Eu Mdr - 25+ job offers

Riverpoint Medical in Portland Oregon is looking to hire a Regulatory Affairs Associate (EU MDR Submissions) . At Riverpoint you will be part of the process that brings great technology to Medical, Dental and Veterinary markets. We specialize in the design and manufacturing of premium medical device

Company Description Global Regulatory Writing & Consulting (GLOBAL) specializes in providing expert consulting, regulatory submission support, and strategic writing services for the pharmaceutical and medical device industries. The company focuses on delivering tailored, high-quality solutions t

Planet Pharma

A leading healthcare company is seeking a knowledgeable regulatory affairs specialist with expertise in medical devices. The role includes managing regulatory submissions and ensuring compliance with FDA and EU standards. Candidates should have at least 3-5 years of relevant experience and a Bachelo

IntePros

A healthcare consulting firm in Minneapolis is seeking a Sr Regulatory Affairs Specialist. The role involves preparing regulatory submissions, interfacing with agencies, and ensuring compliance with medical device regulations. Ideal candidates should have a Bachelor’s degree and 3-5 years of relevan

Redbock - an NES Fircroft company

A leading medical device firm is seeking a Sr. Regulatory Affairs Specialist for a 24-month contract. This role involves coordinating regulatory submissions and impacting assessments for medical devices with a focus on US FDA and EU MDR. Candidates should have 3-5 years of experience, preferably wit

Position: EU MDR Quality Engineer - Onsite Location: Franklin Lakes, NJ Duration: 12 Months Total Hours/week: 40.00 Shift: 1st Shift Client: Medical Devices Company Job Category: Engineering/Technical Level of Experience: Mid-Level Employment Type: Contract on W2 (US Citizens, Green Card Holders, EA

E-Solutions

Title: Verification & Validation Engineer with EU MDR, TMV Location: Southington, CT JD: 5+ years' experience in working with the Medical devices Experience in EUMDR Remediation & FDA regulations Hands On Experience in Test Method Validation (TMV) Explicit experience in Design Controls (Inpu

A health technology company is seeking a Principal Regulatory Affairs Specialist in San Diego, CA. The role requires a minimum of 8 years in FDA regulated environments and expertise in 510(k) and EU MDR compliance. You will lead regulatory strategies, provide guidance to cross-functional teams, and

A health technology company is seeking a Principal Regulatory Affairs Specialist in San Diego, CA. The role requires a minimum of 8 years in FDA regulated environments and expertise in 510(k) and EU MDR compliance. You will lead regulatory strategies, provide guidance to cross-functional teams, and

Overview Contract Duration: 12 months – Estimated to end: 3/2027 (Contract Extension Expectation) Location : 100% ONSITE - Mahwah, NJ (07430) Type : W2 contract (NO C2C OR THIRD PARTY will be considered for this role) Work Authorization: Must be currently in the United States with active employment

A medical technology company is seeking a Quality Engineer to prepare technical documentation for regulatory compliance. The role involves reviewing Design History Files and collaborating with various departments to ensure adherence to EU MDR requirements. Ideal candidates will have a Bachelor's deg

A leading engineering firm is seeking a high-caliber engineer to lead the strategic implementation of 2D barcode solutions for EU MDR compliance in Mahwah, NJ. The engineer will develop validation strategies, design validation protocols, and ensure compliance with labeling requirements. Candidates s

A regulatory consulting firm is seeking a Sr. Regulatory Affairs Specialist for a 24-month contract with flexible location options. The role requires extensive medical device regulatory experience, particularly with US FDA and EU MDR regulations. Candidates should hold a Bachelor's degree in life sc

Akkodis

Akkodis is seeking a Remote Medical Device EU MDR Project Manager for a 12+-month job with a client in Bloomington, IN.You will provide subject matter expertise in defining scope of project and determining project methodology, resource allocation and facilitation based on project needs.Rate Range :$

A leading medical technology company is seeking a Principal Clinical Evaluation Medical Writer in Mounds View, MN. This full-time role involves authoring clinical and scientific documents, analyzing clinical evidence, and creating responses for regulatory queries. Candidates must possess a Master's

A leading medical technology company is seeking a Risk Management Engineer to support Design Quality Assurance and EU MDR remediation initiatives. The ideal candidate will collaborate cross-functionally to ensure compliance with standards, develop and remediate risk management and usability document

International Medical Industries, Inc.

A well-established medical device organization in Florida is looking for a Regulatory Affairs Specialist to support regulatory compliance activities. The role involves preparing and maintaining regulatory documentation, supporting audits, and ensuring products meet U.S. and international regulatory

Riverpoint Medical

A leading medical device company in Portland, Oregon, is seeking a Medical Writer to support clinical evaluations and report writing. The ideal candidate will have an advanced degree in a scientific or medical discipline, with 2-3 years of experience specifically in clinical evaluation reports. Resp

A health technology company is seeking a Principal Regulatory Affairs Specialist in Colorado Springs. This role involves ensuring compliance with US FDA, EU, and international regulations for medical devices. The ideal candidate should have over 8 years of experience in regulatory affairs within FDA

A leading staffing firm is seeking a QA/RA Project Manager for a 24-month+ project focused on the implementation of EU MDR for its Surgical Innovation unit. The role requires extensive experience in regulatory affairs, project management, and strong communication skills. The chosen candidate will ma