Regulatory Affairs Specialist: Average Salary in Bothell, WA in 2024

The Principal Regulatory Affairs Specialist will play a critical role in preparing comprehensive regulatory strategies for complex new devices and post market changes within Philips' Ultrasound business. Develop regulatory strategies and communicate risks within regulatory strategies vs project plan...

A company is looking for a Principal Regulatory Affairs Specialist for Digital Health Apps. ...

A BS/MS in life sciences coupled with at least 3 years of experience in regulatory affairs. Preferred certification in regulatory affairs. Represent or lead Regulatory Affairs within project teams throughout the product lifecycle. Required experience in regulatory submissions (pre-submissions, EUA, ...

We’re looking for a detail-oriented professional with substantial experience in regulatory affairs, particularly concerning in-vitro diagnostic (IVD) products. Your ability to stay updated with evolving regulatory landscapes, manage multiple projects, and work closely with regulatory bodies is key t...

Regulatory Affairs Specialist - Clinical Research - Swedish Cherry Hill. This includes preparation of all submissions to the IRB to assure the protection of human subjects in research; FDA-required submissions which may include investigator 1572 forms, investigational new drug applications, device s...

Senior Regulatory Affairs Specialist. Responsible for influencing department regulatory processes and procedures, developing strategies for worldwide regulatory approval, preparing US and EU submissions, and ensuring timely and high-quality execution of all regulatory deliverables. Serve as RA Repre...

The Principal Regulatory Affairs Specialist will play a critical role in preparing comprehensive regulatory strategies for complex new devices and post market changes within Philips’ Ultrasound business. Develop regulatory strategies and communicate risks within regulatory strategies vs project plan...

The Principal Regulatory Affairs Specialist will play a critical role in preparing comprehensive regulatory strategies for complex new devices and post market changes within Philips’ Ultrasound business. Develop regulatory strategies and communicate risks within regulatory strategies vs project plan...

Job TitleSenior Regulatory Affairs SpecialistJob Description. Responsible for influencing department regulatory processes and procedures, developing strategies for worldwide regulatory approval, preparing US and EU submissions, and ensuring timely and high-quality execution of all regulatory deliver...

As part of the Medical Regulatory Affairs team, you will work with the team to maintain medical devices on the market and ensure ongoing compliance. Assist in the development of regulatory strategy and updates strategy based upon regulatory changes. Prepare and submit electronic and paper regulatory...

Senior Regulatory Affairs Specialist. Responsible for influencing department regulatory processes and procedures, developing strategies for worldwide regulatory approval, preparing US and EU submissions, and ensuring timely and high-quality execution of all regulatory deliverables. Serve as RA Repre...

Senior Regulatory Affairs Specialist (Hybrid). Senior Regulatory Affairs Associate. As part of the Medical Regulatory Affairs team, you will work with the team to maintain medical devices on the market and ensure ongoing compliance. Assist in the development of regulatory strategy and updates strate...

The Senior, Regulatory Affairs Specialist is responsible for acting as the regulatory representative on product development teams aiming to achieve and maintain regulatory compliance for NanoStrings products, with a particular focus on instrument/software development and manufacturing. Maintain Regu...

We are currently seeking an Regulatory Affairs Associate to join our Medical Division, Hybrid, to be based in Redmond, Washington. As part of the Medical Regulatory Affairs team, you will work with the team to maintain medical devices on the market and ensure ongoing compliance. Prepare and submit e...

Regulatory Affairs Specialist - Clinical Research - Swedish Cherry Hill. This includes preparation of all submissions to the IRB to assure the protection of human subjects in research; FDA-required submissions which may include investigator forms, investigational new drug applications, device submis...

As part of the Medical Regulatory Affairs team, you will work with the team to maintain medical devices on the market and ensure ongoing compliance. Prepare and submit electronic and paper regulatory submissions according to applicable regulatory requirements and guidelines for required products. Co...

The Principal Regulatory Affairs Specialist will play a critical role in preparing comprehensive regulatory strategies for complex new devices and post market changes within Philips’ Ultrasound business. Develop regulatory strategies and communicate risks within regulatory strategies vs project plan...

Regulatory Affairs Specialist - Clinical Research - Swedish Cherry Hill. This includes preparation of all submissions to the IRB to assure the protection of human subjects in research; FDA-required submissions which may include investigator 1572 forms, investigational new drug applications, device s...

As part of the Medical Regulatory Affairs team, you will work with the team to maintain medical devices on the market and ensure ongoing compliance. Assist in the development of regulatory strategy and updates strategy based upon regulatory changes. Prepare and submit electronic and paper regulatory...

Regulatory Affairs Specialist - Bothell, WA. Master’s Degree in Biomedical Regulatory Affairs, Biotechnology, or a related field and one (1) year of experience in position offered or related position including one (1) year of experience working in a medical device industry. Lead efforts in the prepa...