Intern, Regulatory Affairs - Aliso Viejo, CA

+Be at the forefront of innovation – shape regulatory strategies that bring breakthrough therapies and life-changing technologies to patients around the world. · ...

Are you interested in working for an organization that is making a difference in people's lives every day? · ...

Are you interested in working for an organization that is making a difference in people's lives every day? We're a high-growth company · ...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partne ...

We are a high-growth company looking for an intern in Regulatory Affairs to join our team. · The Regulatory Affairs team is responsible for executing regulatory strategies and obtaining approvals for our products. · This internship will provide valuable experience and skills in r ...

Sr. Specialist, Regulatory Affairs · Salary Range: $91,628 - $120,263 · (Financial compensation packages may be higher/lower than listed, & will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs ...

Principal, Regulatory Affairs · Salary Range: $119,000 - $156,000 · (Financial compensation packages may be higher/lower than listed, & will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and ...

We are a high-growth company with an entrepreneurial spirit that produces reliable products supported by proven clinical data. · - Familiarize with the design manufacture and clinical use of Terumo Neuro products · - Perform specific regulatory tasks for new/modifified product · ...

Be at the forefront of innovation – shape regulatory strategies that bring breakthrough therapies and life-changing technologies to patients around the world. · ...

Principal, Regulatory Affairs · Salary Range: $119,000 - $156,000 · (Financial compensation packages may be higher/lower than listed, & will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and ...

Responsible for establishing preparing and leading the strategy for worldwide product approval submission activities As a recognized expert manage multiple large projects or processes Responsible for submission activities focused on USEUCanada and for ensuring compliance to FDA a ...

Sr. Specialist, Regulatory Affairs · Salary Range: $91,628 - $120,263 · (Financial compensation packages may be higher/lower than listed, & will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs ...

Sr. Regulatory Affairs Operations Specialist · Salary Range: $91,628 - $120,263 · (Financial compensation packages may be higher/lower than listed, & will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, busin ...

Sr. Regulatory Affairs Operations Specialist · Salary Range: $91,628 - $120,263 · (Financial compensation packages may be higher/lower than listed, & will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, busin ...

Responsible for preparing strategy for worldwide product approval submission activities focused on US/EU/Canada and ensuring compliance to FDA and international regulatory agency requirements. · As a contributing member on product development and operation teams. · ...

The job description is for a Sr. Specialist, Regulatory Affairs position at MicroVention. The role involves preparing strategy for worldwide product approval submission activities focused on US/EU/Canada and ensuring compliance to FDA and international regulatory agency requireme ...

12814BR · Title · Associate Principal, Regulatory Affairs · Job Description · Responsible for establishing and preparing strategy for worldwide product approval submission activities focused on US/EU/Canada and ensuring compliance to FDA and international regulatory agency requir ...

We are seeking a Regulatory Affairs Specialist to provide regulatory support and expertise for U.S. and global medical device submissions.This role will support execution of global regulatory strategies, ensure compliance with FDA, EU, and international requirements, and collabor ...

We are seeking a Regulatory Affairs Specialist (RAS) with strong IVD experience to support the transition from IVDD to IVDR. This role is responsible for revising and maintaining IVD technical documentation, supporting IVDR labeling conversions, and managing regulatory notificati ...

We are seeking a Regulatory Affairs Specialist to provide regulatory support and expertise for U.S. and global medical device submissions. · Provide regulatory support for U.S. and global submissions. · ...