FDA 510(k) Consultant Needed for Medical Device Submission

Opportunité d'été passionnante : Rejoignez notre équipe de dispositifs médicaux · Vous êtes un(e) étudiant(e) débordant d'enthousiasme, qui poursuit actuellement des études en ingénierie? Si c'est le cas, Jubilant Radiopharma vous invite à embarquer pour un voyage exaltant avec ...

Opportunité d'été passionnante : Rejoignez notre équipe de dispositifs médicaux · Vous êtes un(e) étudiant(e) débordant d'enthousiasme, qui poursuit actuellement des études en ingénierie? Si c'est le cas, Jubilant Radiopharma vous invite à embarquer pour un voyage exaltant avec ...

Opportunité d'été passionnante : Rejoignez notre équipe de dispositifs médicaux · Vous êtes un(e) étudiant(e) débordant d'enthousiasme, qui poursuit actuellement des études en ingénierie? Si c'est le cas, Jubilant Radiopharma vous invite à embarquer pour un voyage exaltant avec ...

+This Regulatory Affairs Specialist position works out of our Ottawa location in the Point of Care division. · +Bachelor's degree · Five plus years of relevant work experience · ...

We are seeking an experienced Consulting Biostatistician to lead the statistical strategy for an upcoming pivotal medical device clinical trial. · MS or PhD in Biostatistics, Statistics, or a closely related field. · Prior experience with FDA medical device submissions is require ...

I have an iOS app that needs to be fully prepared for deployment to the Apple App Store. · We are looking for an experienced iOS developer to help with the preparation of the app for deployment to the Apple App Store. The tasks include preparing the app for submission, uploading ...

We are seeking a detail-oriented professional to assist our company in preparing our mouthguard product for FDA registration.The ideal candidate will have experience in the regulatory submission process and a solid understanding of FDA requirements for medical devices. · ...

We are seeking a senior FDA regulatory consultant to support us up to and including IDE approval (Early Feasibility Study) · A critical objective of this engagement is to obtain early FDA alignment that the device represents a moderate-risk, Class II device suitable for the De No ...

We are seeking an experienced consultant to assist us in navigating the FDA approval process for our AI Murmur Analysis Software, · Scientific & Technical ServicesFDA510KMedical DeviceRegulatory Compliance ...

This position works under the direction of the Manager Regulatory Affairs to prepare regulatory documentation for i-STAT branded products. The individual has department level influence and performs specialized level work assignments and/or analyses, evaluation, preparation, and s ...

We are looking for an experienced app developer to assist with the submission of our app to the App Store. · iOS Development · Mobile App Development · ...

I am looking for an experienced WordPress and Elementor developer to help me clean up a few specific elements on my website. · ...

McKesson, l'une des 10 premières entreprises du classement Fortune Global 500, touche à pratiquement tous les aspects des soins de santé et s'emploie à faire une réelle différence. Nous sommes reconnus pour notre capacité à offrir un savoir, des produits et des services qui rende ...

We are seeking an experienced iOS developer to convert our existing Flutter source code into an iOS application. The candidate will be responsible for ensuring the app functions seamlessly on iOS devices and meets all Apple Store guidelines. Additionally, the developer will handl ...

+We are looking for an experienced Quality Assurance and Documentation Consultant to support Class II medical devices. · +Create QMS documentation templates SOPs. · Translate engineering materials into formal documents. · Prepare files for Class II devices software lifecycle docu ...

We have a React Native/Expo medication tracking app built on Rork AI that is approximately 85-90% complete. · We need an experienced developer to finalize the remaining items for App Store and Google Play submission. · ...

We are developing a sophisticated medical device that integrates Mechanical Design, Electrical Hardware, Firmware and AI Models. We are looking for a Quality/Regulatory specialist to audit our current project structure on OneDrive and reorganize it into a compliant Design History ...

We are seeking a skilled developer to transform our Google AI studio application into a fully functional Android app that can be installed locally on devices. This project does not require submission to app stores; we only need a standalone app that works seamlessly on Android de ...

We are developing an electronic circuit board intended for use in a regulated environment. To ensure compliance with ISO QMS for medical devices) and IEC medical device software lifecycle standard), we are seeking an experienced consultant to review our design and development app ...

Job summary · Drive Diagnostic Innovation – Join Us as a Regulatory Affairs Associate · Competitive Salary & 100% Employer-Paid Benefits · ...