- Abbott (Maple Grove, MN)
- …**Preferred** **Qualifications** + Advanced degree + 2-5+ years' experience in medical device or pharmaceutical clinical research studies. + Experience ... healthcare , with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000...working on medical device clinical studies in highly regulated… more
- Abbott (San Diego, CA)
- …debuggers, unit test frameworks) + Knowledge of design controls and regulations for medical device development is a plus + Understanding of quality software ... visual modeling, multi-threading, formal development methodologies, and source code management + Medical device product development knowledge is a plus + Ability… more
- Medtronic (Fridley, MN)
- …interactive and insightful reports and dashboards using Power BI + Experience in the medical device industry + Experience with 19 Code of Federal Regulations (19 ... can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down… more
- Pegasystems (Pittsburgh, PA)
- …, with demonstrable experience working with large health systems, pharmaceutical companies, medical device manufacturers, and healthcare payers across both ... (AWS, Azure, GCP), security, and governance principles-with specific knowledge of healthcare compliance requirements is a significant plus. * Excellent… more
- Fujifilm (Frankfort, KY)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... measurement/data mapping for project and or post go-live support cases in compliance with the company's quality procedures. **Company Overview** At FUJIFILM … more
- AbbVie (Austin, TX)
- … medical terminology, ability to pronounce medical terms + Knowledge of medical device , pharmaceutical market or related field + Experience in the ... aides, and quality metrics to build lasting relationships with Healthcare Practices across the nation. Our team is searching...with policies and procedures set by the program and compliance guidelines to grow prescription volume + Establish phone… more
- J&J Family of Companies (Irvine, CA)
- …+ Minimum of 6 years of relevant experience in clinical research within Medical Device or Pharmaceuticals, with demonstrated expertise in statistical design, ... clinical trial design, analysis plans, and reporting, ensuring scientific rigor, regulatory compliance , and strategic alignment in support of device evidence… more
- J&J Family of Companies (Cincinnati, OH)
- …lead the development and execution of toxicology and biocompatibility evaluations for surgical medical device products. This role will be pivotal in expanding ... Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where...toxicology/biocompatibility, with a strong focus in the pharmaceutical or medical device industries. + Board Certification in… more
- Stryker (Portage, MI)
- …environment. Preferred: + Previous experience in a regulated environment. Experienced in Medical Device manufacturing with strong familiarity in ISO 13485, GDP, ... + Knowledge or certification in GD&T preferred + Understanding of Med Device manufacturing processes Health benefits include: Medical and prescription drug… more
- Lilly (Concord, NC)
- …inspection. + Knowledge of current Good Manufacturing Practices (cGMPs) + Pharmaceutical, medical device or food processing industries + Manufacturing Execution ... to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to… more