Public affairs specialist jobs in Laguna Niguel, CA

Advanced degree may offset medical device industry experience. Minimum of three (3) years of Medical device industry experience. Minimum one (1) year Regulatory Affairs Experience. Ability to..

We are currently looking for a QA Specialist to work for an Orange County area contract manufacturing company. Pay Rate. 25 35 hour depending on experience. Summary. Review GMP technical..

JCW is working on an exciting search for Regulatory Affairs Specialist III for global Biotech who is.. Bachelor's degree in life sciences or a related field 4. years of Regulatory Affairs experience in the..

Job Description. Regulatory Affairs Specialist Position. Regulatory Affairs Specialist Employment Type.. Provide consultation and advice to regulatory specialists regarding change control and product..

1917BR. Title. Specialist I, Regulatory Affairs. Job Description. This position is responsible for.. Desired Qualifications. 1. Minimum one (1) year Regulatory Affairs Experience. 2. Leadership skills. 3..

About the Role As the Senior Global Regulatory Affairs Specialist, you will be responsible for.. Managing and driving all aspects of international regulatory affairs from creation to submission of..

R&D Partners is seeking to hire a Regulatory Affairs Specialist II in Lake Forest, CA.Your main responsibilities as a Regulatory Affairs Specialist II Work with global partners and support..

Medical manufacturer is hiring a Regulatory Affairs Specialist on a temporary basis. This is a 6 month.. Previous medical device experience in a Regulatory Affairs capacity. Previous experience registering..

Position Requirements Minimum two years of experience in Regulatory Affairs or Quality Assurance in the medical device industryMinimum one year of active experience applying design..

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..

We're seeking a seasoned Senior Clinical Affairs Manager to lead and oversee clinical strategy and.. Masters 8. years of experience in clinical affairs within the medical device industry, with a focus on..

Summary. We are seeking a Clinical Project Assistant (CPA) of Clinical Affairs to join our team at.. Essential Duties & Responsibilities. Support the Clinical Affairs team to execute tasks throughout the..

We are supporting a small growing biotech in the Bay Area looking for a Senior Regulatory Affairs Associate! Education, Experience and Qualification Requirements. Bachelor's Degree in a..

Job Title. Medical Affairs Consultant I Duties. The Medical Information Specialist contractor candidate.. As a medical information product specialist, perform the following duties for assigned molecules..

Role. Regulatory Affairs Project Leader Location. Santa Clara, CA Duration. 12 Months Shift Timings. 8 am to 5 pm Job Description. Education. Bachelor's degree required, Masters degree preferred..

My client is seeking a Director, Regulatory Affairs to join their Regulatory team. Responsibilities Lead.. years of Regulatory Affairs experience Advanced scientific degree preferred Extensive global pediatric..

Regulatory Affairs Manager. Permanent. San Francisco Bay Area Proclinical is seeking a Manager.. Proclinical is a specialist employment agency and recruitment business, providing job opportunities..

Our client is looking for a VP of Clinical Affairs with a specialty in heart failure to lead on their.. Requirements. Executive level experience in clinical affairs. RA or QA experience is nice to have..

Senior Director, Regulatory Affairs (Generalist) Remote Position for West Coast based candidates.. This position will be reporting into the SVP of Regulatory Affairs and will be supporting Clinical..

We are seeking an experienced and detail oriented Senior Regulatory Specialist to work on a core project.. advanced degree preferred. Minimum of 5 7 years of experience in regulatory affairs within the medical..