The Regulatory Affairs Senior Specialist II, NPD serves as the RA lead on New Product Development (NPD) core teams working on simple to medium complicated assay, instrument, software projects and/or s...
read moreWe are seeking a Life Sciences-Regulatory Affairs Specialist for an assignment in South San Francisco California.
We are seeking a Life Sciences-Regulatory Affairs Specialist for an assignment in South San Francisco California.
As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and compliant business processes and environ...
read moreThis **Regulatory Affairs Specialist** **II** will work out of our Pleasanton, CA location in our Heart Failure Division. Reviews and evaluates communications to ensure communications convey all n...
read moreAs an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and compliant business processes and environ...
read moreThis **Regulatory Affairs Specialist** **II** will work out of our Pleasanton, CA location in our Heart Failure Division. Prepares robust regulatory applications (either for FDA or for internation...
read moreThe Regulatory Affairs Senior Specialist II, NPD serves as the RA lead on New Product Development (NPD) core teams working on simple to medium complicated assay, instrument, software projects and/or s...
read moreAs an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and compliant business processes and environ...
read moreAs an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and compliant business processes and environ...
read moreSenior Regulatory Affairs Specialist. Support audits and regulatory inspections by preparing necessary documentation and responses. Monitor and interpret evolving regulatory requirements to guide inte...
read moreSenior Regulatory Affairs Specialist. Maintain regulatory databases and submission timelines. Collaborate with cross-functional teams to ensure adherence to regulatory standards (FDA, EU MDR, etc.
Sr Regulatory Affairs Specialist This position is based in our Campbell, California offices. In consultation with responsible Regulatory Affairs Management, interact and negotiate directly with regula...
read moreThe Principal Regulatory Affairs Specialist hired will report to the Senior Director of Regulatory and Quality, with sights to build out an RA team as needed. Assess regulatory impact of post-market c...
read moreThe Principal Regulatory Affairs Specialist hired will report to the Senior Director of Regulatory and Quality, with sights to build out an RA team as needed. Assess regulatory impact of post-market c...
read moreUltimate Staffing Services is actively seeking a dedicated Regulatory Affairs Specialist to join their client's team in Union, California. Regulatory Affairs Specialist, with at least 2 years in the m...
read moreCompile, prepare, review, and submit regulatory documents, including Device Master files, technical files, and annual reports, under the direction of the Manager, Regulatory Affairs. Ultimate Staffing...
read moreAs an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and compliant business processes and environ...
read moreAs an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and compliant business processes and environ...
read moreAs an individual contributor, the Senior Regulatory Affairs Specialist will support product development and regulatory activities to commercialize new digital products and features including generativ...
read moreAs an individual contributor, the Senior Regulatory Affairs Specialist will support product development and regulatory activities to commercialize new digital products and features including generativ...
read moreRepresents Global Regulatory Affairs at research and development meetings and presents agreed upon regulatory positions. Missed registration deadlines or inaccurate registration packages can delay reg...
read moreRepresents Global Regulatory Affairs at research and development meetings and presents agreed upon regulatory positions. A minimum of five years of experience in the Medical Products Industry in Regul...
read moreThe individual may monitor and influence changing regulations and guidance, interface with outside regulatory agencies and trade associations, develop innovative regulatory submission strategy, and pr...
read moreAs an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and compliant business processes and environ...
read moreAs an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and compliant business processes and environ...
read moreThe individual may monitor and influence changing regulations and guidance, interface with outside regulatory agencies and trade associations, develop innovative regulatory submission strategy, and pr...
read moreThis **Regulatory Affairs Specialist** **II** will work out of our Pleasanton, CA location in our Heart Failure Division. As an individual contributor, this position performs specialized level wor...
read moreThis **Regulatory Affairs Specialist** **II** will work out of our Pleasanton, CA location in our Heart Failure Division. Regulatory Affairs Professionals Society Certification is a plus. Prepares...
read moreThe individual may monitor and influence changing regulations and guidance, interface with outside regulatory agencies and trade associations, develop innovative regulatory submission strategy, and pr...
read moreThe Senior Regulatory Affairs Specialist will collaborate across teams to manage complaint reporting, support audits, and ensure compliance with EU MDR and other applicable regulatory standards. The S...
read moreThe individual may monitor and influence changing regulations and guidance, interface with outside regulatory agencies and trade associations, develop innovative regulatory submission strategy, and pr...
read moreSenior Staff Regulatory Affairs Specialist. Senior Staff Regulatory Affairs Specialist. Prepares and submits electronic and paper regulatory submissions according to applicable regulatory requirements...
read moreSenior Staff Regulatory Affairs Specialist. Senior Staff Regulatory Affairs Specialist. Assists in the development of regulatory strategy and updates strategy based upon regulatory changes.
Organize, update, and maintain regulatory documentation in accordance with department and company procedures including maintaining logs and trackers. Maintain positive and cooperative communications a...
read moreWith 5-8 years of experience, you possess deep professional know-how and experience in regulatory affairs. Candidates have a mastery of regulatory guidance documents and requirements for FDA 510(k) su...
read moreProven expertise in all aspects of Regulatory Affairs; Strategy Planning, Submission Prep, US and major market regulatory requirements, project management, and negotiations. Responsibilities also incl...
read moreProven expertise in all aspects of Regulatory Affairs; Strategy Planning, Submission Prep, US and major market regulatory requirements, project management, and negotiations. Responsibilities also incl...
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