A company is looking for a Medical Device Reporting (MDR) Specialist for a 3-6 month remote contract.Key Responsibilities : Handle MDR filings and ensure timely and accurate submission to regulatory bodiesMake determinations on whether incidents require MDR reporting based on regulatory criteriaInvestigate and analyze adverse events related to medical devicesRequired Qualifications : Proven experience in medical device reporting and regulatory complianceStrong understanding of MDR processes and regulatory requirementsProficiency in relevant reporting tools and softwareAbility to work independently and manage multiple tasks effectivelyStrong organizational skills
Medical Device Reporting Specialist
A company is looking for a Medical Device Reporting (MDR) Specialist for a 3-6 month remote contract. ...
Senior Regulatory Affairs Specialist
A company is looking for a Senior Regulatory Affairs Specialist, Medical Devices. ...
Regulatory Affairs Specialist
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....
Senior Regulatory Affairs Specialist
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...
Regulatory Affairs Specialist - Contractor
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 ...
Regulatory Affairs Specialist
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 (remote)
Medical manufacturer is hiring a Regulatory Affairs Specialist on a temporary basis. Previous medical device experience in a Regulatory Affairs capacity . ...
Regulatory Affairs Specialist 3.
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...
Senior Specialist, Regulatory Affairs, Critical Care
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...
Account Specialist (Work from home)
We're looking for candidates with great customer service skills to fill our Remote Customer Service role!.This role is entirely remote and offers full-time/Part time hours with flexibility .We are ready to schedule interviews for this week.We're seeking someone who is great with people, building rel...