As a Regulatory Affairs Specialist, you will play a critical role in ensuring our products meet the highest standards of compliance and safety. Apply today to join our team as a Regulatory Affairs Spe...

As a Regulatory Affairs Specialist, you will play a critical role in ensuring our products meet the highest standards of compliance and safety. Apply today to join our team as a Regulatory Affairs Spe...

The Senior Regulatory Affairs Specialist will be a part of the Neuromodulation Regulatory Affairs team. Assists with Regulatory Affairs training to cross-functional groups. Regulatory Affairs or relat...

The Senior Regulatory Affairs Specialist will be a part of the Neuromodulation Regulatory Affairs team. Assists with Regulatory Affairs training to cross-functional groups. Regulatory Affairs or relat...

Regulatory Affairs Specialist- Medical Device (IVDR). Regulatory affairs, Quality Assurance, or Manufacturing in Medical Device. Thorough knowledge of policies, practices and procedures related to Reg...

Regulatory Affairs Specialist- Medical Device (IVDR). Regulatory affairs, Quality Assurance, or Manufacturing in Medical Device. Thorough knowledge of policies, practices and procedures related to Reg...

Regulatory Affairs Specialist II.

Regulatory Affairs & QA Specialist. As a Regulatory Affairs & Quality Assurance Specialist, you’ll play a pivotal role in upholding our commitment to excellence and delivering products that our custom...

Regulatory Affairs & QA Specialist. As a Regulatory Affairs & Quality Assurance Specialist, you’ll play a pivotal role in upholding our commitment to excellence and delivering products that our custom...

Regulatory Affairs Specialist II.

The Senior Regulatory Affairs Specialist will be a part of the Neuromodulation Regulatory Affairs team. Assists with Regulatory Affairs training to cross functional groups. Regulatory Affairs or relat...

Regulatory specialist, you will develop and implement medical device regulatory strategies to obtain timely approvals from worldwide regulatory bodies. Prepare, review, and submit and provide regulato...

Regulatory specialist, you will develop and implement medical device regulatory strategies to obtain timely approvals from worldwide regulatory bodies. Prepare, review, and submit and provide regulato...

The Principal Regulatory Affairs Specialist will develop and implement regulatory strategies to obtain timely approvals from regulatory authorities worldwide. The Principal Regulatory Affairs Speciali...

Represent the Regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting requirements and resolving m...

The Principal Regulatory Affairs Specialist will develop and implement regulatory strategies to obtain timely approvals from regulatory authorities worldwide. The Principal Regulatory Affairs Speciali...

The Senior Regulatory Affairs Specialist overseeing advertising and promotional Regulatory responsibilities, works closely and partners with internal departments to efficiently and effectively meet as...

Represent the Regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting requirements and resolving m...

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 Senior Regulatory Affairs Specialist will be a part of the Neuromodulation Regulatory Affairs team. Assists with Regulatory Affairs training to cross functional groups. Regulatory Affairs or relat...

The Senior Regulatory Affairs Specialist overseeing advertising and promotional Regulatory responsibilities, works closely and partners with internal departments to efficiently and effectively meet as...

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...

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...

The Regulatory Affairs Specialist II will be a part of the Neuromodulation Regulatory Affairs team and will support the regulatory submission activities to obtain and maintain approvals for conducting...

Support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact all Bio-Rad products currently CE Marked under the IVD Directive.Activities include preparation revision o...

Support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact all Bio-Rad products currently CE Marked under the IVD Directive.Activities include preparation revision ...

Support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact all Bio-Rad products currently CE Marked under the IVD Directive.Activities include preparation revision ...

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...

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...

Regulatory Affairs Specialist - Valencia, CA. Kelly® Science & Clinical is seeking a Regulatory Specialist for a temporary, long-term position (approx. The Regulatory Specialist will also act as a bac...

Regulatory Affairs Specialist - Valencia, CA. The role ensures high-quality products are consistently delivered on time by handling regulatory submissions, CAPAs, customer complaints, conducting regul...

Thorough knowledge of policies, practices and procedures related to Regulatory Affairs. Reg Affairs, QA, R&D, Manufacturing, and/or Project Management within the IVD industry.

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...

A minimum of a bachelor’s degree and 1-3 years’ work experience in regulatory affairs. RA certification (by Regulatory Affairs Professional Society). Support the regulatory submission activities to ob...

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 ...

Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and ...

As a Specialist, Regulatory Affairs for TMTT, you will complete and maintain clinical and commercial regulatory approvals of Class III implantable products in the US and EU, focusing on the paradigm s...

As a Specialist, Regulatory Affairs for TMTT, you will complete and maintain clinical and commercial regulatory approvals of Class III implantable products in the US and EU, focusing on the paradigm s...