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.

20 Regulatory Affairs Specialist jobs in CA

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

$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

$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

Fremont, CA
Provides input on and reviews protocols and reports for: design verification, design validation, shelf life, pre-clinical studies, and clinical studies.
industry
Business Services
experience
Not Specified

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

Corona, CA
The Regulatory Affairs Specialist will be part of the global regulatory team responsible for formula and labeling compliance as well as product registrations worldwide. T
industry
Business Services
experience
5 - 7 years

Irvine, CA
Lead the submission of licenses and authorizations for the maintenance of existing products, international registrations, and dossiers.
industry
Biotech/Pharma
experience
5 - 7 years

Santa Clara, CA
Review product changes for impact on regulatory filings worldwide, and research regulatory issues and provide guidance and advice to colleagues. Author regulatory plan associated with the products.
industry
IT Consulting/Services
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

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

Santa Clara, CA
Collect and coordinate information and prepare regulatory documentation for submission to regulatory agencies or to commercial partners, advise on the submission strategy. Responsible for product submissions, license renewals, periodic updates and registrations to regulatory agencies.
industry
Business Services
experience
5 - 7 years

Yorba Linda, CA
With minimal supervision, provides independent regulatory guidance to product development teams in strategic planning, pre-marketing, and related submissions to support optimal timelines for new/modified product launches.
industry
Business Services
experience
Less than 5 years

Santa Ana, CA
Responsible for the Ad/Promo Regulatory review and approval of U.S. promotional and scientific materials for assigned products, and other products as determined by workload.
industry
Manufacturing / Diversified
experience
5 - 7 years

Valencia, CA
In this role, the selected candidate will support the regulatory submission activities to obtain and maintain approvals for conducting clinical investigations and for commercially distributing products worldwide.
industry
Medical Devices & Diagnostics
experience
8 - 10 years

Concord, CA
In this role, the selected candidate will ensure compliance with regulatory agency regulations and interpretations.
industry
Biotech/Pharma
experience
Less than 5 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

$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

$40K - $60K - San Jose, CA
Ability to handle multiple tasks and to prioritize/ schedule work to meet business needs with routine supervision.
industry
Medical Devices & Diagnostics
experience
Less than 5 years

Irvine, CA
Prepares regulatory labeling requirements specifications for new and modified products, and reviews product labeling to ensure compliance.
industry
Biotech/Pharma
experience
Less than 5 years