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Corporate Jobs in Riverdale, GA

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Supervisor, Regulatory Affairs Inland Empire Health Plan

Rancho Cucamonga, California

$104,041.60–$137,841.60 / year
Full time

In partnership with the Regulatory Affairs Manager, the Supervisor plays a critical role in maintaining organizational compliance with complex requirements issued by the Centers for Medicare and Medicaid Services (CMS), Department Health Care Services (DHCS), Department of Managed Health Care (DMHC), and Covered California, as these apply to the team’s assigned line of business. Deep understanding of Federal and State regulatory frameworks governing Medi-Cal (Medicaid), Medicare, and related statutory and regulatory authorities, including Title 19 (USC) / Title 29 (USC and CFR), Title 22 (CCR), Title 28 (CCR), Title 42 (USC and CFR), California Welfare and Institutions Code (WIC), and the California Health and Safety Code.

30+ days ago

Manager, Policy and Regulatory Affairs Weave Grid Inc.

San Francisco, CA

$110,000–$156,000 / year

Utilizing modern, cloud-native platform architecture and robust systems optimization, WeaveGrid's software is built from the ground up to tackle the most critical network challenges while meeting the stringent regulatory, security, and reliability requirements of the utility industry. This role will be focused on policy and regulatory strategy in one or more subsets/regions of the United States while working hand-in-hand with the business's leaders to inform WeaveGrid's strategy and sales priorities.

30 days ago

Senior Manager / Associate Director, Regulatory Affairs CMC (Small Molecules) Nurix Therapeutics, Inc.

Brisbane, CA

$187,800–$208,600 / year

Author, review, and compile high-quality CMC (Module 3 / Quality) content for regulatory submissions, including IND/IMPD and equivalent global filings, amendments, annual reports, and responses to health authority questions. You'll combine hands-on authoring of Module 3 (Quality) content with real strategic influence as the CMC regulatory voice on cross-functional teams, with room at the Associate Director level to own strategy and mentor junior regulatory staff.

14 days ago

Manager, Regulatory Affairs Arrowhead Pharmaceuticals Inc

San Diego, CA

$145,000–$160,000 / year

Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes.

30+ days ago

Senior Manager / Associate Director, Regulatory Affairs CMC Small Molecules Nurix Therapeutics Inc

Brisbane, CA

$187,800–$208,600 / year

Author, review, and compile high-quality CMC (Module 3 / Quality) content for regulatory submissions, including IND/IMPD and equivalent global filings, amendments, annual reports, and responses to health authority questions. You''ll combine hands-on authoring of Module 3 (Quality) content with real strategic influence as the CMC regulatory voice on cross-functional teams, with room at the Associate Director level to own strategy and mentor junior regulatory staff.

14 days ago

Senior Manager/Associate Director, Regulatory Affairs (Strategy, Hematology Oncology) Nurix Therapeutics, Inc.

Brisbane, CA

$187,800–$208,638 / year

Works strategically with all regulatory functions to develop detailed, actionable submission plans, tracks major submission deliverables, and ensures consistent management submission documents, health authority communications, and all other regulatory information supporting Nurix's investigational and marketing applications. Job Summary: In this role, you will be a core member of the Regulatory team and will be responsible for helping build and execute on global regulatory strategy, objectives, policies and programs pertaining to development and future marketing of products.

30+ days ago

Regulatory Affairs Manager - Diabetes Care (on-site) Abbott Laboratories

Milpitas, CA

$114,000–$228,000 / year

As a member of the U.S. Regulatory Affairs management team, the successful candidate will lead and develop talent, shape regulatory strategy, and partner across functions to bring innovative products to market, whilst driving regulatory excellence for the manufacture, change management, and ongoing supply of the Libre portfolio. Drive and provide strategic guidance on FDA pathways, submissions, and interactions, including pre-submissions, 510(k), PMA, and post-market activities.

30+ days ago

Senior Manager/Associate Director, Regulatory Affairs Strategy, Hematology Oncology Nurix Therapeutics Inc

Brisbane, CA

$187,800–$208,638 / year

30+ days ago

Senior Manager, Regulatory Affairs and Compliance Traditional Medicinals Inc

Rohnert Park, CA

$155,900–$204,645 / year

The role serves as the functional leader for Regulatory Affairs and Compliance at the Company, with responsibility for establishing regulatory strategy, providing authoritative regulatory guidance, and building and operating the systems, governance, and capabilities necessary to support the Company's growth. The ideal candidate is equally comfortable interpreting regulatory requirements, coordinating cross-functional compliance activities, supporting audit/inspection readiness, and building scalable processes that reduce reliance on fragmented/manual coordination.

30+ days ago

Regulatory Affairs Coordinator University of California, Irvine

Orange, California

Full time

Proven organizational skills and attention to detail; ability to multi-task, prioritize a complex and dynamic workload, meet rigid deadlines despite interruptions, frequent workload changes and competing demands, and achieve high productivity/quality within short time frames; skill in working independently, taking initiative and following through on assignments and ability to work as part of a team. *Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.

30+ days ago

Sr. Specialist, Regulatory Affairs Metagenics LLC

Aliso Viejo, CA

Industry Surveillance: Monitors competitive claims, FDA's and FTC''s actions, litigation, news releases and other sources, as they relate to the current science of Metagenics-related products and challenges to relevant product claims, to ensure that Metagenics limits its exposure for product claims both domestically and internationally. The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs.

30+ days ago

Manager, Regulatory Affairs Noctrix Health

Pleasanton, California

$150,000–$180,000 / year

The Manager, Regulatory Affairs will work closely with Clinical Affairs, Quality, Engineering, Operations, Marketing, and external regulatory partners to provide regulatory guidance, manage submissions, assess product changes, maintain global registrations, and support post-market regulatory activities. We are seeking an experienced and highly organized Manager, Regulatory Affairs to lead and execute regulatory activities supporting the development, registration, commercialization, and post-market compliance of Noctrix Health’s medical devices.

30+ days ago

Senior Regulatory Affairs Specialist Route 92 Medical Inc

San Mateo, CA

Demonstrated ability to independently manage regulatory submissions, registrations, amendments, and renewals across multiple countries and regulatory frameworks simultaneously - including identifying country-specific requirements, preparing documentation, managing timelines, responding to regulatory questions, and maintaining existing market authorizations. This role will independently prepare and maintain international regulatory submissions and registrations, conduct regulatory assessments of product and Quality System changes, and work with regulatory authorities, in-country representatives, distributors, and other regulatory partners to obtain and maintain market authorization.

23 days ago

Regulatory Affairs Specialist II Envista Holdings Corp

Brea, CA

$85,800–$104,800 / year

This individual is responsible for obtaining global regulatory registrations/approvals based on company objectives, attending product development meetings, regional alignment; as well as collaborating with cross-functional departments to ensure country-specific requirements are met and integrated throughout the design control and post-product launch activities. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening.

30+ days ago

Regulatory Affairs Specialist Envista

Brea, CA

$85,800–$104,800 / year

30+ days ago

Director, Regulatory Affairs - Advertising, Promotional And Labeling #4810 Grail

Sunnyvale, CA

$189,000–$271,000 / year

The Director serves as a senior regulatory subject-matter expert and strategic business partner, who leads cross-functional teams in developing promotional materials to ensure compliance with global regulatory markets, while capturing potential regulatory risks. We have built a multi-disciplinary organization of scientists, engineers, and physicians and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicine's greatest challenges.

30+ days ago

Senior Regulatory Affairs Labeling Specialist Procept Biorobotics Corp

San Jose, CA

$121,890–$143,400 / year

Represent the Regulatory Affairs labeling function on project teams by collecting potential labeling inputs from other departments; interpreting the impact that projects, such as design changes, will have on labeling content; and implementing necessary modifications to the product labeling. It continues with our one-of-a-kind management program designed to build the best managers in the industry, where our people managers across functions come together to exchange ideas and grow, as both managers and learners, in an environment that challenges, supports and broadens.

30 days ago

Senior Regulatory Affairs Labeling Specialist Procept Biorobotics

San Jose, CA

$121,890–$143,400 / year

30 days ago

Sr. Regulatory Affairs Specialist, Medical Devices (Long Beach, CA) Beauty Health

Long Beach, CA

This includes developing regulatory planning, preparing submissions, ensuring ongoing compliance with applicable regulations such as U.S. FDA and international market regulations, and supporting cross-functional teams to bring innovative solutions to market safely and efficiently. An employee's pay position within the salary range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, seniority, geographic location, performance, travel requirements, revenue-based metrics, any contractual agreements, and business or organizational needs.

15 days ago

Sr. Regulatory Affairs Specialist, Medical Devices BeautyHealth

Long Beach, California

$107,500–$125,000 / year

This includes developingregulatory planning, preparing submissions, ensuring ongoing compliance with applicable regulations such as U.S. FDA and international market regulations, and supporting cross-functional teams to bring innovative solutions to market safely and efficiently. An employee’s pay position within the salary range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, seniority, geographic location, performance, travel requirements, revenue-based metrics, any contractual agreements, and business or organizational needs.

4 days ago

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Corporate Jobs in Riverdale, GA

Supervisor, Regulatory Affairs Inland Empire Health Plan

Manager, Policy and Regulatory Affairs Weave Grid Inc.

Senior Manager / Associate Director, Regulatory Affairs CMC (Small Molecules) Nurix Therapeutics, Inc.

Manager, Regulatory Affairs Arrowhead Pharmaceuticals Inc

Senior Manager / Associate Director, Regulatory Affairs CMC Small Molecules Nurix Therapeutics Inc

Senior Manager/Associate Director, Regulatory Affairs (Strategy, Hematology Oncology) Nurix Therapeutics, Inc.

Regulatory Affairs Manager - Diabetes Care (on-site) Abbott Laboratories

Senior Manager/Associate Director, Regulatory Affairs Strategy, Hematology Oncology Nurix Therapeutics Inc

Senior Manager, Regulatory Affairs and Compliance Traditional Medicinals Inc

Regulatory Affairs Coordinator University of California, Irvine

Sr. Specialist, Regulatory Affairs Metagenics LLC

Manager, Regulatory Affairs Noctrix Health

Senior Regulatory Affairs Specialist Route 92 Medical Inc

Regulatory Affairs Specialist II Envista Holdings Corp

Regulatory Affairs Specialist Envista

Director, Regulatory Affairs - Advertising, Promotional And Labeling #4810 Grail

Senior Regulatory Affairs Labeling Specialist Procept Biorobotics Corp

Senior Regulatory Affairs Labeling Specialist Procept Biorobotics

Sr. Regulatory Affairs Specialist, Medical Devices (Long Beach, CA) Beauty Health

Sr. Regulatory Affairs Specialist, Medical Devices BeautyHealth

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