- 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
- NTT DATA North America (Newark, NJ)
- …apply now. We are currently seeking a IT Sales -Managed Services/Life Sciences-Med- Device (Remote) to join our team in Newark, New Jersey (US-NJ), United ... in digital, cloud and automation across a comprehensive portfolio of consulting , applications, infrastructure and business process services. This is primarily a… more
- Quality Consulting Group (Juncos, PR)
- …in engineering (preferably) + 5+ years of relevant experience + Experience in medical device design, development & manufacturing. + Experience of products with ... advantage. + Proven project execution. + Hands on experience on Projects/Scheduling for Medical Device manufacturing. + Critical thinking and PM skills. (eg… 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
- Penn Medicine (Philadelphia, PA)
- …working with medical hardware, software and equipment products + Understand medical device usage within a health system environment + Experience working ... for low, medium and high risk equipment, utilizing a strong understanding of medical device integration and networking. + Correctly and efficiently applies basic… more
- Penn Medicine (Philadelphia, PA)
- …for low, medium and high risk equipment, utilizing a strong understanding of medical device integration and networking. Correctly and efficiently applies basic ... with tasks that have been mastered. Uses understanding of Regulatory and Safety requirements to communicate Biomed compliance to... medical hardware, software and equipment products Understand medical device usage within a health system… more
- General Dynamics Information Technology (Fort Detrick, MD)
- …of education, professional training, or work experience. + 5 years of related medical or regulatory writing experience. + Experience writing investigational new ... Execution **Skills:** eCTD,Investigational New Drug Application (IND),New Drug Application (NDA), Regulatory Documents, Regulatory Writing **Experience:** 5 + years… 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
- Abbott (Plymouth, MN)
- …types of product complaints + Independently assesses the complaint to determine if a medical device report needs to be filed with various global regulatory ... information into the complaint database; independently determining and filing appropriate medical devices reports with various regulatory agencies; participating… more