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.

19 Regulatory Affairs Specialist jobs in CA

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

Los Angeles, CA
In this role, the selected candidate will execute actions necessary for license supplements to ensure that Grifols is in compliance with domestic and international licensing requirements and business objectives are met.
industry
Manufacturing / Diversified
experience
Less than 5 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

San Diego, CA
In this role, the selected candidate will be responsible to design control documentation to ensure compliance with domestic and international regulatory requirements for ivd medical devices.
industry
Business Services
experience
Less than 5 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

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

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

Mountain View, CA
In this role, the selected candidate will evaluate complaints to determine whether an investigation is necessary and if Medical Device Reporting (MDR) is necessary in accordance with 21 CFR Part 803 Medical Device Reporting and 806 Corrections and Removals.
industry
Medical Devices & Diagnostics
experience
Less than 5 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

Irvine, CA
In this role, you will develop US and International regulatory strategies for product submissions, identifying needs for bench, animal and clinical testing.
industry
Medical Devices & Diagnostics
experience
Less than 5 years

Fremont, CA
In this role, the selected candidate will prepare regulatory submissions (BLA and IND) and related maintenance documentation (amendments, supplements, annual reports, Drug and Site Master File maintenance, etc.) for US and other Regulatory Health Authorities within defined time schedule.
industry
Business Services
experience
5 - 7 years

Irvine, CA
In this role, you will be responsible to support the implementation of various process improvement projects working directly with key stakeholders in all business units as well as our international counterparts to accelerate route to market access.
industry
Healthcare IT
experience
Less than 5 years

Corona, CA
In this role, you will be responsible for formulation and labeling tweaks to ensure that our product lines are in compliance with regulations in international markets.
industry
Business Services
experience
5 - 7 years

San Diego, CA
In this role, you will determine/document appropriate regulatory strategy for proposed new products and initiate necessary activities by working with Regulatory management as needed.
industry
Medical Devices & Diagnostics
experience
Not Specified

Fremont, CA
In this role, the selected candidate will advise internal stakeholders (marketing, manufacturing, R&D, etc.) regarding current/pending guidance, regulations, Agency/industry initiatives, etc. to ensure regulatory strategy is in alignment with company objectives.
industry
Biotech/Pharma
experience
5 - 7 years

Carlsbad, CA
In this role, you will be responsible for review and prepare regulatory documents for submission to FDA in compliance with requirements. Documents may include Agency Meeting Requests, Briefing Documents, CMC and Labeling supplements, General Correspondence, Annual Reports and Periodic Safety Reports.
industry
Life Sciences & Research
experience
8 - 10 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

Irvine, CA
In this role, you will participate on Product Development teams, providing regulatory strategy, timelines, and direction.
industry
Medical Devices & Diagnostics
experience
Less than 5 years

$125K - $145K - Menlo Park, CA
In this role, the selected candidate will oversee and manage assembly and publishing of all documents while maintaining adherence to FDA standards and internal requirements.
industry
Business Services
experience
Less than 5 years