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...

This person will join our Kelly FSP (Functional Service Regulatory Affairs, Specialist, Regulatory, Technical Support, International, Business Partner, Business Services, Staffing. Kelly Science and ...

This person will join our Kelly FSP (Functional Service Regulatory Affairs, Specialist, Regulatory, Technical Support, International, Business Partner, Business Services, Staffing. Kelly Science and ...

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...

Supporting the regional Pharma division Sales Team on topics including regulatory, legal, compliance, quality and product safety. Creation and ongoing update of product regulatory information in stand...

The Regulatory Affairs Specialist is a key partner within Regulatory Affairs and will have responsibility of the direct execution of some corporate regulatory filings. The Kardion Regulatory Affairs t...

Demonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice, Good Practices training programs, SOP development, and GMP audits and inspections). Minimum five ...

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...

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 Regulatory Affairs Specialist supports the development and implementation of the global regulatory strategy for SkinMedica products. PhD degree in a scientific field, with no experience in regulat...

The Regulatory Affairs Specialist supports the development and implementation of the global regulatory strategy for SkinMedica products. Basic knowledge of personal care product industry regulatory af...

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.

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...

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...

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 ...

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 ...

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...

Participate in representing the OUS regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regula...

Minimum five (5) years of experience in Regulatory Affairs. Demonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice, Good Practices training programs, SOP...

Demonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice, Good Practices training programs, SOP development, and GMP audits and inspections). Minimum five ...

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.

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