- Kelly Services (Springfield, MO)
- **Overview:** Our client is seeking a Contract Quality Engineer with medical device experience to support the successful implementation of ISO 13485 at our ... procedures and ISO expectations. **Required Experience:** + Proven experience in medical device manufacturing environments. + Hands-on implementation of ISO… more
- LSI Solutions (Los Angeles, CA)
- …in 1986, located in beautiful Victor, New York, is a dynamic and growing medical device company with over 500 employees dedicated to advancing minimally invasive ... passionate people looking to make a difference in the medical device industry. By joining LSI SOLUTIONS(R)...is ultimately the patient. POSITION TITLE : Surgical Sales Consultant - Los Angeles BASE SALARY RANGE: $50,000.00 -… more
- Guidehouse (Philadelphia, PA)
- …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
- Norstella (Columbia, SC)
- …world's leading providers of data and intelligence on clinical trials, drug treatments, medical devices and what's new in the regulatory and commercial ... Senior Solution Consultant Company: Citeline Location: Remote, United States Date...top 10 global pharma and CROs. From drug and device discovery and development to regulatory approval,… more
- Fujifilm (Carson City, NV)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... **Position Overview** The Senior Technical Clinical Consultant , Cardiology shall be responsible for all aspects...+ Ability to work effectively with customers in the medical field. + Ability to prioritize and handle multiple… more
- Guidehouse (New York, NY)
- …Guidehouse Life Sciences is an engine of innovation, helping pharmaceutical, biotech, medical device , and diagnostic companies develop custom solutions that ... to deliver product planning, pricing, reimbursement, product commercialization, and regulatory and compliance solutions. Consultants work with Guidehouse Life… more
- Guidehouse (New York, NY)
- …Guidehouse Life Sciences is an engine of innovation, helping pharmaceutical, biotech, medical device , and diagnostic companies develop custom solutions that ... to deliver product planning, pricing, reimbursement, product commercialization, and regulatory and compliance solutions. Senior Consultants are integral members of… more
- SHI (San Juan, PR)
- …**Job Summary** The Information Technology Spend Optimization (ITSO) Procurement Consultant is responsible for helping customers achieve cost savings through ... teams to ensure that all procurement activities adhere to legal and regulatory requirements. + Prepare, review, and revise customer contract templates, ensuring… more
- Guidehouse (Philadelphia, PA)
- …Life Sciences practice is an engine of innovation, helping pharmaceutical, biotech, medical device , and diagnostic companies develop custom solutions that tackle ... your DNA? Breakthroughs in pharma are helping people live healthier lives, while medical devices enable patients to proactively maintain health - this is undoubtedly… 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 ... your DNA? Breakthroughs in pharma are helping people live healthier lives, while medical devices enable patients to proactively maintain health - this is undoubtedly… more
- Chemours (Boston, MA)
- …Engineering, Biological Science, Toxicology or comparable technical field + 5+ years of medical device regulatory compliance experience with respect to raw ... outside lawyers, consultants, industry associations, and local agencies on specific medical regulatory topics. + Coordinate and review customer… 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
- Abbott (St. Paul, MN)
- …information from varied disciplines including Clinical Medicine, Engineering, Marketing and Regulatory Affairs required. Medical device industry experience ... data analysis, validation testing, and serving as a clinical consultant on clinical workflows and risk evaluation documentation. **What...or, Design Validation and GLP study experience in the medical device industry. + Demonstrated ability to… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …with technology solutions that will mitigate risk + Solid understanding of the medical device and healthcare IT space + Advanced analytical and problem-solving ... of possible!** BD is one of the largest global medical technology companies in the world. _Advancing the world...help BUs deliver best-in-class secure products, consistent with global regulatory requirements over the lifecycle. This role works in… more
- J&J Family of Companies (Santa Clara, CA)
- …CMS rule making process, and a legacy of strategy development within the medical device market. Experience with influencing private payor coverage policies is ... experience, with 7+ years of work experience in implantable medical device market access/reimbursement industry, with specific responsibility/experience… more
- Abbott (Abbott Park, IL)
- …inspection support. This support encompasses FDA inspections for the Nutrition, Medical Device , Diagnostics, and Pharmaceutical sectors within Abbott. **What ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Abbott (Boston, MA)
- …Experience** + Associate's degree required + 7 years of Cath Lab and/or Medical Device experience **Preferred Experience** + Bachelor's Degree highly preferred. ... and provides reporting information for reports submitted to the regulatory agencies. * Monitors adherence to protocols and determines...Development + Cath Lab Tech or Surgical Tech + Medical Device experience + OCT experience Please… more
- Edwards Lifesciences (Irvine, CA)
- … guidelines (eg, GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/ Medical Device research setting + Excellent problem-solving, organizational, analytical ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you… more
- Cardinal Health (Indianapolis, IN)
- …with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device ). + Experience with equipment qualification, software validation, test ... offers a wide variety of benefits and programs to support health and well-being. + Medical , dental and vision coverage + Paid time off plan + Health savings account… more
- HCA Healthcare (Manchester, NH)
- …Maintains appropriate inventory of all supplies. Ensures compliance with the Safe Medical Device Act. Human Resource Management: Maintains responsibility for ... of open and responsive communication among staff, ancillary departments, and medical staff, other department directors, providers, vendors, regulatory agencies,… more