A company is looking for a Principal Regulatory Affairs Specialist, US Regulatory Policy. FDA regulatory requirements and policyRegulatory experience within the medical device industry or a regulatory agencyExperience in advocacy related to healthcare policy and regulationsStrong research and analyt...
Title** : Regulatory Affairs Specialist (Senior Level). We are seeking a Regulatory Affairs Specialist (Senior Level) to ensure company compliance with US FDA 510(k), Health Canada Licensing, International Device Submissions, Licensing and Registration requirements, ISO/FDA QSR, and ISO 13485. Manag...
A company is looking for a Regulatory Affairs Specialist responsible for managing regulatory activities related to the Lung Health product portfolio. ...
Title** : Regulatory Affairs Specialist with a Specialty in Labeling. Regulatory Affairs Certification is preferred but not required. Partners with other functions and Subject Matter Experts (SME's) to obtain information and/or data required for regulatory submissions. Anticipates regulatory obstacl...
A company is looking for a Senior Regulatory Affairs Specialist, Medical Devices. ...
In this role, you will Perform regulatory assessments for product changes including regulatory reportability decisions Work with cross functional team and international regulatory colleagues to develop and implement global regulatory strategy to support business global expansions Support regulatory ...
The Sr Regulatory Affairs Specialist is responsible for ensuring digital medical device regulatory clearance to enable market access by demonstrating compliance to applicable regulations through a registration dossier. Position: Sr Regulatory Affairs SpecialistLocation: Sunnyvale, CaliforniaPosition...
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, including p...
We are currently seeking a Senior Regulatory Affairs Specialist to drive regulatory strategies and submissions for medical devices. Senior Regulatory Affairs Specialist. Hands-on experience with major regulatory submissions and managing interactions with regulatory agencies. Develop and implement gl...
Medical manufacturer is hiring a Regulatory Affairs Specialist on a temporary basis. Previous medical device experience in a Regulatory Affairs capacity . ...
Job Description: Regulatory Affairs Specialist. Provide consultation and advice to regulatory specialists regarding change control and product development. Contribute to continuous improvement initiatives within the regulatory affairs function. Ability to interpret and apply regulatory requirements....
Regulatory Affairs Specialist (Senior Level). We are seeking a Regulatory Affairs Specialist (Senior Level) to ensure company compliance with US FDA 510(k), Health Canada Licensing, International Device Submissions, Licensing and Registration requirements, ISO/FDA QSR, and ISO 13485. Managing and Dr...
Regulatory Affairs Specialist II. Regulatory Affairs Specialist II:. Regulatory Affairs Specialist II:. Works in close collaboration with internal customers and supports multiple projects to align on regulatory strategy to achieve business objectives. ...
Regulatory Affairs Specialist with a Specialty in Labeling. Regulatory Affairs Certification is preferred but not required. Partners with other functions and Subject Matter Experts (SME's) to obtain information and/or data required for regulatory submissions. Anticipates regulatory obstacles and eme...
Program Manager, Housing Navigation. The Housing Navigation Program Manager will provide oversite to case management staff that are responsible for field-based services to single adults experiencing homelessness as they transition into permanent housing. The Program Manager is also responsible for b...
The Manager CMC Regulatory Affairs is responsible for CMC technical document review and writing, authoring and compiling the CMC sections for global regulatory filings by working closely with the cross-functional teams including CMC, Quality, Clinical and Regulatory Affairs to ensure all Regulatory ...
The AD CMC Regulatory Affairs supports the development and successful performance of the CMC regulatory strategy for the innovative pipeline of early-stage T cell therapies. This position is hybrid, and based in Santa Monica, CA and reports to the Executive Director, CMC Regulatory Affairs. Represen...
The Manager CMC Regulatory Affairs is responsible for supporting the development and successful performance of the CMC regulatory strategy for the innovative pipeline of early and late-stage T cell therapies. Director, CMC Regulatory Affairs. Represent CMC regulatory affairs on product teams and in ...
A company is looking for a Manager, Materials (Program Development). ...
A company is looking for an Associate Program Manager to provide technical leadership in analytics projects. ...
A company is looking for a Payroll Compliance Analyst for a national remote position. ...
A company is looking for a Senior Regulatory Compliance Specialist. ...
A company is looking for a Regulatory Manager to join their Corporate Counsel team. ...
A company is looking for a Senior Associate in US Regulatory Affairs. ...
A company is looking for an Engineering Program Manager. Key Responsibilities:Enhance Engineering Onboarding experience and curate essential resourcesLead Engineering enablement efforts by organizing training sessions and curating resourcesManage Engineering blog, team engagement, and meeting agenda...