Regulatory Affairs Manager jobs
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SENIOR REGULATORY AFFAIRS PROGRAM LEAD
...
| Company | Johnson & Johnson |
|---|---|
| Address | Raynham, MA |
| Category | Information Technology |
| Date Posted | a month ago See detail |
Director, Regulatory Affairs
Biospace
San Diego, CA
Accountable for the development and implementation of the regulatory strategy for AnaptysBios pipeline programs. Serve as the FDA contact, leading creative and constructive interactions with regulatory agencies to effectively neg...
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- View all Biospace jobs - jobs in San Diego, CA
AML Monitoring and Regulatory Manager - (M/F)
Axa
Delaware, United States
Assisting AXA entities in developing and enhancing their AML and targeted sanctions compliance programs, including policies, procedures, training programs, and monitoring processes. Providing accurate, timely, and consistent AML t...
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- View all Axa jobs - jobs in Delaware State
Regulatory Manager
Buckman Laboratories International, Inc.
Memphis, TN
Memphis, TN English Less than 10% Manages the flow of Regulatory Information and Consultation (ie: State Substances Lists, Prop 65, HAPS content, VOC Content, Local, State, and Federal Laws and Regulations, Ozone Depleting Subst...
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Public Affairs Manager, Security Engineering
Meta
New York, NY
$174,000 - $242,000 a year
Build and execute proactive communications programs for press, policy makers, and other groups that highlight the work Meta does to protect our community and company. Manage in-bound press inquiries on a range of time-sensitive is...
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Public Affairs Manager, Security Engineering
Meta
Menlo Park, CA
$174,000 - $242,000 a year
Build and execute proactive communications programs for press, policy makers, and other groups that highlight the work Meta does to protect our community and company. Manage in-bound press inquiries on a range of time-sensitive is...
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- View all Meta jobs - jobs in Menlo Park, CA
Regulatory Affairs Analyst
Brycetech
Washington, DC
CBRN Research and Analysis. CBRN Policy and Doctrine Support. Special Projects. Policy support to the Federal Radiological Preparedness Coordinating Committee (FRPCC). Planning support to the Chemical, Biological, Radiological/Nuc...
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SVP, Global Regulatory Affairs
Biospace
Waltham, MA
Ensure the development, preparation, and implementation of global strategic regulatory plan for all programs and product pipeline designed to maximize successful and expedient global product registrations. Responsible for managing...
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Associate Director, Regulatory Affairs
Biospace
San Rafael, CA
Lead the development, integration, execution and maintenance of the global nonclinical and clinical regulatory strategy for the Global Regulatory Plan (GRP) throughout the product lifecycle. Ensure strategic alignment with the Cli...
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- View all Biospace jobs - jobs in San Rafael, CA
Licensing & Regulatory Affairs Analyst
Sportradar
Las Vegas, NV
Tracking sports betting and iGaming legislative and regulatory efforts of new and existing jurisdictions with special focus on licensing requirements. Research, populate, and maintain internal library of country specific regulator...
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Principal Regulatory Affairs Specialist (medlance.co)
Medlance
Remote
$30 - $300 an hour
Lead regulatory strategy development for medical device projects. Manage submissions to regulatory bodies. Advise on regulatory requirements and changes. Collaborate with cross-functional teams for regulatory compliance. Extensive...
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Regulatory Affairs Specialist
Redbock- An Nes Fircroft Company
Remote
$70.9K - $89.8K a year
Prepare and maintain international submission dossiers. Prepare electronic pre-market and post-market regulatory submissions. Compile Technical Documentations for IVD medical devices. Monitor progress on project deliverables and p...
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Regulatory Affairs Senior Consultant
Medenvoy Global Bv
Remote
From $100,000 a year
Reviewing and processing of serious incidents related of medical devices of customers. Supervision of field safety corrective actions performed by clients. Communication with competent authorities and clients. Addressing post mark...
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Regulatory Affairs Specialist
Brs
Remote
$62.1K - $78.7K a year
Contractor shall have at least 5 years experience applying FDA research regulatory requirements within a research Regulatory Affairs program office. Work in preparing ones own research proposals and ones own submissions to an IR...
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Sr. Regulatory Affairs Specialist
Oxenham Group Llc
Saint Paul, MN
Writing and updating technical files to meet applicable regulatory requirements, to included Essential Requirements, General Safety and Performance Requirements, Device classification, compiling technical documentation, identifica...
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Principal Regulatory Affairs Specialist
Vertos Medical, Inc
Aliso Viejo, CA
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Mental Demand Moderate to high degree of concentration due to volume, complexity, and/or pressure of work. Abil...
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Staff/Principal Regulatory Affairs Specialist (Operations)
Recor Medical
Palo Alto, CA
Manages post market activities, including but not limited to EU MDR and MEDDEV compliant Clinical Evaluation documents for new products and maintain/update existing company Clinical Evaluation Plans (CEPs), Clinical Evaluation Rep...
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Senior Regulatory Affairs Specialist
Iconma, Llc
Saint Paul, MN
This position will be working with multiple business units to develop, update, and improve regulatory affair processes. Assist the strategy implementation and operations for Regulatory Affairs activities, including directing devel...
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Senior Regulatory Affairs Specialist
Axelon
Saint Paul, MN
This position will be working with multiple business units to develop, update, and improve regulatory affair processes. Assist the strategy implementation and operations for Regulatory Affairs activities, including directing devel...
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Senior Regulatory Affairs Specialist
Collabera
Saint Paul, MN
Perform assigned regulatory activities including submissions/responses to country authorities. Daily Responsibilities - suppliers should use: Plan and prepare documents for EU MDR Technical File original submiss...
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Director, Regulatory Affairs Specialty, HIV
Gsk
Olin, NC
Ensuring the regulatory strategy that will deliver the needs of the local region(s), taking in to account the needs of other regions globally. Implementation of the regional strategy(ies) in support of the project globally. Lead r...
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Director, CMC Regulatory Affairs Biologics
Biospace
California, United States
Lead CMC regulatory strategy for a single or multiple products. Lead the execution and influence the development of global CMC regulatory strategies, including risk mitigation strategies to ensure right first-time approvals of pro...
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- View all Biospace jobs - jobs in California State
Executive Director, Advertising & Promotions Regulatory Affairs
Ortho Dermatologics
Charleston, WV
$280,000 - $320,000 a year
Manages the Regulatory Promotional reviews for prescription drugs who represent Regulatory Affairs on the promotional review committee for marketed products. This position may require reviewing promotional materials if the company...
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- View all Ortho Dermatologics jobs - jobs in Charleston, WV
Public Affairs Manager
Citizens
Westwood, MA
$84.3K - $107K a year
Improve the reputation of the bank by bolstering brand visibility through cause-related marketing, colleague engagement and creating positive connections to the community. Execute local charitable contributions activities aligning...
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Director, Global Regulatory Affairs (GRL)
Biospace
Basking Ridge, NJ
Manages, directs, and drives the strategy for all Regulatory activities associated with the registration and support of new and approved drug products. Seeks and incorporate regional and functional RA strategy into a global strate...
2 months ago seen See more...
- View all Biospace jobs - jobs in Basking Ridge, NJ
Director, Regulatory Affairs Companion Diagnostics
Biospace
Basking Ridge, NJ
CDx development: Provide critical strategic and tactical regulatory guidance for CDx/IVD development and CDx submission plan for each country/region, both before and after CDx testing. At the time of implementation of a CDx study/...
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Associate Director, Regulatory Affairs - West Chester, PA
Teva Pharmaceuticals
United States
Spearhead the delivery of successful investigational and regulatory license applications and product life cycle management submissions with the Global Regulatory Affairs Team from initial filing through post-approval management. P...
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Senior Director, Regulatory Affairs CMC , Innovative Medicine (Hybrid)
Teva Pharmaceuticals
West Chester, PA
Influence the strategy and assess the quality of documents for regulatory submissions to major market health authorities as well as coordinate with global regulatory colleagues to prepare dossiers for global registration.. Ident...
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Executive Director, Regulatory Affairs
Biospace
San Diego, CA
Set strategy, direct, plan and implement clinical regulatory activities required to initiate and conduct clinical trials and to seek marketing authorization. Interact with the FDA, EMA, PMDA, and other regulatory agencies to seek...
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