As a part of the Tenet and Catholic Health Initiatives family, Conifer Health brings 30 years of healthcare industry expertise to clients in more than 135 local regions nationwide. We help our clients strengthen their financial and clinical performance, serve their communities and succeed at the bu...
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...
HOW MIGHT YOU DEFY IMAGINATION?If you feel like youre part of something bigger, its because you are. At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies. We are global collaborators who achieve togetherresear...
Risk Analyst needed in Chichester £15.33ph PAYE - Reference:RQ(phone number removed)Please note that this role will be working from home, until easing of COVID restrictions1. Demonstrable practical experience in analysing, interrogating and interpreting a wide range of highly complex information fro...
You've been building to this for a long time. Now, here's an opportunity that will bring all your study, all your training, your certifications and your energy to a new level as you develop solutions to transform the health care industry as a key player with Optum and UnitedHealth Group. As a VP of ...
You've been building to this for a long time. Now, here's an opportunity that will bring all your study, all your training, your certifications and your energy to a new level as you develop solutions to transform the health care industry as a key player with Optum and UnitedHealth Group. As a VP of ...
Description: Associate Director OR Senior Associate Director, CMC Regulatory Affairs "Candidate to be hired at level commensurate with experience" CMC Regulatory Affairs professional who is responsible for global and/or U.S. CMC regulatory support of New Chemical Entities. Define CMC regulatory...
Job Summary:Today, our Medicare Advantage business is administered on multiple legacy core technology platforms that lack automation and do not support all its business requirements. This results in an unfavorable administrative cost position and an overly complex operating model that, if not addres...
You've been building to this for a long time. Now, here's an opportunity that will bring all your study, all your training, your certifications and your energy to a new level as you develop solutions to transform the health care industry as a key player with Optum and UnitedHealth Group. As a VP of ...
Job Description SummaryJob DescriptionThis position is responsible for the preparation of regulatory submissions required to market new or modified medical devices in both the U.S. and Europe, and related regulatory affairs activities, such as development, execution and management of procedures and ...
Description: Associate Director OR Senior Associate Director, US Regulatory Lead (Cardiovascular / Metabolic) Remote ***Candidate will be hired commensurate with the level and experience*** Associate Director Description\: With supervision for assigned development projects and US marketed ...
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...
Education:Bachelor's Degree, and three years of relevant experience. Five or more years preferred.Experience:Three years of experience in a training role; Health Plan or PBM experience; E-learning experience helpful. Requires high level of initiative and creativity, as well as intermediate to expert...
Job Description SummaryJob DescriptionSr. Regulatory Affairs Project Manager - Software - REMOTEReporting to Sr. Regulatory Affairs Director NPD, the Sr. Regulatory Affairs (RA) Project Manager is responsible for providing software and cybersecurity regulatory leadership to obtain US and OUS product...
Careers that Change Lives In Surgical Innovations, we advance minimally invasive surgery to improve outcomes for patients and providers around the globe. From concept to commercialization, we bring meaningful innovation to our robust and growing portfolio of surgical devices and technologies. Throug...
Locum Consultant in Public Health (Health Care Public Health)Minimum of 6 monthsFully remoteCompetitive daily ratePanoramic Associates are working with a Local Authority who is seeking a Locum Consultant in Public Health to assist in Health Care Public Health. This position can be fulfilled fully re...
Title:Government Compliance Specialist - Remote OptionKBR Government Solutions delivers full life cycle professional and technical solutions that improve operational readiness and drive innovation. Our solutions help ensure mission success on land, air, sea, space and cyberspace for the Department o...
Spec, Regulatory Affairs - Sr- Remote Work - Monday to Friday JOB SUMMARY:Provide regulatory guidance in product design, clinical studies, market authorization strategies, labeling, advertising, and product withdrawals and recalls. Provide pre-market and post-market regulatory strategy and implement...
Spec, Regulatory Affairs Sr- Remote Work - Monday to FridayJOB SUMMARY:With minimal supervision, responsible for coordination and preparation of document packages for regulatory submissions from all areas of the company. Compiles all materials required for submissions, license renewals and annual re...
Spec, Regulatory Affairs - Sr- Remote Work - Monday to Friday JOB SUMMARY:Provide regulatory guidance in product design, clinical studies, market authorization strategies, labeling, advertising, and product withdrawals and recalls. Provide pre-market and post-market regulatory strategy and implement...
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...
Our client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools is looking for u201cRegulatory Affairs Manager(100% Remote) u201d.Job Title: Regulatory Affairs ManagerJob Type: Long Term Contract(Possibility Of Extension)Job Responsibilities:• Manages regulatory responsibilities a...
Description Government Underwriter - Local and Remote Opportunities available! Attractive Signing Bonus!Local and non local candidates experienced with working remote are encouraged to apply! Positions require ability to work a Pacific Standard Time Standard Schedule.Who we are:Summit Funding is a p...
Job Description SummaryJob DescriptionThe Staff Regulatory Affairs Specialist is responsible and accountable for developing and executing sound strategies for regulatory submissions and registrations for complex new product development projects. This position interfaces with multiple projects and fu...
Pacific Scientific Energetic Materials Company (PacSci EMC), a Fortive Corporation (NYSE: FTV) operating company, makes critical missions possible. From concept to demonstration to delivery, we provide leading-edge energetic materials, devices and subsystems for use in military and commercial applic...
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...
Stryker is one of the world's leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgi...
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...
Job Responsibilities:Responsible for regulatory project deliverables, timelines and submission activities for new product development (NPD) or sustainment projectsLead regulatory activities for NPD projects including planning, preparing and submitting regulatory submissionsManage, guide, coach and l...
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...
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 SummaryJob DescriptionThe Staff Regulatory Affairs Specialist is responsible and accountable for developing and executing sound strategies for regulatory submissions and registrations for complex new product development projects. This position interfaces with multiple projects and fu...
Role OverviewThe role will be part of a collaborative and energetic team working on a highly pivotal initiative for Smith+Nephew and provides an exciting opportunity for someone to innovate and optimize processes as well as contribute to a high impact project within the medical device industry.As a ...
Stryker is one of the world's leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgi...
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...
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges...
Role OverviewThe role will be part of a collaborative and energetic team working on a highly pivotal initiative for Smith+Nephew and provides an exciting opportunity for someone to innovate and optimize processes as well as contribute to a high impact project within the medical device industry.As a ...
Company DescriptionBio-TechJob DescriptionRemote OR may sit at any client site, manager works in EST but open to candidates in different time zonesTitle: Regulatory CMC ManagerJob Description: Assist in the development of module 3 templates that will enable population by automation tools, and enable...
Overview Iovance seeks a highly motivated Senior Regulatory Operations Specialist. The successful candidate has substantial experience planning and managing regulatory authority submissions. The Senior Specialist will ensure the compilation of compliant and timely regulatory submissions in eCTD form...
UnitedHealthcare is a company that's on the rise. We're expanding in multiple directions, across borders and, most of all, in the way we think. Here, innovation isn't about another gadget, it's about transforming the health care industry. Ready to make a difference? Make yourself at home with us and...