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.

22 Regulatory Affairs Specialist jobs in CA

San Diego, CA
In this role, you will communicate and interact directly with regulatory bodies and local health agencies such as US FDA to ensure adequate and appropriate information is provided as well as driving submissions to approval as effectively as possible.
industry
Medical Devices & Diagnostics
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

Valencia, CA
In this role, you will participate in the review and submission activities ( annual reports, change notifications, etc. ) to support the maintenance of marketing approvals.
industry
Medical Devices & Diagnostics
experience
5 - 7 years

Santa Clara, CA
In this role, you will support product engineering and manufacturing teams on regulatory issues, including review of design input, risk management and test documentation.
industry
Patient Care
experience
8 - 10 years

Fremont, CA
Responsible for the coordination and preparation of document packages for regulatory submissions in one or more of the following geographic regions: United States, Europe, Japan, Canada, and Intercontinental.
industry
Business Services
experience
Not Specified

Sunnyvale, CA
In this role, you will coordinate, prepare, or review regulatory submissions for Latin America projects.
industry
Patient Care
experience
5 - 7 years

Sunnyvale, CA
In this role, you will support product engineering and manufacturing teams on regulatory issues, including review of design input, risk management and test documentation.
industry
Patient Care
experience
8 - 10 years

Sunnyvale, CA
In this role, you will work independently as well as with teams to obtain and maintain global regulatory approvals for commercial distribution of products.
industry
Medical Devices & Diagnostics
experience
8 - 10 years

Carlsbad, CA
In this role you will be responsible for driving key initiatives to clean existing SKU data and create tools, processes and mechanisms for maintaining clean SKU data over time.
industry
Biotech/Pharma
experience
Less than 5 years

Santa Clara, CA
In this role, you will continue to revisit and compare regulatory outcomes with initial product concepts to make recommendations on future actions.
industry
Biotech/Pharma
experience
Less than 5 years

San Diego, CA
Participate in New Product Development cross-functional teams as the RA core team member.
industry
Energy & Environmental Services
experience
Less than 5 years

Irvine, CA
In this role, you will gather of information and research used to provide guidance and feedback to business unit regulatory teams on registration requirements for new and renewal registrations, product and process changes, and review of labeling content and guidance on process improvement projects, based on prior experience and responses from affiliates.
industry
Healthcare IT
experience
5 - 7 years

Santa Ana, CA
Demonstrate knowledge of and help ensures compliance with AMO/Abbott policies and procedures related to marketing and scientific activities supporting AMO products.
industry
Biotech/Pharma
experience
5 - 7 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

Corona, CA
In this role, you will be responsible for keeping up and understand the regulatory environment and interpretation of regulations for food and dietary supplement and how our products are affected.
industry
Business Services
experience
5 - 7 years

Santa Clara, CA
In this role, you will coordinate, prepare, or review regulatory submissions for Latin America projects.
industry
Patient Care
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

Alameda, CA
Assist in the development of regional regulatory strategy and update strategy based upon regulatory changes.
industry
Biotech/Pharma
experience
Less than 5 years

Los Angeles, CA
Support the regulatory submission activities to obtain and maintain approvals for conducting clinical investigations and for commercially distributing products worldwide.
industry
Consulting
experience
5 - 7 years

$40K - $80K - San Jose, CA
In this role, you will be responsible for the preparation and documentation of regulatory submissions to government agencies; works on problems of diverse scope where analysis of situations or data requires a review of identifiable factors.
industry
Life Sciences & Research
experience
Less than 5 years

Irvine, CA
In this role, you will be 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

San Diego, CA
In this role, you will participate and provide regulatory strategy in product design control teams.
industry
Medical Equipment
experience
5 - 7 years