Regulatory Affairs Director: Average Salary in Orange, CA in 2024

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

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...

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

The Director Regulatory Affairs, Strategic Labeling is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executing multidivisional initiatives for labeling activities for drugs, devices and combination products in assigned therapeutic area(s). E...

Operate as the primary point of contact for Quality and Regulatory Affairs representation for DH product development and maintenance of marketed products and will oversee the end-to-end Regulatory Affairs and Quality strategies for DH products. DIRECTOR, QUALITY AND REGULATORY AFFAIRS, DIGITAL HEALT...

Operate as the primary point of contact for Quality and Regulatory Affairs representation for DH product development and maintenance of marketed products and will oversee the end-to-end Regulatory Affairs and Quality strategies for DH products. DIRECTOR, QUALITY AND REGULATORY AFFAIRS, DIGITAL HEALT...

The Director Regulatory Affairs Global Regulatory Lead, Global Regulatory Strategy, is responsible for developing and implementing global strategies to secure and maintain market approval for product(s) in the assigned therapeutic area. May lead the Labeling Regulatory Strategy Team (LRST), and serv...

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...

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...

Executive Director, of College Advancement. The Executive Director of College Advancement is a management position that includes. Executive Wing as part of the Office of the President. Provides regular updates to the investment and executive committees on financial standing, portfolio levels, and do...

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 Section 508 Compliance Specialist to ensure digital accessibility and compliance with federal standards. ...

A company is looking for a Project Compliance Specialist. ...

A company is looking for a Regulatory Compliance Specialist 4 to support and implement audit programs for cloud infrastructure. ...

A company is looking for a Security Technical Program Manager to lead and manage security-related programs and projects remotely. ...

A company is looking for a Senior Medicare Communications Compliance Specialist to support regulatory requirements associated with Medicare materials and sales compliance. ...

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 Senior Regulatory Compliance Specialist to assist with the implementation and maintenance of its Compliance Software Program. ...

A company is looking for an Executive Director of Investigations to lead and manage investigations into potential non-compliance with laws and company policies. ...

Global Regulatory Affairs Strategy roles (U. Responsible for supporting teams & efforts around major filing activities & Regulatory Health Authority (RHA) interactions & meetings, attending & providing regulatory support to other departments, project teams & committees. Assist Re...

The Manager Regulatory Affairs represents US regulatory affairs for device development projects. Executes US regulatory strategic plans and provides guidance to Global Regulatory Lead (GRL) and project team. Plans and prepares complex regulatory submission documents primarily for US regulatory filin...

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...

Regulatory Affairs Specialist creates, evaluates, and completes regulatory tasks related to the following: worldwide product registration submissions, facility registrations, technical files, FDA submissions, special projects, and strategy to drive market growth worldwide. Regulatory Affairs Special...

Principal, Geologist Engineer/Program Manager - ( 240003IO ). We are currently seeking a Program Manager to join the Environmental Services team in our Southern California Area. Develop, maintain, and execute program management plan, including preparing forecasts of program revenue. Regular full-tim...