Regulatory Affairs Associate: Average Salary in 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. ...

The Program Manager has the overall responsibility of developing, planning, managing, and implementing non-degree certificate programs and courses offered on quarterly basis for the Planning unit. Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree program...

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

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

A company is looking for a Security Program Manager to drive engagement across business and technology stakeholders in security processes. ...

A company is looking for a Project Manager for Admissions Communication. ...

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....

Chemistry; advanced degree is a plus6+ years of pharmaceutical industry experience in CMC Regulatory Affairs, with a focus on small moleculesExperience in leading high-quality CMC regulatory submissions for global marketing applicationsStrong knowledge of global regulatory guidelines (FDA, EMA, ICH)...

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...

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

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 Program Manager (Legal and Operations) to join their Legal Operations team on a remote, contract basis. ...

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

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

A company is looking for an Associate Director, Global Regulatory Project Management and Strategic Planning - GI. ...

The Project Manager I is a mid-level project management position responsible for overseeing projects from planning through completion and ensuring client satisfaction by delivering unparalleled service. Provides overall project management support for several small to medium projects or one large pro...

At Attic Projects, we are at the forefront of our industry, driving innovation and growth across our locations in San Diego, Orange County, and North & South Seattle. Our Operations Managers play a pivotal role in ensuring seamless day-to-day operations, optimizing efficiency, and upholding our ...

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 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...

The Program Manager - Clinical Quality Assurance is primarily responsible for leading the management of GCP quality activities in support of studies and projects across one or more clinical programs to drive proactive quality management, and ensure compliance with corporate policies and functional p...

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...

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 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...