Regulatory specialist jobs in Palo Alto, CA

A company is looking for a Senior Regulatory Specialist to support product compliance strategies and.. years of experience in Quality and Regulatory roles, particularly in medical devices or..

Regulatory Affairs Associate 6 month contract Onsite in Alameda, CA Responsibilities. Responsible for filing necessary applications and handling all government interactions pertain..

R&D to join our growing team. The Regulatory Specialist is a part of Research and Development, this team.. RESPONSIBILITIES Oversee day to day regulatory operations (formula review, filings, formula testing..

Assist in the preparation of regulatory submissions in support of IVDR implementation of Toxicology and.. Tasks include. o Organize and assist in the review of materials for inclusion in regulatory submissions..

Position Overview The Sr. Regulatory Affairs Specialist will be responsible for assisting and supporting.. This position plays a crucial role in ensuring regulatory compliance by meticulously reviewing marketing..

Clinical Regulatory Coordinator. Specialist Contract Have you got what it takes to succeed The following.. We are looking for a detail oriented clinical professional to join our growing Regulatory team as a..

A medical device client of ours in the East Bay Area is looking to bring on a Regulatory Affairs Specialist IV position! MUST BE ABLE TO COMMUTE TO EAST BAY AREA 3 DAYS A WEEK ON SITE (2 DAYS..

Program and Regulatory Specialist (Electric Generation System Program Specialist I) Salary. 9,832.00.. The Energy Commission seeks a Program and Regulatory Specialist to fill one position in the Special..

Full Time, Onsite Overview. A leading provider in the health care and digital health space is seeking a Senior Regulatory Affairs Specialist to join their regulatory team. The company focuses on..

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 Compile and maintain regulatory..

Base knowledge of global regulatory requirementsProject management skills a plusDemonstrated team.. Bachelor's degree1 3 years of experience in Regulatory AffairsSoftware medical device experience a plus..

In collaboration with the Director of Accreditation, The Accreditation and Regulatory Compliance Specialist manages all aspects of accreditation, regulatory and hospital licensure compliance..

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..

Assist in the preparation of regulatory submissions in support of IVDR implementation of Toxicology and.. Tasks include o Organize and assist in the review of materials for inclusion in regulatory submissions..

Preferred Education and Experience. 10. years of legal practice in healthcare regulatory and.. Preferred Education and Experience. 10. years of legal practice in healthcare regulatory and..

Kelly. Science & Clinical is seeking a Senior Regulatory Affairs Specialist for a 1 year contract.. Position title. Regulatory Affairs Senior Specialist, Global Market Protection Workplace. Remote Shift..

With 5 8 years of experience, you possess deep professional know how and experience in regulatory.. Candidates have a mastery of regulatory guidance documents and requirements for FDA 510(k) submissions..

The responsibilities of a Senior Regulatory Specialist in the energy sector will vary depending on the.. DUTIES AND RESPONSIBILITIES Regulatory Compliance. knowledge of federal and municipal regulations..

Job Summary & Responsibilities The Principal Regulatory Affairs Specialist will be part of this high.. Reviews and approves technical documentation.Prepare regulatory submissions such as US pre submissions..