Job Market Guide: Regulatory Affairs Specialist jobs in San Francisco-Oakland-San Jose

Competition
Low
0.183341
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Regulatory Affairs Specialists in San Francisco-Oakland-San Jose. Regulatory Affairs Specialists in San Francisco-Oakland-San Jose have between ${} and ${} years of experience, averaging $${} years of experience.

9 Regulatory Affairs Specialist jobs in San Francisco-Oakland-San Jose

$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

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

Sunnyvale, CA
Assess the impact of the product/process changes and determine regulatory pathway for US, EU and Canadian markets.
industry
Patient Care
experience
8 - 10 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

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
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

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

$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