Regulatory affairs jobs in Santa Ana, CACreate job alerts

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas –...

This is a critical role within a mission-driven, collaborative environment—and an exciting opportunity to be the first hire on a newly expanding Regulatory Affairs team. Regulatory Affairs Analyst – CPG Industry. A leading and rapidly growing CPG brand in the wellness space is seeking a Regulato

Job DescriptionDescription: Company Overview CMBG3 Law is majority women-owned nationwide law firm comprised of a diverse team of pro-active trial attorneys, litigators, consultants, paralegals, and staff. CMBG3 Law takes a proactive approach to solving legal problems through best-in-class busin...

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas –...

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas –...

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas –...

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas –...

Job DescriptionOverview Allied Universal®, North America's leading security and facility services company, offers rewarding careers that provide you a sense of purpose. While working in a dynamic, welcoming, and collaborative workplace, you will be part of a team that contributes to a culture tha...

Job DescriptionJob Description Crowell & Moring LLP is an international law firm with offices in the United States, Europe, MENA, and Asia that represents clients in litigation and arbitration, regulatory and policy, intellectual property, and transactional and corporate matters. The firm is in...

Job DescriptionSalary: $30$35 Hourly, DOE About AmeriPharma AmeriPharma is a rapidly growing healthcare company where you will have the opportunity to contribute to our joint success on a daily basis. We value new ideas, creativity, and productivity. We like people who are passionate about the...

Job DescriptionDescription: Company Overview CMBG3 Law is WOSB/WBENC certified majority women-owned nationwide law firm comprised of a diverse team of pro-active trial attorneys, litigators, lobbyists, consultants, paralegals, and staff. CMBG3 Law takes a proactive approach to solving legal prob...

Job DescriptionPURPOSE: The position of Regulatory Specialist II in Nutrition reports to the Sr. Manager and will work closely with R&D and Marketing. This position will entail ensuring the compliance of nutritional products in the countries that Arbonne does business in. These will include perf...

Job DescriptionAbout the Firm Talley, LLP, and its affiliated entities, Talley Law Group, LLP (“TLG”), Talley Capital Group, LLC (“TCG”) and Talley Client Accounting Services, LLC (“TCAS” fka Group 11) (collectively “Talley”) is a full service financial, tax, legal and consulting organization de...

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas –...

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas –...

Job Description At Geiss Med Hospice, we believe in cherishing every moment of life. We understand that facing a life-limiting illness or injury can be overwhelming, which is why we are here to provide a comforting hand and a listening ear. Our team of dedicated medical professionals and compassi...

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas –...

Job DescriptionDescription: AVITA Medical® is a therapeutic, acute wound care company leading the development and commercialization of devices and autologous cellular therapies for skin restoration. Our FDA-approved RECELL® System technology platform treats patients with thermal burn wounds and...

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas –...

Job Description P2|P2|C1|LCA.04.022.P20|General Product Regulatory Affairs - Experienced Professional (P2)|51|C1 Regulatory Specialist II – Personal Care Why You're Here The Regulatory Affairs Specialist II – Personal Care reports to the Sr. Manager, RSA and will work closely with Produ...

Job Description IN HOUSE GENERAL COUNSEL SCOPE OF WORK • Represents all legal and compliance matters of personal and all business entities currently in place or in the future.”, • Provides overall leadership and management of all corporate, employment and commercial legal matters, facilitatin...

Job DescriptionDescription: Company Overview CMBG3 Law is WOSB/WBENC certified majority women-owned nationwide law firm comprised of a diverse team of pro-active trial attorneys, litigators, lobbyists, consultants, paralegals, and staff. CMBG3 Law takes a proactive approach to solving legal prob...

BEPC is actively looking for a Controls Validation Engineer in Irvine, CA W2 Contract - 6 months with possible extensions! Benefits include medical, dental, vision, and life insurance Work Arrangement: 100% On-site Compensation: $50.00-$55.00/hour Open depending on experience Note: This ...

REGULATORY AFFAIRS PROJECT MANAGER About MicroPort®: As an innovative high-end medical device group, MicroPort® was founded in 1998 in ZJ Hi-Tech Park in Shanghai, China. It has 400+ products on the market and more than 6,800 patents (including patent applications) and 25 products entitled t...

Reviews and revises regulatory submissions to effectively present data and strategy to regulatory agencies. Preferred Experience: 10 years pharmaceutical experience including 5-plus years in regulatory affairs or 5-plus years in Discovery, R&D, or Manufacturing. The Senior Manager, Regulatory Aff...

The ideal candidate is a mid-level professional with a proven track record of managing projects through design verification (DV) and regulatory submissions, specifically with 510(k) and Pre-Market Approval (PMA) experience. Lead cross-functional teams, including R&D, Quality, Regulatory Affairs, ...

Responsibilities: Prioritize and monitor cases throughout the day, provide status updates as necessary.Support the IVDR labeling conversion and revisions of technical files for appropriate products that are due to convert to the new IVD Regulation.Work cross-functionally in weekly meetings to ens...

From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and international regulatory environments. Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, includin...

Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and resolving moderately sophisticated conflicts between those requirements and development issues; a...

From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and international regulatory environments. Represent the regulatory function on manufacturing and product development teams as a subject matter expert (SME) to provide input on ...

The Coordinator of Regulatory Affairs assists with ensuring compliance with all relevant healthcare regulations and standards including the Joint Commission (TJC), the California Department of Public Health (CDPH), the Centers for Medicare and Medicaid Services (CMS), and other regulatory agencie...

Associate II, Regulatory Affairs Strategy supporting the Global Regulatory Team in Lake Forest, Irvine, CA, Fort Worth, Houston, TX, or Sinking Springs, PA, a typical day will include:. Associate II, Regulatory Affairs Strategy. Perform specialized tasks and conduct independent research within th...

The Regulatory Affairs Manager, under the general direction of the Assistant Director, will serve as a senior-level expert in clinical research protocols and regulatory processes within the Alpha Clinic. The Regulatory Affairs Manager applies extensive knowledge of clinical research protocols and...

MicroPort Scientific America is seeking a highly experienced and credentialed Project Manager, Vertical Marketing and Regulatory Affairs, to lead and execute regulatory and go-to-market strategy on high profile projects across our medical device portfolio. Bachelor’s degree in life sciences, engi...

Regulatory Affairs Specialist - Food Manufacturing** Manufacturing San Fernando Valley , CA, US Pay Rate Low: 30 | Pay Rate High: 35 + Added - 30/07/2025 Apply for Job Position Overview We're seeking an experienced Regulatory Affairs Specialist to join our growing tea

The Regulatory Affairs Manager will be appointed to participate as an active member of Industry regulatory or scientific committees and will have the opportunity to network with Industry peers. Associate Specialist – Premarket Regulatory Affairs. Regulatory Affairs Specialist - SaMD/SiMD.

This role will be responsible for Regulatory Affairs support of submissions and ongoing regulatory compliance for product development process, as well as developing regulatory strategies. EU regulatory filings for new and modified Class III products Provides technical reviews of test protocols an...

Regulatory Affairs Specialist - Food Manufacturing** Manufacturing San Fernando Valley , CA, US Pay Rate Low: 30 | Pay Rate High: 35 + Added - 30/07/2025 Apply for Job Position Overview We're seeking an experienced Regulatory Affairs Specialist to join our growing team and lead regulatory com...

The Regulatory Affairs Manager will be appointed to participate as an active member of Industry regulatory or scientific committees and will have the opportunity to network with Industry peers. Regulatory Affairs and Compliance Analyst (Medicare). Regulatory Affairs Specialist III - Urology.

Prismatik Regulatory Affairs Position. Minimum five (5) years of experience in Regulatory Affairs. Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.

Responsibilities: Regulatory Labelling Documentation. Support the creation and maintenance of assigned labeling projects to enable worldwide regulatory submissions. Independently prepare and maintain the Tracking Sheets for the global regulatory dossiers related to labeling projects in close coll...

The Senior Regulatory Affairs Specialist is responsible for Regulatory Affairs support of submissions and ongoing regulatory compliance for product development process and sustaining engineering projects, ensuring compliance with FDA regulations, ISO standards, and other regulatory agencies. Prov...

Regulatory Affairs is responsible for planning, coordinating and implementing regulatory strategies for products that require government approval.

Preferred Experience: 5 years in regulatory affairs. The Associate Director, Regulatory Affairs Devices And Combination Products works with internal and external partners to deliver products to patients. Support the development of the device regulatory strategy and provide device input into the p...

Responsibilities: The Regulatory Affairs Manager is responsible and accountable for Company Core Data Sheets (CCDS), Company Core Safety Information (CCSI) and Reference Safety Information (RSI) for assigned products, including regulatory responsibilities in associated change control and labeling...