proven experience preparing writing and submitting FDA 510k submissions (end to end) Experience with oph...

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...

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...

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...

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...

Department:107000 RegulatoryLocation:San Diego USA- RemoteBe a part of a global team that is inspired to make a difference in the lives of people living with rare disease.At Travere Therapeutics we recognize that our exceptional employees are vital to our success. We are a dedicated team focused on...

Build our future together:At Regeneron we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director to join our Regulatory Affairs Strategy team. The Director Regulatory Affairs Strategy will provide leadership on global regulatory acti...

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight aga...

HOURGLASS COSMETICS Senior Specialist Regulatory Affairs (Hybrid Role) Relocation Assistance OfferedConnected by creativity and driven by purpose. Hourglass Cosmetics is a vegan and cruelty-free beauty brand redefining luxury cosmetics with high-performance products innovative formulas and award-wi...

HOURGLASS COSMETICS Senior Specialist Regulatory Affairs (Hybrid Role) Relocation Assistance OfferedConnected by creativity and driven by purpose. Hourglass Cosmetics is a vegan and cruelty-free beauty brand redefining luxury cosmetics with high-performance products innovative formulas and award-wi...

The Vehicle Compliance & Regulatory Affairs Manager is responsible for ensuring all vehicles manufactured by Noovo comply with applicable Federal Motor Vehicle Safety Standards (FMVSS) National Highway Traffic Safety Administration (NHTSA) regulations Environmental Protection Agency (EPA) requiremen...

Primary Function of Position The Sr. Regulatory Affairs primary responsibilities include developing regulatory plans reviewing design input/output documentation identification of applicable standards and guidance documents performing regulatory assessments to determine the impact of design/process c...

Senior Regulatory Affairs Specialist Location: Mountain View CA 94043 Work Arrangement: Onsite 3 Days Per Week Position Summary The Senior Regulatory Affairs Specialist is responsible for developing regulatory plans reviewing design input/output documentation identifying applicable standards and...

1. Support regulatory submission and strategic direction for all ORICs development programs. 2. Lead to deliver high quality and timely regulatory submissions in alignment with corporate goals and in compliance with all applicable regulatory requirements.3. Coordinate and collaborate regulatory acti...