Regulatory Submissions Jobs in USA

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...

Noema Pharma is a biotech company developing groundbreaking therapies to address the most disabling symptoms in orphan conditions of the brain and nervous system. Noemas research and development is focused on understanding and meeting patient needs using our novel therapies.TasksThe Head of Clinical...

21391-1 Program Manager - Compliance Platform (Inovaare)- Healthcare domain Location: Location - Long Island CAOnsite Requirement - YesNumber of days onsite - 3 days Rate:$65-70/HR Must Have Skills -Skill 1 - Yrs of Exp - ComplainceSkill 2 - Yrs of Exp - InovaareSkill 3 - Yrs of Exp - Internal audit...

At Syngenta our goal is to build the most collaborative and trustworthy team in agriculture providing top-quality seeds and innovative crop protection solutions that improve farmers success. To support this mission Syngentas Product Safety Team is seeking a Senior Human Safety Toxicologist in Greens...

The Sr. Scientist II is reporting to the Biomaterials Research group in Tissue Material Sciences (TMS). The Sr. Scientist II will play a pivotal role in the development of innovative biomaterials for next-generation medical aesthetics products. Leveraging expertise in biomaterials polymers and biolo...

Leads the direction planning and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in and may lead cross-functional teams to generate deliver and disseminate high-quality clinical data supporting overall product scientific and busines...

Leads the direction planning and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in and may lead cross-functional teams to generate deliver and disseminate high-quality clinical data supporting overall product scientific and busines...

Oversees the direction planning execution and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in cross-functional teams to generate deliver and interpret high-quality clinical data supporting overall product scientific and business...

Oversees the direction planning execution and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in cross-functional teams to generate deliver and interpret high-quality clinical data supporting overall product scientific and business...

Oversees the direction planning execution and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in cross-functional teams to generate deliver and interpret high-quality clinical data supporting overall product scientific and business...

AbbVie Analytical Research & Development (Analytical R&D) is a global analytical scientific organization responsible for all CMC analytical activities related to the development of AbbVies pharmaceutical scope includes AbbVies diverse pipeline of innovative small molecule medicines and spans from t...

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 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...

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...

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...

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...

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 ap...