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...

Regulatory Affairs Specialist - Valencia, CA. Kelly® Science & Clinical is seeking a Regulatory Specialist for a temporary, long-term position (approx. The role ensures high-quality products are consi...

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:. Deep pract...

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 ...

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 ...

The Regulatory Affairs Specialist is a key partner within Regulatory Affairs and will have responsibility of the direct execution of some corporate regulatory filings. VP of Quality & Regulatory Affai...

The Regulatory Affairs Specialist is a key partner within Regulatory Affairs and will have responsibility of the direct execution of some corporate regulatory filings. VP of Quality & Regulatory Affai...

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 ...

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...

We are presently hiring for a **Regulatory Affairs Specialist II** to work on-site at our Cardiac Rhythm Management (CRM) location in Sylmar, CA. Reviews and evaluates communications to ensure commu...

Regulatory Affairs/Compliance Specialist. They are in search of a **Regulatory Affairs Specialis** t to play an exciting role across their innovative processes in LA!. Collaborate with teams to develo...

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...

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

The Regulatory Affairs Specialist supports the development and implementation of the global regulatory strategy for SkinMedica products. BS degree in a scientific field, plus two years’ experience in ...

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.

He/She has responsibility for compliance with US and EU regulatory requirements and partners with the international regulatory affairs group to support regulatory submissions. Minimum of 7 years of ex...

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...

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...

In this dynamic role as a Senior Regulatory Affairs Specialist, you will be responsible for informing both local and global regulatory partners of sustaining changes through the Medtronic Agile system...

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...

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...

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.