Job Market Guide: Regulatory Affairs Specialist jobs in CA

Competition
Desired Skills
Years of Experience
Years of Experience distribution graph for Regulatory Affairs Specialists in CA. Regulatory Affairs Specialists in CA have between ${} and ${} years of experience, averaging $${} years of experience.

13 Regulatory Affairs Specialist jobs in CA

San Diego, CA
Review and approve new product development documents, including but not limited to test protocols and reports, risk analysis documents, clinical protocols.
industry
Manufacturing / Diversified
experience
5 - 7 years

Carlsbad, CA
The Regulatory Specialist 4 is a core team member on product development teams. The Regulatory Specialist 4 will provide regulatory guidance by creating detailed written regulatory plans based on the Marketing Product Launch Plan for initial domestic and international product launch.
industry
Manufacturing / Diversified
experience
5 - 7 years

$100K - $120K - San Diego, CA
Draft, assemble, and file original documentation and submission materials for new or existing products to regulatory authorities to assure that all submissions are accurate, of high quality and well supported by literature and regulatory foundations, are presented in a manner to facilitate review, and are in conformance with appropriate statutes, regulations, and guidelines.
industry
Medical Devices & Diagnostics
experience
5 - 7 years

$50K - $80K - San Jose, CA
Provides metrics for regulatory management reporting and helps to identify areas for further monitoring for global product development system (GPDS) improvements.
industry
Medical Devices & Diagnostics
experience
Less than 5 years

Tustin, CA
Executing regulatory requirements in each country based on approved strategies (Europe, Middle East, Africa, Asia Pacific & Latin America)
industry
Business Services
experience
5 - 7 years

Santa Clara, CA
Participate in new product design and development project teams as regulatory affairs representative; ensure all regulatory requirements are met throughout the development process as per FDA QSR, ISO 13485, China FDA, Japan PMDA and Rest of the world regulations.
industry
Life Sciences & Research
experience
5 - 7 years

Dublin, CA
Provide regulatory marketing collateral guidance, review and approval for assigned products taking into account cleared/approved product claims.
industry
Optics
experience
5 - 7 years

$100K - $120K - San Francisco, CA
Draft, assemble, and file original documentation and submission materials for new or existing products to regulatory authorities to assure that all submissions are accurate, of high quality and well supported by literature and regulatory foundations, are presented in a manner to facilitate review, and are in conformance with appropriate statutes, regulations, and guidelines.
industry
Medical Devices & Diagnostics
experience
5 - 7 years

Irvine, CA
Responsible for regulatory review for claims support of promotional material, labeling content, product and process changes, and product documentation.
industry
Business Services
experience
5 - 7 years

Corona, CA
Coordination with external parties ( distributors, vendors, legal counsel, importers, authorities ) to ensure that products are legally compliant and any required product registrations are valid.
industry
Business Services
experience
5 - 7 years

Glendora, CA
Plans and prepares regulatory submission documents for US or OUS regulatory filings under minimal supervision.
industry
Business Services
experience
5 - 7 years

$100K - $120K - Los Angeles, CA
Draft, assemble, and file original documentation and submission materials for new or existing products to regulatory authorities to assure that all submissions are accurate, of high quality and well supported by literature and regulatory foundations, are presented in a manner to facilitate review, and are in conformance with appropriate statutes, regulations, and guidelines.
industry
Medical Devices & Diagnostics
experience
5 - 7 years

San Diego, CA
Participate in cross-functional teams by working closely with product development engineering, marketing, clinical, and quality functions.
industry
Business Services
experience
5 - 7 years