Requisition ID: 48259 Title: Senior Specialist, Regulatory Affairs - Medical Device Imaging Systems and SaMD Division: Arthrex, Inc. (US01) Location: Inc- Work From Home (US11)Position Summary: Arthrex, Inc. is a global medical device company and a leader in new product development and medical educa...
Hillrom is a $2.8B leading worldwide manufacturer and provider of medical technologies and related services for the health care industry, including patient support systems, safe mobility and handling solutions, non-invasive therapeutic products for a variety of acute and chronic medical conditions, ...
Requisition ID: 48259 Title: Senior Specialist, Regulatory Affairs - Medical Device Imaging Systems and SaMD Division: Arthrex, Inc. (US01) Location: Inc- Work From Home (US11) Position Summary: Arthrex, Inc. is a global medical device company and a leader in new product development and medical...
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 ...
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...
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 ho...
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 ...
Job Description : Senior Staff Regulatory Affairs Specialist is responsible for creating and executing regulatory strategies and objectives in alignment with business needs. This includes the preparation of regulatory submissions required to market new or modified medical devices in the U.S. an...
At Cepheid, we are passionate about improving health care through faster, more accurate diagnostic tests. As a member of our team, you’ll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission drives us, every mom...
Our client, a growing Pharma company focused in Oncology, is looking for a Director/Sr. Director, Regulatory Affairs, CMC. This position will be 100% Remote. This position is responsible for developing and implementing CMC regulatory strategies to facilitate the progress of R&D drug development a...
Our client, a growing Pharma company focused in Oncology, is looking for a Director/Sr. Director, Regulatory Affairs, CMC. This position will be 100% Remote. This position is responsible for developing and implementing CMC regulatory strategies to facilitate the progress of R&D drug development a...
Our client, a growing Pharma company focused in Oncology, is looking for a Director/Sr. Director, Regulatory Affairs, CMC. This position will be 100% Remote. This position is responsible for developing and implementing CMC regulatory strategies to facilitate the progress of R&D drug development a...
Our client, a growing Pharma company focused in Oncology, is looking for a Director/Sr. Director, Regulatory Affairs, CMC. This position will be 100% Remote. This position is responsible for developing and implementing CMC regulatory strategies to facilitate the progress of R&D drug development a...
Our client, a growing Pharma company focused in Oncology, is looking for a Director/Sr. Director, Regulatory Affairs, CMC. This position will be 100% Remote. This position is responsible for developing and implementing CMC regulatory strategies to facilitate the progress of R&D drug development a...
Our client, a growing Pharma company focused in Oncology, is looking for a Director/Sr. Director, Regulatory Affairs, CMC. This position will be 100% Remote. This position is responsible for developing and implementing CMC regulatory strategies to facilitate the progress of R&D drug development a...
Responsibilities: Evaluate the regulatory environment and provide internal advice throughout the product lifecycle for marketed devices to ensure product compliance. Anticipate regulatory obstacles and emerging issues throughout the product lifecycle and develops solutions. Assist in the develo...
Requisition ID: 48218 Title: Specialist II, Regulatory Affairs - Medical Devices Division: Arthrex, Inc. (US01) Location: Inc- Work From Home (US11) Position Summary: Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. ...
Requisition ID: 48218 Title: Specialist II, Regulatory Affairs - Medical Devices Division: Arthrex, Inc. (US01) Location: Inc- Work From Home (US11)Position Summary: Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex...
Director, Medical Affairs/Clinical Science (Remote, US) Transcatheter Mitral and Tricuspid TherapiesEdwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring with a rapidly growing portfolio of inno...
Director, Medical Affairs/Clinical Science (Remote, US) Transcatheter Mitral and Tricuspid TherapiesEdwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring with a rapidly growing portfolio of inno...
Director, Medical Affairs/Clinical Science (Remote, US) Transcatheter Mitral and Tricuspid TherapiesEdwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring with a rapidly growing portfolio of inno...
Director, Medical Affairs/Clinical Science (Remote, US) Transcatheter Mitral and Tricuspid TherapiesEdwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring with a rapidly growing portfolio of inno...
**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...
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...
Work Flexibility: Remote or Hybrid or OnsiteWe are currently seeking a Senior Regulatory Affairs Specialist to join our Biologics team on the Trauma & Extremities Division to be based in Memphis, TN or remotely anywhere in the United States.Who we want Collaborative partners. People who build and le...
**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...
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...
EUROIMMUN US is an MDSAP registered, ISO 13485:2016, 21 CFR 820 compliant Medical device company that develops, manufactures, distributes, and performs service and installation activities of in vitro diagnostic test kits, instruments and software used in the detection of autoimmune status, allergies...
Job Title: Associate Director/Director, Regulatory Affairs CMC - RemoteThe Position: This organization is looking for a Regulatory CMC leader to apply experience and leadership to their Regulatory Affairs CMC team. You will be responsible for the overall management of a portfolio of biological produ...
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...
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...
**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...
Our client, a growing Pharma company focused in Oncology, is looking for a Director/Sr. Director, Regulatory Affairs, CMC.This position will be 100% Remote.The Director/Sr. Director, Regulatory Affairs, CMC will also serve as a regulatory specialist on select project teams. Responsibilities:&nb...
**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...
Wondering what’s within Beckman Coulter Diagnostics? Take a closer look. At first glance, you’ll see that for more than 80 years we’ve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be...
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...
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...
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...
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...
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...