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...
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, ...
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 ...
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...
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...
Are you passionate about making a difference in healthcare? Do you thrive in a dynamic, fast-paced environment? We're seeking a dedicated individual to join our team as a Clinical Trial Drug Supply Specialist. In this role, you'll play a pivotal part in supporting groundbreaking clinical trials that...
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 ...
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...
**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...
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...
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...
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...
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...
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...
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...
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...
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...
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...
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...
**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 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...
Hamlyn Williams have partnered with an established global online gaming/sports betting company to bring on a Director of Government Affairs to manage all governmental affairs, public policy initiatives, and drive influence to align with the company's business interests. In this role you will:...
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...
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...
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...
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...
**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...
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...