Regulatory Affairs Associate: salario promedio en Irvine, CA in 2024

The Regulatory Affairs Specialist supports the development and implementation of the global regulatory strategy for several products. Reviews product labeling for accuracy and for other legal/regulatory requirements and communicates planned/approved changes with other functions, including but not li...

Bachelor’s degree in Engineering, Physical or Biological Sciences, Regulatory, other technical disciplines, or equivalent. ...

Under the direction of the appropriate level manager or administrator, the Accessibility and Compliance Instructional Support Specialist performs a variety of specialized duties involved in identifying and recommending potential solutions for accessibility barriers based on current applicable guidel...

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...

A company is looking for a Section 508 Compliance Specialist to ensure digital accessibility and compliance with federal standards. ...

A company is looking for a Junior Program Manager to provide project control and contract administration for a large, diversified team. ...

Key Responsibilities:Develop and implement regulatory strategies for global medical device clearances and approvalsManage regulatory submissions and communications with FDA and EU notified bodiesProvide regulatory guidance to cross-functional teams throughout the product lifecycleRequired Qualificat...

Manager, Regulatory Affairs III to provide strategic direction and operational support for CMC regulatory activities. ...

A company is looking for a Food Regulatory Specialist to join their team remotely. Food Science, Biology, Chemistry, Toxicology, Nutrition preferred)Regulatory experience in the food industry6 months to 5 years of experience in Regulatory Affairs of a Consumer Products CompanyWorking knowledge of U....

A company is looking for a Senior Ethics and Compliance Specialist to join their Corporate Compliance team. ...

A company is looking for a Regulatory Affairs and Compliance Director (Remote). ...

A company is looking for a Manager, Project Training to assist with client-specific initiatives in the biotechnology sector. ...

A company is looking for a Senior Associate, Regulatory Operations. ...

A company is looking for a Senior Regulatory Specialist to support product compliance strategies and ensure regulatory standards are met. ...

A company is looking for an Assistant Project Manager to support the Industrial & Agriculture team with project processing and management. ...

A company is looking for a Regulatory Consulting Associate responsible for preparing plan documents and providing regulatory compliance support. ...

Director, Regulatory Affairs, Immunology. A company is looking for a Director / Sr. ...

A company is looking for a Revenue Cycle Optimization Program Manager - Reporting & Data Analytics. ...

A company is looking for a Learning Program Manager to support the training and development of their customer-facing organization. ...

A company is looking for a Project Manager for Cloud Modernization. ...

A company is looking for a Regulatory Affairs Specialist to support US and OUS regulatory activities for Class II and III products. CFR 820, MDR)Experience in regulatory affairs, clinical affairs, Quality, or Engineering is required. ...

A company is looking for a Compliance Specialist - Contractor to maintain its compliance programs. Key Responsibilities:Maintain the company's SOC 2 compliance programAssist in the preparation for and execution of SOC 2 auditsSupport the implementation of controls for StateRAMP complianceRequired Qu...

In Vitro Diagnostic Regulatory Specialist (R&D/QA). Regulatory affairs, in Quality Assurance, (R&D), Manufacturing, Project Management in IVDR (Vitro Diagnostic Regulation). ...

Director, Safety, Regulatory and Medical Affairs Quality Standards is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA) and Medical Affairs (MA) QA team which provides independent quality oversight of GxP activities, covering the AbbVie drug, device and cosmetic portfol...

The Sr Manager Regulatory Affairs represents US regulatory affairs for device development projects. Plans and prepares (or oversees) complex regulatory submission documents primarily for US regulatory filings, ensures technical accuracy, and regulatory compliance. Responsible for development, commun...