Job Market Guide: Regulatory Affairs Specialist jobs in San Diego

Competition
Low
0.036453
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Regulatory Affairs Specialists in San Diego. Regulatory Affairs Specialists in San Diego have between ${} and ${} years of experience, averaging $${} years of experience.

9 Regulatory Affairs Specialist jobs in San Diego

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
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
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

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

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

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

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

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