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, ...
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...
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...
HOW MIGHT YOU DEFY IMAGINATION? You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and the passion you already have. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our beco...
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...
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...
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...
Regulatory Affairs Specialist Seeking a Regulatory Affairs Specialist who will be responsible for the preparation of regulatory submissions required to market or investigate new or modified medical devices in both domestic and international markets. This responsibility entails supporting the develop...
Regulatory Affairs Specialist Seeking a Regulatory Affairs Specialist who will be responsible for the preparation of regulatory submissions required to market or investigate new or modified medical devices in both domestic and international markets. This responsibility entails supporting the develop...
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 Subject to applicable law, all prospective hires will be required to demonstrate that they have been fully vaccinated for COVID-19 or intend to be vaccinated for COVID-19 by November 1, 2021, or qualify for a medical or religious accommodation to this vaccination requirement. Hir...
**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...
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 ...
**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 Description Summary** This position is part of a corporate project scheduled for a three-year contract term. This position works closely with the RA Leadership Team, and after the term of the project the candidate would be able to apply and move into a long-term position.**Job DescriptionBe part...
JOB SUMMARY: Remote work eligible except in Colorado and Connecticut. Under limited supervision, the Senior Regulatory Specialist is responsible for planning and executing critical and complex global regulatory projects necessary to obtain and maintain global regulatory approvals. Prepare comprehens...
JOB SUMMARY: Remote work eligible except in Colorado and Connecticut. Under limited supervision, the Senior Regulatory Specialist is responsible for planning and executing critical and complex global regulatory projects necessary to obtain and maintain global regulatory approvals. Prepare comprehens...
**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 SUMMARY: Remote work eligible except in Colorado and Connecticut. Under limited supervision, the Senior Regulatory Specialist is responsible for planning and executing critical and complex global regulatory projects necessary to obtain and maintain global regulatory approvals. Prepare comprehens...
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 ...
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...
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...
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...
Work Flexibility: Remote or Hybrid or OnsiteWe are currently seeking a Senior Regulatory Affairs Specialist to join Stryker's Robotics Division- Mako to be based in Weston, Florida or remotely anywhere within the United States.Who we want Meticulous documenters. Detail-oriented people who enjoy main...
**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...
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...
**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 Description Summary****Job Description****Be 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 prese...
Responsibilities: Identifies regulatory pathways for initial product designs and provides input to internal stakeholders Provides strategic input and technical guidance on global regulatory requirements to product development Assesses all requirements and potential obstacles for market acc...
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...
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...
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...
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...
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...