Essential Requirements Checklists, Design Dossiers, Technical Files and De Regulatory, Remote, Neuro, Principal, Specialist, Technical, Manufacturing, Education.

The Honest Company is on the lookout for a dedicated Regulatory Affairs Specialist to champion our mission of transparency and trust. Maintain regulatory archives and product registration databases. R...

The Honest Company is on the lookout for a dedicated Regulatory Affairs Specialist to champion our mission of transparency and trust. Maintain regulatory archives and product registration databases. R...

Seeking a Principal Regulatory Affairs Specialist to support the Kindeva business in maintaining regulatory compliance of existing manufactured products for customers on a global basis by:. Membership...

The Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and execution; collaborate with Product Regulatory ...

Provide guidance on regulatory requirements necessary for strategic and contingency planning, including developing the preliminary regulatory strategic plans. Represent the Regulatory function on manu...

Seeking a Principal Regulatory Affairs Specialist to support the Kindeva business in maintaining regulatory compliance of existing manufactured products for customers on a global basis by:. Deep pract...

The Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and execution; collaborate with Product Regulatory ...

Regulatory Affairs Specialist (Global)**. Regulatory Affairs Specialist (Global) to help expand portfolio. Strong proven hands-on regulatory affairs experience with APIs.

The Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and execution; collaborate with Product Regulatory ...

The Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and execution; collaborate with Product Regulatory ...

The Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and execution; collaborate with Product Regulatory ...

You will primarily focus on developing and refining fit-for-purpose regulatory strategies to support the digital health innovations of the Diabetes business in early phases of development with stakeho...

The Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and execution; collaborate with Product Regulatory ...

Partner with Geography RA to plan, develop and execute global regulatory activities necessary to obtain and maintain regulatory approvals in International markets (such as Canada, LATAM, EMEA). Provid...

Partner with Geography RA to plan, develop and execute global regulatory activities necessary to obtain and maintain regulatory approvals in International markets (such as Canada, LATAM, EMEA). Provid...

The Principal Regulatory Affairs Specialist is responsible for participating on product development projects, evaluating document change orders for RA assessment, drafting regulatory submissions, and ...

The Principal Regulatory Affairs Specialist is responsible for participating on product development projects, evaluating document change orders for RA assessment, drafting regulatory submissions, and ...

We are presently hiring for a **Regulatory Affairs Specialist II** to work on-site at our Cardiac Rhythm Management (CRM) location in Sylmar, CA. Certification is a plus (such as RAC from the Regula...

We are presently hiring for a **Regulatory Affairs Specialist II** to work on-site at our Cardiac Rhythm Management (CRM) location in Sylmar, CA. Acts as core team member providing review and analys...

Masters Degree in Regulatory Affairs and may be used in lieu of direct regulatory experience. Our location in Sylmar, CA currently has an on-site opportunity for a **Senior Regulatory Affairs Special...

IVD (In-vitro Diagnostics) is highly preferred.Support the IVDR project by revising the assigned technical files.Each technical file must be generated using the latest technical file template and it m...

The Regulatory Affairs Specialist creates, evaluates, and completes regulatory tasks related to the following: worldwide product registration submissions, facility registrations, technical files, FDA ...

The Regulatory Affairs Specialist III, will provide administrative and technical support to regulatory affairs leadership in order to facilitate compliance with U. The Regulatory Affairs Specialist pr...

Seeking a Principal Regulatory Affairs Specialist to support the Kindeva business in maintaining regulatory compliance of existing manufactured products for customers on a global basis by:. Participat...

Seeking a Principal Regulatory Affairs Specialist to support the Kindeva business in maintaining regulatory compliance of existing manufactured products for customers on a global basis by:. Participat...

This position is responsible for handling time sensitive Regulatory documents in accordance with appropriate regulatory agencies and internal company procedures. Assist Regulatory Management with prod...

Master's Degree in Regulatory Affairs and may be used in lieu of direct regulatory experience. Senior Regulatory Affairs Specialist. Provides mentoring and leadership to Regulatory Specialist I and II...

Senior Regulatory Affairs Specialist. Master’s Degree in Regulatory Affairs and may be used in lieu of direct regulatory experience. Certification is a plus (such as RAC from the Regulatory Affairs Pr...

Regulatory Affairs Specialist/Manager will oversee medical device development and market introduction, ensuring compliance with regulatory standards for Class I, II, and III devices. A minimum of 5 ye...

The Regulatory Affairs Specialist supports the development and implementation of the global regulatory strategy for SkinMedica products. MS degree in a scientific field, plus one year experience in re...

Minimum of 7 years of experience medical device regulatory affairs Or advanced degree with a minimum of 5 years of experience medical device regulatory affairs. He/She has responsibility for complianc...

Seeking a Senior Regulatory Affairs Specialist with expertise in US and EU regulatory requirements, EU MDR regulation, and medical device regulatory submissions to sustain the current product portfoli...

Seeking a Senior Regulatory Affairs Specialist with expertise in US and EU regulatory requirements, EU MDR regulation, and medical device regulatory submissions to sustain the current product portfoli...

The role of the Regulatory Affairs Specialist will be to support the global regulatory affairs of the business with a specialized focus on the United States. This position will be primarily responsibl...

From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and international regulatory environments. Represent the regulatory function on ...

Bachelor’s degree in Engineering, Physical or Biological Sciences, Regulatory, other technical disciplines, or equivalent.

Minimum two years of experience in Regulatory Affairs or Quality Assurance in the medical device industry.

The Sr Regulatory Affairs Specialist is responsible for ensuring digital medical device regulatory clearance to enable market access by demonstrating compliance to applicable regulations through a reg...