Fda jobs in Irvine

BaRupOn LLC

A leading company in pharmaceuticals seeks a Regulatory Affairs Specialist to ensure compliance with FDA and DEA regulations. This role involves preparing submissions, maintaining licenses, and coordinating audits while working closely with regulatory agencies. Ideal candidates will have a backgroun

Medtronic

We anticipate the application window for this opening will close on - 15 Apr 2026 A Day in the Life Medtronic is seeking an FDA/Life Sciences lawyer as a member of the Enterprise Legal Regulatory (ELR) team with knowledge and experience navigating requirements for regulated industries. The ELR team

BaRupOn LLC

Job Summary The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audits, and staying ahead of evolv

BaRupOn LLC

Regulatory Affairs Specialist (FDA, DEA) The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audit

A leading staffing firm is seeking a Digital Lab Email Specialist to manage email marketing programs in a regulated FDA-compliant environment. Responsibilities include building and testing emails, coordinating with stakeholders, and ensuring compliance. Ideal candidates have 3-5 years of email marke

A medical device corporation is looking for a Senior Project Manager to oversee complex projects in Consumables R&D. This role requires extensive experience in project management, especially in FDA-regulated environments. The candidate will lead diverse teams, ensure compliance with quality standard

BaRupOn LLC

Job Summary The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audits, and staying ahead of evolv

BiVACOR

A leading medical device manufacturer in Huntington Beach is seeking an experienced Quality Inspector IV to support the development of a world-first Total Artificial Heart. This role involves hands-on inspection in an FDA-regulated environment, requiring strong knowledge of quality standards and tec

Innovative Career Resources & Staffing

A recognized medical diagnostics manufacturer in Southern California is seeking a Senior Quality Control Inspector to ensure regulatory compliance and product quality. The ideal candidate will have over 5 years of experience in FDA-regulated environments, a strong understanding of ISO 13485, and pro

National Institute of Clinical Research, Inc.

A leading clinical research organization in California is seeking an experienced Quality Assurance Specialist to ensure the accuracy and compliance of clinical research data. This role requires overseeing audits and compliance with FDA regulations while providing training to research staff. Candidat

A leading dental products company in Irvine, California, is seeking a Regulatory Affairs professional to manage product registrations and ensure compliance with FDA and other regulatory bodies. The ideal candidate will have over five years of experience and a Bachelor's degree in a related field. Th

A leading Biotech Consultancy firm is seeking a SAP Computer System Validation (CSV) Analyst to join their remote team. This role involves reviewing and validating SAP test scripts in a GxP-regulated environment. Ideal candidates should have over 3 years of SAP CSV experience, strong knowledge of FD

A leading medical device company seeks a Quality Engineer for Risk Management in Irvine, CA. This role involves developing compliant risk management frameworks for cardiac devices and ensuring adherence to FDA regulations. Candidates should have 8–12 years of experience in Medical Device Quality, fo

A leading firm in Medical Devices is seeking a Senior Quality Engineer in Irvine, California. The successful candidate will establish a compliant risk management framework and lead remediation efforts for existing documentation. Ideal applicants will have over 7 years of experience in Medical Device

A healthcare staffing company is seeking a Senior Quality Engineer to establish a compliant risk management framework for medical devices. This role involves leading risk management efforts, supporting design documentation compliance, and working collaboratively with cross-functional teams. Candidat

A leading dietary supplement manufacturer in California is looking for a Production Supervisor to oversee production activities. This position requires 3-5 years of supervisory experience in an FDA environment, alongside strong communication and multitasking skills. The supervisor will ensure that a

Dice is the leading career destination for tech experts at every stage of their careers. Our client, Optimus Labs USA, is seeking the following. Apply via Dice today! *EA-DE IT O-** *ECC & SAP S/4HANA Finance & Controlling (FICO) Architect with FDA, SOX, IFRS** *-** *Brea CA - Onsite work**

EA-DE IT O- ECC & SAP S/4HANA Finance & Controlling (FICO) Architect with FDA, SOX, IFRS - Brea CA - Onsite work Requisition Name : EA-DE IT O-SAP Financial Accounting Architect Start Date : 3/23/2026 Duration : 31 Weeks Services Location : CA/Brea Description Of Services : Role Overview We

BaRupOn LLC

Job Summary The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audits, and staying ahead of evolv

BaRupOn LLC

Job Summary The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audits, and staying ahead of evolv