- DivIHN Integration Inc (Atlanta, GA)
- …so 2-5 years of experience is acceptable. Industry experience, medical device Background in Electro-Mechanical devices are flexible Regulatory experience is ... inputs (including but not limited to: Field Corrective Action (FCA), Complaints, FDA Medical Device Reports (MDR), etc.) to determining trends and systemic… more
- DivIHN Integration Inc (Medina, NY)
- …as assigned III. QUALIFICATIONS, KNOWLEDGE, AND SKILLS REQUIRED Experience in the medical device industry in development and deployment of Quality Systems, ... standardize inspection methods. Promote and train personnel to ensure awareness of regulatory and customer requirements throughout the company. Act as a technical… more
- DivIHN Integration Inc (Deerfield, IL)
- …and timely communication and reporting from multiple projects and quality/ regulatory Core Team members Meeting participation/facilitation Quality Management Systems ... Not task oriented able to be able to work to find answers Med device /Pharma/Regulated industry preferred but open to other industries for the right person as for… more
- Fisher Associates (Syracuse, NY)
- …but not limited to, the decision to use or access a particular drug, device , or medical service), marital status, partnership status, caregiver status, domestic ... Environmental Regulatory Specialist Syracuse, NY (http://maps.google.com/maps?q=120+East+Washington+St.+Syracuse+NY+USA+13202) * Environmental Job Type Full-time… more
- Publicis Groupe (New York, NY)
- …Saatchi & Saatchi Wellness has provided consumer and professional marketing, strategic consulting , and medical education to pharmaceutical and wellness brands. ... submissions follow the protocols established by our pharmaceutical and medical /surgical device clients for promotional materials. This...PM and Account teams as they prepare projects for Medical Legal Regulatory (MLR) review + Submit… more
- University of Rochester (Rochester, NY)
- …Initiatives, continually modify, as necessary, current quality systems to comply with the Medical Device regulation (21 CFR Part 820) and the European Commission ... direct and oversee implementation and ongoing compliance with the Medical Device Regulations through the establishment of...+ At least 8 years of Quality Assurance and/or Regulatory experience in the pharmaceutical or device … more
- Guidehouse (New York, NY)
- …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
- Globus Medical, Inc. (Audubon, PA)
- …experience in finance, consulting or investment banking preferred + Healthcare or medical device experience not required but a definite plus + Engineering ... horsepower and transaction experience to help execute a growing medical device company's strategic plan. As a...understand the idea or opportunity + Engage IP & Regulatory teams in the assessment of new technology with… more
- ThermoFisher Scientific (Wilmington, NC)
- …(especially peri- or post-approval late phase interventional studies) Medical device development (in-vitro diagnostics, SaaMD) Post-authorization ... winning project work related to pregnancy and lactation studies through scientific consulting . Understand the regulatory context for RWE specifically related to… more
- Olympus Corporation of the Americas (Westborough, MA)
- …Fellowship Trained Board Certification. + Minimum of 10-12 years of biotechnology/pharmaceutical/ medical device industry experience in medical affairs, ... Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can fulfill… more
- Abbott (Abbott Park, IL)
- … regulatory requirements. Work effectively with multiple different divisions and medical device technologies. Relies on extensive experience and judgment to ... ideal. + Minimum 10 years in Progressive work experience in software related medical device or high technology industries. Minimum 10 years prior management… more
- Precise Solutions (Lake County, IL)
- …Description: Primarily responsible for representing QA on cross-functional Software as a medical device (SaMD) and Digital Health Software product development ... ensure products are developed, tested, and released in compliance with worldwide Medical Device Regulations. Responsible for authoring, reviewing, and approving… more
- Olympus Corporation of the Americas (Westborough, MA)
- …microbiological liaison, data analytics, epidemiological investigative principles, medical device /technology product evaluation, performance improvement, ... prevention experience with patient safety, including hospitals, academia, health systems, medical device and/or pharmaceutical manufacturers. + Domestic and… 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 ... provides commercialization strategy and reimbursement services to pharmaceutical, biotechnology, medical device , and diagnostics companies. Our client services… more
- Medtronic (Detroit, MI)
- …M&T Structural Heart Business is one of the fastest growing businesses in the medical device industry and expanding rapidly to serve patients globally. The ... drive healthcare forward and remain a global leader in medical technology and solutions. To learn more about Inclusion...be assigned. + Conducts on-site education and / or consulting . + Supports field personnel in providing the best… more
- ZOLL Medical Corporation (Pittsburgh, PA)
- …innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and ... (https://cardiacdiagnostics.zoll.com/products/heart-failure-arrhythmia-management-system/) (Heart Failure Management system) is a non-invasive, patch-based device that monitors pulmonary fluid levels and has been… more
- KPMG (Charlotte, NC)
- …Qualifications: + Minimum ten to fifteen years of QMS experience in the Medical device , consulting and/or business experience or combination thereof ... in the Quality domain within the Life Science industry (Pharmaceutical, Medical Device , BioTech and Clinical Research Organization), experience with Trackwise… more
- Guidehouse (New York, NY)
- …Life Sciences practice is an engine of innovation, helping pharmaceutical, biotech, medical device , and diagnostic companies develop custom solutions that tackle ... study. + 3-5 years of Life Sciences (Pharmaceutical, Biotech, Specialty Pharma and/or Medical Technology) consulting experience is required. + Minimum 1 + years… more
- Highmark Health (Pittsburgh, PA)
- …to meet clinical and operational needs by providing the evaluation and research of medical device interoperability with other medical devices and/or IT ... Systems Engineering + Solid working knowledge of healthcare technology management, medical device and software interoperability and integration, hardware… more
- Abbott (Sylmar, CA)
- …Supply Chain groups in EPO Manufacturing Sites and in Affiliates. + Pharma/ Medical Device commercial, development, and manufacturing business process knowledge, ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more