Regulatory Affairs Associate: salario promedio en San Ramon, CA in 2024

Prepare and coordinate the compilation and/or submission of documents to regulatory agencies in supp. ...

Regulatory Affairs Associate I. A Master's Degree in Regulatory Affairs with a minimum of 3 months of regulatory experience (internship) is required. Help determine regulatory strategies for manufacturing changes and regulatory activities. Coordinate and track workflows for regulatory submissions. ...

Degree in Regulatory Affairs with a minimum of months of regulatory experience (internship) is required. Degree in Regulatory Affairs with a minimum of months of regulatory experience (internship) is required. Help determine regulatory strategies for manufacturing changes and regulatory activities. ...

The Head of CMC Regulatory Affairs / Associate Director will lead the site Regulatory Affairs function and customer related RA CMC compliance activities. Internal regulatory support for operation and control eg:Review and approval of Lonza Regulatory Intelligence Bulletin, Interpretation of EU, US a...

Bachelor’s degree in a scientific field, preferably Chemistry or Pharmacy, with 1-3 years of experience, or a Master’s Degree in Regulatory Affairs with a minimum of 3 months of regulatory experience (internship) is required. Help determine regulatory strategies for manufacturing changes and regulat...

A Bachelor’s degree in a scientific field, preferably Chemistry or Pharmacy, with - years of experience, or a Master’s Degree in Regulatory Affairs with a minimum of months of regulatory experience (internship) is required. Help determine regulatory strategies for manufacturing changes and regulator...

Assist in preparing product dossiers for regulatory submission to regulatory. Prepare and coordinate the compilation and/or submission of documents to regulatory agencies in support of maintenance and compliance requirements as well as development projects. You will be the primary contact and provid...

Regulatory Affairs Associate I. A Master’s Degree in Regulatory Affairs with a minimum of 3 months of regulatory experience (internship) is required. Help determine regulatory strategies for manufacturing changes and regulatory activities. Coordinate and track workflows for regulatory submissions. ...

During the life of a project, the Project Manager manages and supervises employees assigned to the project. The Project Manager is expected develop and maintain a client base, manage sales, and manage the field labor for each project. The Project Manager utilizes and coordinates staff from all depar...

Responsible for reporting monthly adjustments and corrections to the Compliance Manager. ...

Experience with HUD and Tax Credit program, EIV knowledge, Audit procedure, Multi layered financing experience....

Submits product labeling in compliance with legal/regulatory requirements and communicates planned/approved changes with operations, commercial, medical affairs and marketing. Has recognized regulatory expertise and extensive knowledge of regulatory requirements and regulations with ability to strat...

Director of Regulatory Affairs Body Contouring and Regulatory Innovation MPS. Directs and supports development of the regulatory strategy related to MPS activities for device regulatory activities in a variety of counties including but not limited to US, EU, US, Japan, and China. Supports regulator...

The Clinical Program Manager – Oncology, EMEA will be responsible for overseeing the execution of clinical trials in oncology and other therapeutic areas, as required. At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, inclu...

ERM has an opportunity for an experienced biologist/regulatory specialist to join our thriving global consulting firm as a. Principal Biologist/Regulatory Specialist, Power and Renewables. Principal Biologist/Regulatory Specialist. Serve as Project Biologist/Regulatory Specialist for environmental i...

Assist in the preparation of regulatory submissions in support of IVDR implementation of Toxicology and Therapeutic Drug Monitoring Assays. Organize and assist in the review of materials for inclusion in regulatory submissions both in the EU and worldwide. Support the preparation of dossiers and sub...

The Environmental Compliance Specialist is responsible for coding environmental commitments from environmental and permit approval documents into the Authority's Environmental Management and Mitigation Assessment database application (EMMA), preparing reports in EMMA to identify gaps and document mi...

Manager in Regulatory Affairs is responsible for developing and managing regulatory strategies to remain compliant with U. Extensive knowledge of regulatory requirements, including ICH and regional requirements and an understanding of current global and regional trends in regulatory affairs. FDA and...

As an individual contributor, this position performs specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for the worldwide regulatory registration, ensuring products and procedures comply with regulatory agency specifications. Prepares robust ...

As the Senior Global Regulatory Affairs Specialist, you will be responsible for regulatory activities related to the development and implementation of global regulatory strategies to support the submission, filing, and registration of multiple indications (clinical applications or “apps”) in general...

This **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 work assignments and/or analyses, evaluation, preparation, and submission of documentation for the worldwid...

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 environment. Principal Regulatory Affairs Specialist. This position performs specialized level work assignm...

Senior Manager, Medical Affairs. Medical Affairs Lead and International Business team (IBT) to execute. ...

As an International Regulatory Project Manager, you will be a member of CDx International CDx within the International Regulatory Chapter. Provide input to project and product regulatory strategy based on international regulatory requirements and support international regulatory submissions by provi...

As an International Regulatory Project Manager you will be a member of CDx International CDx within the International Regulatory Chapter. Provide input to project and product regulatory strategy based on international regulatory requirements and support international regulatory submissions by provis...