Position Description:Sr. Regulatory Affairs Specialist for Medtronic, Inc. Minneapolis, MN. Multiple positions available. Responsible for developing regulatory strategies, preparing U.S. and international submissions and obtaining and maintaining approval for products and therapies to markets worldw...
Cadena is looking for a Team Leader / Culture Specialist (Cat. I) for an EU FWC mission By: cadena | Published on: Mar 8, 2024 | Categories: | For the Lot 12 EU Framework Contract, Cadena is immediately looking for experts for the following mission: Assessment of PROCULTURA and identification / form...
Work Flexibility: Remote or Hybrid or OnsiteWe are currently seeking a Senior Regulatory Affairs Specialist to join our Trauma and Extremities EU MDR transition team to be based in Memphis, Tennessee or remotely anywhere within the United States. WHO WE WANT:• Dedicated achievers. People who thrive ...
**About Stryker**Stryker is one of the world's leading medical technology companies and, together with our customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hosp...
Great opportunity for REMOTE based Regulatory Affairs Specialist working with Medical Device! We are looking for RA Specialist to join our team in working with various Medical Device companies in REMOTE based work. Must have experience in Authoring 510k Submissions and well as FDA Submissions. All m...
An international medical device company is looking for candidates to remotely join their Regulatory Affairs team. The company encounters a lot of situations dealing with mergers, acquisitions and sell-offs of various products/business units. This role will be involved with determining the regulatory...
Our client, a world leader in Life Sciences who is looking for Regulatory Affairs Specialist II(100% Remote).Job Title: Regulatory Affairs Specialist II (100% Remote)Job Type: Long-Term ContractLocation: Santa Clara, CA Responsibilities:• Manages regulatory responsibilities associated with the devel...
Great opportunity for REMOTE based Regulatory Affairs Specialist working with Medical Device! We are looking for RA Specialist to join our team in working with various Medical Device companies in REMOTE based work. Must have experience in Authoring 510k Submissions and well as FDA Submissions. All...
Great opportunity for REMOTE based Regulatory Affairs Specialist working with Medical Device! We are looking for RA Specialist to join our team in working with various Medical Device companies in REMOTE based work. Must have experience in Authoring 510k Submissions and well as FDA Submissions. All...
In this exciting role as the Senior Regulatory Affairs Specialist (Sr. RAS) is responsible for planning and executing regulatory activities necessary to obtain and maintain regulatory approvals within the EU and International Regions. The Sr. RAS will provide support for regulatory activities includ...
In this role, you have the opportunity to Provide Regulatory support the company's Emergency Care and Resuscitation business products. With advance expertise and knowledge of regulatory requirements you’ll developed and drive regulatory strategies for high tech medical devices. You are responsible ...
Kelly Science & Clinical is currently seeking a Remote Regulatory Affairs Senior Specialist for a long-term engagement with one of our Global Med Device clients out of Raynham, MA***This role is fully remote*** This person will join our Kelly FSP (Functional Service Provider) division, a ma...
Job Description SummaryJob DescriptionBe part of something bigger!BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtu...
Required:Ability to update tech files or write tech docs for EU MDR.Class 3 device experience needed. Ability to answer deficiencies.FDA PMA and EU experience would be ideal.Candidate can work remotely anywhere in the US.Required Knowledge and Experience: Requires mastery of a specialty area and ful...
Required:Ability to update tech files or write tech docs for EU MDR.Class 3 device experience needed. Ability to answer deficiencies.FDA PMA and EU experience would be ideal.Candidate can work remotely anywhere in the US.Required Knowledge and Experience: Requires mastery of a specialty area and ful...
An international medical device company is looking for candidates to remotely join their Regulatory Affairs team. The company encounters a lot of situations dealing with mergers, acquisitions and sell-offs of various products/business units. This role will be involved with determining the regulatory...
A Remote Regulatory Affairs Specialist role in Cincinnati, Ohio is now available through Adecco Medical and Science. In this role, you will assume the responsibility for regulatory compliance of a portfolio of medical devices used with the organization's contrast media. The Regulatory Affairs person...
Edwards has a unique opportunity to join the Transcatheter Heart Valve (THV) Regulatory Affairs group, focused on developing solutions for patients suffering from structural heart disease.This role could be office based, in Irvine, California, or remote anywhere in the US.The THV clinical organizati...
Edwards has a unique opportunity to join the Transcatheter Heart Valve (THV) Regulatory Affairs group, focused on developing solutions for patients suffering from structural heart disease.This role could be office based, in Irvine, California, or remote anywhere in the US.The THV clinical organizati...
SUMMARY: The Senior Specialist, Regulatory Affairs provides project representation and input to projects awarded to WCT for all stages of the drug development cycle. RESPONSIBILITIES: Liaise with the Regulatory Affairs Manager/Regulatory Affairs Director to plan, organise, compile progres...
MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI...
Remote Sr. Regulatory Affairs Specialist Duration: Contract to hire Education & Qualifications:B.S. in a technical discipline preferred or equivalent experience.4+ years experience in Regulatory Affairs in the medical device industryExpertise in working within Medical Device Regulations including Qu...
A Remote Regulatory Affairs Specialist role in Cincinnati, Ohio is now available through Adecco Medical and Science. In this role, you will assume the responsibility for regulatory compliance of a portfolio of medical devices used with the organization's contrast media. The Regulatory Affairs person...
A Remote Regulatory Affairs Specialist role in Cincinnati, Ohio is now available through Adecco Medical and Science. In this role, you will assume the responsibility for regulatory compliance of a portfolio of medical devices used with the organization's contrast media. The Regulatory Affairs person...
Job Summary Zimmer Biomet Dental is a global leader in implant and restorative dentistry solutions with more than 60 years of industry experience. We are proud to be part of one of the largest musculoskeletal companies in the world. Our mission is to alleviate pain and improve the quality of life fo...
Remote Sr. Regulatory Affairs SpecialistDuration: Contract to hire Education & Qualifications:B.S. in a technical discipline preferred or equivalent experience.4+ years experience in Regulatory Affairs in the medical device industryExpertise in working within Medical Device Regulations including Qua...
**About Stryker**Stryker is one of the world's leading medical technology companies and, together with our customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hosp...
About Stryker Stryker is one of the world's leading medical technology companies and, together with our customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospita...
Job Description Responsibilities: Divisional Process Owner (DPO) for Medical Affairs procedures including authoring and revising standard operating procedures (SOPs) to meet all corporate and regulatory requirements. You are accountable for representing procedures in internal and external audits, re...
Our client, a Global Leader in the Medical Device Industry has an immediate opening for a Regulatory Affairs (RAQA) Documentation Specialist for a 12 month + Contract. Our client offers results-driven people a place where they can make a difference - every day! You will also have the opportunity to ...
Job Description SummaryJob DescriptionBe part of something bigger!BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtu...
Job DescriptionJob Title: MDR - Regulatory Affairs SpecialistLocation: Remote or Irvine, CA 92617Duration: 24 monthsHM Top needs:1. EU MDR support2. Medical device experience3. EU MDR/ Regulatory experience knowledge, Project management experience (even as a team member, not necessarily leader), Sav...
Regulatory Affairs Specialist/Senior - REMOTE - EUROPE Multiple Locations: United Kingdom • Poland • France • Belgium • Netherlands Requisition Number991Employment Type:Regular We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for ...
In this role, you have the opportunity to Support manufacturing location changes for Sleep & Respiratory Care and Hospital Respiratory Care. You are responsible for Coordinate and Manage Regulatory Timelines for projects / products shared across different business units Participate in review...
Job Description SummaryThe Staff Regulatory Affairs Specialist is responsible for developing strategies for moderately to highly complex submissions to regulatory agencies worldwide, and directly accountable for executing the US and EU registrations. This position is responsible to support new produ...
Role Overview:The Sr. Regulatory Affairs Specialist is responsible for preparing US and EU regulatory submissions and strategies as well as supporting International regulatory submissions and regulatory strategies for regions beyond US and EU. The incumbent possesses knowledge of regulatory requirem...
About StrykerStryker is one of the world's leading medical technology companies and, together with our customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...