/ Experience Requirements 2+ years of Medical Device Industry experience. 3+ years of experience in a business environment... with Marketing, Sales, Engineering and Clinical & Medical Affairs on key projects and initiatives, the CSS utilizes critical thinking...
. DESIRED EXPERIENCE, CERTIFICATIONS & PROFESSIONAL AFFILIATIONS 2+ years of Medical Device Industry experience. 3+ years... with Marketing, Sales, Engineering and Clinical & Medical Affairs on key projects and initiatives, the CSS utilizes critical thinking...
, Clinical and Medical Affairs, Legal/Compliance, Regulatory, and other key departments. The individual will also be expected... Marketing Communications Clinical and Medical Affairs Legal Regulatory Corporate Brand Management and Communications...
rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19... require them. The specialist will maintain the Master Control document management system, ensure compliance with regulatory...
to 5:00 PM. No travel required. Preferred: Minimum of 2 years of experience in a medical device company or equivalent... (US-WA) || Redmond || Quality & Regulatory Affairs (QA/RA)...
to 5:00 PM. No travel required. Preferred: Minimum of 2 years of experience in a medical device company or equivalent... (US-WA) || Redmond || Quality & Regulatory Affairs (QA/RA)...
, medical device, or consumer goods industry....Job Summary: The Regulatory Labeling Specialist/Manager is responsible for managing and overseeing the development...
Pharmacology for the U.S. East Coast Hub. Will interact with Medical Specialists, Clinical Operations, Medical writing, Regulatory..., Data Science (statistics, pharmacometrics), Research and Early Development, Global Translation, Global Medical Affairs...
with Medical Specialists, Clinical Operations, Medical writing, Regulatory, Data Science (statistics, pharmacometrics), Research... and Early Development, Global Translation, Global Medical Affairs, Global Safety (GS), Bioanalysis, CMC and occasionally...
pharmaceutical, biotechnology, or medical device industry. Familiarity with quality management systems (QMS) and electronic... Assurance, Regulatory Affairs, and Data Management, to ensure successful validation activities. Provide training and guidance...
, including IT, Quality Assurance, Regulatory Affairs, and Data Management, to ensure successful validation activities. Provide... validation processes through the use of data analytics and automation. Stay updated with industry best practices, regulatory...
. Strong organizational skills and attention to detail. Experience in the pharmaceutical, biotechnology, or medical device industry...: Work closely with cross-functional teams, including IT, Quality Assurance, Regulatory Affairs, and Data Management...
affairs, or regulatory affairs (optional) in the medical device or pharmaceuticals industry Advanced analytical skills... most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing...
affairs, or regulatory affairs (optional) in the medical device or pharmaceuticals industry Advanced analytical skills... most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing...
-functional partners such as Laboratory Operations, R&D, Regulatory, Medical Affairs, etc. to ensure timely document reviews... within a regulated environment Experience working in electronic document management systems Experience working in a medical device...
Assurance or Regulatory Affairs activities in a cGMP Medical Device or Pharmaceutical environment 5+ years of Demonstrated... "Diagnostics Specialist." Why Join Diasorin? Impactful Work: When you join Diasorin, you become part of a team that's dedicated...
Handling Procedure. The Quality Specialist will perform the evaluation of customer complaints for Medical Device Report (MDR... preferred). Experience in the medical device industry, pharma and/or highly supervised industry is preferred. A qualified...
Procedure. The Quality Specialist will perform the evaluation of customer complaints for Medical Device Report (MDR...). Experience in the medical device industry, pharma and/or highly supervised industry is preferred. A qualified auditor of ISO...
complaints process. Quality Specialist is responsible for processing and closing all medical device/IVD, product safety... a CE/IVD or FDA supervised company preferred). Experience in the medical device industry, pharma and/or highly supervised...
certification preferred. Regulatory Affairs Certificate (Medical Device/Pharmaceuticals) or equivalent experience strongly desired... to the CDMO industry, such as intellectual property, regulatory requirements, and commercial laws. Compliance and Risk...