Regulatory specialist jobs in Irvine, CA

We're currently seeking a dynamic and experienced Project Manager (Medical Device Regulatory). The role.. years of experience with a successful track record in Medical Device Regulatory projects. Project..

For further detail on the spin off from Edwards Lifesciences, please consult this 2023 Investor Conference Presentation, .How you will make an impact As a Senior Specialist, Regulatory Affairs..

Description Position at Prismatik Essential Functions. Provides expertise and guidance in interpreting policies, regulatory and or governmental regulations, and internal regulations to assure..

Supervise vendor relations, including conducting initial due diligence assessments and monitoring vendor performance to uphold compliance with regulatory standards. Establish and uphold change..

As part of the continued growth and innovation of our Capital Project Delivery service offering, ERM has an opportunity for an experienced biologist regulatory specialist to join our thriving..

Job Description Position. Sr Regulatory Affairs SpecialistLocation. Sunnyvale, CaliforniaPosition Type.. Contract Date. 02 21 2023Salary. Starting at. 50.00 The Sr Regulatory Affairs Specialist is responsible..

A bit about us Medical Device Manufacturer in Irvine CA is looking for a Sr Regulatory Affairs Specialist to join their growing team!Why join us?Great pay, benefits and work life balanceJob..

Minimum five (5) years of experience in Regulatory Affairs.Knowledge and Abilities Proficient knowledge.. Demonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice..

This position is responsible for assisting in obtaining regulatory approvals and ensuring compliance to FDA and international regulatory agency requirements including ISO, local, state and or..

Job Title. Regulatory Affairs SpecialistJob Responsibilities This position is responsible for providing.. Provides guidance on regulatory requirements necessary for strategic and contingency planning, including..

The Sr. Manager, Regulatory will report to the VP, QC Regulatory and help provide leadership and.. The Sr. Manager, Regulatory will work closely with cross functional teams to help determine regulatory..

They are looking to bring no a Sr. Manager of Regulatory Affairs to play a part in their early and late.. Responsibilities. Provide leadership to the regulatory therapy area team. Manage regulatory interface..

Director, CMC Regulatory Affairs Direct Hire Full Time Role Salary Range. 208,000. 235,000 per year.. Hybrid Role Job Summary. The position is responsible for providing CMC regulatory strategies and leading..

Minimum of 15 total years of progressive related experience in regulatory affairs in the pharmaceutical.. Experience with designing and executing creative regulatory strategies for innovative products..

Regulatory Leadership. Provide regulatory guidance to project teams, collaborating with cross functional.. Lead teams in evaluating strategy options, identifying and mitigating regulatory risks, and guiding..

Real Estate Regulatory Specialist. Irvine, CA (Hybrid). 30 Months Project Job Duties. As a Real Estate.. Managing Regulatory approval requirements and ensuring compliance with all applicable regulations..