Public affairs specialist jobs in Palo Alto, CA
Regulatory Affairs Specialist
Job Description. Regulatory Affairs Specialist Position. Regulatory Affairs Specialist Employment Type.. Provide consultation and advice to regulatory specialists regarding change control and product..
Executive Director, U.S. Public Affairs
Executive Director, U.S. Public Affairs United States. California. Foster CityUnited States. New Jersey.. Executive Director, U.S. Public Affairs Gilead recognizes the development of innovative medicines for..
Regulatory Affairs Specialist
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..
Regulatory Affairs Specialist
Job Title. Regulatory Affairs Specialist Location. Fermont, CA Duration. 12 months Pay rate. 35 40 hr Job Description. A Day in the Life. Assist in the preparation of regulatory submissions in..
QC Specialist
We are currently looking for a QC Specialist to work for an Orange County area medical device company. Pay Rate. 25 35 hour Responsibilities. Perform visual, dimensional, and functional..
Regulator Affairs Specialist
Senior Regulatory Affairs Specialist I Overview. The Regulatory Affairs Senior Specialist I, NPD is.. Regulatory Compliance. Work with the Technical Publications team to publish regulatory compliant..
Senior Regulatory Affairs Specialist
Kelly Science & Clinical is seeking a Senior Regulatory Specialist for a 6 contract opportunity with a.. Position Title. Senior Regulatory Affairs Associate, Product Development Position Type. 6 month contract..
Senior Regulatory Affairs Specialist
Position Overview The Sr. Regulatory Affairs Specialist will be responsible for assisting and supporting.. including digital content, print media, and public relations messages, to ensure compliance with FDA..
Regulatory Affairs Specialist
Assist in the preparation of regulatory submissions in support of IVDR implementation of Toxicology and Therapeutic Drug Monitoring Assays. Tasks include. o Organize and assist in..
Regulatory Affairs Specialist
HEALTH. Guardant Health, Inc. in Palo Alto, CA seeks Regulatory Affairs Specialist. Examine, evaluate & investigate eligibility for or conformity with laws & regulations & perform other..
Regulatory Affairs Specialist
Regulatory Affairs Senior Specialist, Global Market Protection Location. Remote Shift. M F, standard.. 7 50 hr 1 year contract role Overview. The Regulatory Affairs Senior Specialist is responsible for..
Regulatory Affairs Specialist
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..
Senior Regulatory Affairs Specialist (hybrid)
We are hiring a Senior Regulatory Affairs Specialist for our Diagnostics Regulatory Affairs team who.. Review of product labeling, materials for publication, literature and Web site for accuracy, consistency..
Staff/Principal Regulatory Affairs Specialist
The Staff Principal Regulatory Affairs Specialist will function as a subject matter expert and will be.. Advanced degree preferred. Certification is a plus (such as RAC from the Regulatory Affairs..
Executive Director, U.S. Public Affairs
Executive Director, U.S. Public AffairsGilead recognizes the development of innovative medicines for.. Public Affairs team. This role is responsible for setting and executing the public affairs strategy for..
Regulatory Affairs Specialist
Assist in the preparation of regulatory submissions in support of IVDR implementation of Toxicology and Therapeutic Drug Monitoring Assays. Tasks include o Organize and assist in ..
Principal Regulatory Affairs Specialist
Job Summary & Responsibilities The Principal Regulatory Affairs Specialist will be part of this high performance team and responsible for developing regulatory strategies, preparing U.S..
Senior Regulatory Affairs Specialist
Experience. With 5 8 years of experience, you possess deep professional know how and experience in regulatory affairs. Candidates have a mastery of regulatory guidance documents and requirements..