Average salary: $112,000 /yearly
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...Job Title: Regulatory Affairs Specialist
Job Responsibilities:
This position is responsible for providing guidance on regulatory requirements as well as assisting in regulatory related projects and tasks ensuring compliance with FDA regulations, ISO...
Regulatory
...environment, the core of our success is its people with the commitment to a better healthcare experience. When you join us as a Clinical Regulatory Specialist you will be joining a dedicated team of professionals who deliver quality, value, and access in the 21st century and...
Regulatory
Job TitlePrincipal Regulatory Affairs SpecialistJob DescriptionPrincipal Regulatory Affairs Specialist (U.S. Hub based)Clinical Integration and Insight (CII) is changing the way healthcare is delivered at the point of care. Our Capsule Surveillance product is a clinical...
Regulatory
Local area
Remote job
Worldwide
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Overview:
Represents the Regulatory Affairs function in project teams, and manages regulatory projects to established timelines and budgets. Oversees and ensures compliance with state, federal and International medical device regulations and overall regulatory departmental...
Regulatory
...The Regulatory Affairs Specialist temp is responsible for developing and influencing regulatory policy and determining and pursuing courses of action necessary to obtain regulatory approval for the organizations products. Work with RA Leadership and other members of the...
Regulatory
Holiday work
Contract work
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Afternoon shift
...at Prismatik
Essential Functions :
Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.
Maintains company registrations and device listings in the US, Canada, and the EU.
Analyzes and reports department...
Regulatory
Holiday work
...Position Overview: Join Applied Medical and play a crucial role in revolutionizing medical devices. As a Specialist in Premarket Regulatory Affairs, you will play a pivotal role in ensuring compliance with regulatory requirements during the early stages of product...
Regulatory
Holiday work
Local area
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Overview:
The Director, Regulatory Affairs for EMEA is responsible for successful completion of complex regulatory projects, including pre-submissions and IDE submissions to FDA, IRB submissions, Ethics Committee submissions, EU Annex XIV submissions and as well as...
Regulatory
Remote job
Local area
...personal touch. For more information, visit Follow Allergan Aesthetics on LinkedIn.
Job Description
Description
The Manager Regulatory Affairs represents US regulatory affairs for device development projects. Executes US regulatory strategic plans and provides...
Regulatory
Holiday work
Temporary work
Local area
...creating next-generation solutions that address unmet medical needs.
The primary responsibility of the position is to support regulatory strategy and registration across global markets for a defined group of MedAlliance/Cordis products, drive regulatory processes...
Regulatory
Worldwide
Work visa
...Reports, Design Dossier, Technical Files, Australian Technical Files, Canadian Licenses, and Japan submissions. Essential Requirements Checklists, Design Dossiers, Technical Files and De Regulatory, Remote, Neuro, Principal, Specialist, Technical, Manufacturing, Education...
Regulatory
Remote job
...AbbVie, please visit us at Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.
Job Description
The Manager, Regulatory Affairs In Vitro Diagnostics and Companion Diagnostics works with internal and external partners to develop and implement global...
Regulatory
Remote job
...Virgin Galactic Regulatory Specialist Tustin , California Apply Now
As a Project Specialist supporting the Regulatory team at Virgin Galactic you will support critical activities towards establishing and ensuring compliance with regulatory requirements related to our...
Regulatory
Permanent employment
Full time
...Description
We're looking for a Regulatory Affairs Associate , working in Biotechnology/Medical Devices industry in 100 Abbott Park Road, Lake Forest, Illinois, 60064, United States .
Job description:
Responsible for filing necessary applications and...
Regulatory
...global regulations relevant to medical devices, Class II and/or Class III devices
Solid knowledge and understanding of global regulatory requirements for new products or product changes.
Solid knowledge of new product development systems
Strict attention to detail...
Regulatory
...$81,390.40 - $115,835.20 Annually
Location : Irvine, CA
Job Type: Full-Time Regular
Job Number: 00792
Department: Regulatory Compliance
Opening Date: 05/01/2024
Closing Date: 5/26/2024 11:59 PM Pacific
General Description
Irvine Ranch...
Regulatory
Holiday work
Full time
Internship
About Finfare
Finfare is dedicated to empowering SMBs, by providing the ultimate expense management solution for growing businesses seeking to streamline their financial operations and maximize cash back rewards. Finfare offers easy expense tracking, personalized spend...
Regulatory
Fixed term contract
Local area
...independently or as part of a team.
This is a full-time position based in Santa Ana/Costa Mesa, California.
The role of a Regulatory Affairs Manager is crucial in ensuring that our products comply with regulations and laws governing their manufacturing, sale,...
Regulatory
Full time
Flexible hours
Day shift
Monday to Friday
...neurovascular devices in the world. We deliver excellence through innovation with integrity.
Reporting directly to the CEO, the Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning...
Regulatory
...hours, and premium lifestyle amenities at our corporate campus in Irvine, California.
Status
Exempt
Summary
The Senior Regulatory Compliance Manager is principally responsible for definition and management of Kia's CAF and GHG compliance strategies, and...
Regulatory
Holiday work
Work experience placement
