- Eliassen Group (Marlborough, MA)
- …subsystems and systems. . Create design documentation to support medical device product development in alignment with regulatory requirements and industry ... **Mechanical Engineer- R&D, Medical Device ** **Marlborough, MA** **Type:** Contract.... Collaborate with cross-functional teams, including R&D, clinical, and regulatory , to review documentation and specifications to ensure alignment… more
- Trinity Health (Muskegon, MI)
- …time **Shift:** **Description:** Coordinator needed to help regionalize the Cardiac Device Management program. Ensures quality and regulatory compliance related ... of evidence-based practice education and competencies. * Ensures quality and regulatory compliance related to cardiac device standards using project… more
- Element Materials Technology (Fairfield, OH)
- **Overview** Element has an opportunity for an *on-site* ** Medical Device Project Engineer** to join our rapidly expanding team in Fairfield, Ohio. This position ... scheduling, testing , data analysis and reporting. The Project Engineer will manage medical device testing projects, using standard and custom test frames across… more
- Cognizant (Chicago, IL)
- …Global Pharmaceutical market and industry, including BioTech, Medical Device , Traditional Rx, enabling technologies and regulatory /compliance in the ... **Experience Partner - Life Sciences (Pharma / BioTech / Medical Device )** **Associate Director - Chicago/Midwest Remote**...to plan and run existing clients. You'll work with Consulting and other parts of Cognizant like Data, and… more
- IQVIA (Washington, DC)
- …guidelines, and apply these to services provided. * Stay current on US medical device regulatory requirements. Qualifications: * Bachelor's degree required; ... years of consulting or client facing experience preferred; direct healthcare and/or medical device experience preferred. * Should understand medical … more
- Abbott (Burlington, MA)
- …various types of product complaints. Independently assesses the complaint to determine if a medical device report needs to be filed with various global ... + 5 years related work experience **Preferred Qualifications** + 3+ years in MDR ( Medical Device Reporting) + Knowledge of the use, development, and … more
- Cook Medical (Bloomington, IN)
- …in experimentation and foster a culture of statistical rigor in our medical device development and manufacturing environments. Responsibilities + Lead ... initiatives, and collaborate across global teams to uphold Cook Medical 's commitment to quality excellence and regulatory ...testing , and method validation + Strong knowledge of medical device regulations (ISO 13485, 21 CFR… more
- Gilead Sciences, Inc. (Foster City, CA)
- …communication skills are required. + Demonstrated ability to facilitate the interface with medical device vendors and HF consulting firms. + Demonstrated ... aspirations. Join Gilead and help create possible, together. **Job Description** The Device , Packaging and Process (DPP) function is a key component of Gilead's… more
- Guidehouse (Chicago, IL)
- …Life Sciences practice is an engine of innovation, helping pharmaceutical, biotech, medical device , and diagnostic companies develop custom solutions that tackle ... value, access, pricing and commercialization strategy projects for pharmaceutical, biotechnology, medical device , and diagnostics companies. Our client services… more
- embecta (Parsippany, NJ)
- …Quality, the Sr. Manager of Design Assurance, will lead and build a dynamic medical device design assurance team focused on standardizing and deploying best in ... class processes that include the design and development of embecta's diabetes care medical device worldwide. This person will lead the engagement and interaction… more