Act as a backup to Regulatory Affairs Specialist 1 and 2 in collecting and managing regulatory and technical documents from suppliers and maintaining a substantiation database. Regulatory Affairs Spec...
read moreThis person will join our Kelly FSP (Functional Service Regulatory Affairs, Specialist, Regulatory, Technical Support, International, Business Partner, Business Services, Staffing. Kelly Science and ...
read moreRegulatory 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...
read moreThe 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...
read moreThe 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...
read moreSenior Regulatory Affairs Specialist. Masters Degree in Regulatory Affairs and may be used in lieu of direct regulatory experience. Provides mentoring and leadership to Regulatory Specialist I and II ...
read moreAct as a backup to Regulatory Affairs Specialist 1 and 2 in collecting and managing regulatory and technical documents from suppliers and maintaining a substantiation database. Regulatory Affairs Spec...
read moreSenior Regulatory Affairs Specialist. Masters Degree in Regulatory Affairs and may be used in lieu of direct regulatory experience. Provides mentoring and leadership to Regulatory Specialist I and II ...
read moreThis person will join our Kelly FSP (Functional Service Regulatory Affairs, Specialist, Regulatory, Technical Support, International, Business Partner, Business Services, Staffing. Kelly Science and ...
read moreRegulatory 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...
read moreSupporting 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...
read moreSupporting 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...
read moreSeeking 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:. In-depth k...
read moreSeeking 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:. In-depth k...
read moreJob Title: Regulatory Affairs Specialist. Life Sciences, Engineering, Regulatory Affairs, or a related field. Regulatory Affairs Certification (RAC) or equivalent credential (preferred).
Job Title: Regulatory Affairs Specialist. Regulatory Affairs Certification (RAC) or equivalent credential (preferred). Life Sciences, Engineering, Regulatory Affairs, or a related field.
Job Title: Regulatory Affairs Specialist. Regulatory Affairs Certification (RAC) or equivalent credential (preferred). Life Sciences, Engineering, Regulatory Affairs, or a related field.
Job Title: Regulatory Affairs Specialist. Life Sciences, Engineering, Regulatory Affairs, or a related field. Regulatory Affairs Certification (RAC) or equivalent credential (preferred).
Job Title: Regulatory Affairs Specialist. Life Sciences, Engineering, Regulatory Affairs, or a related field. Regulatory Affairs Certification (RAC) or equivalent credential (preferred).
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...
read moreThe 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...
read moreDemonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice, Good Practices training programs, SOP development, and GMP audits and inspections). Minimum five ...
read moreDemonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice, Good Practices training programs, SOP development, and GMP audits and inspections). Minimum five ...
read moreRepresent the Regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting requirements and resolving m...
read moreIVD (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...
read moreOur location in Sylmar, CA currently has an on-site opportunity for a **Senior Regulatory Affairs Specialist** with our Cardiac Rhythm Management division. Masters Degree in Regulatory Affairs and m...
read moreRegulatory Affairs/Compliance Specialist. They are in search of a **Regulatory Affairs Specialis** t to play an exciting role across their innovative processes in LA!. Serve as the main contact for re...
read moreRegulatory Affairs Specialist/Manager will oversee medical device development and market introduction, ensuring compliance with regulatory standards for Class I, II, and III devices. Regulatory Affair...
read moreRegulatory Affairs Specialist/Manager will oversee medical device development and market introduction, ensuring compliance with regulatory standards for Class I, II, and III devices. Regulatory Affair...
read moreHe/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...
read moreHe/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...
read moreSeeking 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...
read moreThe 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...
read moreRepresent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and ...
read moreRepresent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and ...
read moreParticipate in representing the OUS regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regula...
read moreMinimum 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...
read moreMinimum 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.