- Terumo Neuro (Aliso Viejo, CA)
- …functionally with Associates across all departments in R&D, Operations, Quality, and Regulatory Affairs to achieve company objectives and resolve project issues. ... Minimum six (6) years of relevant work experience in medical device industry. 3. Minimum one (1)...product development and project management of embedded software/firmware for medical devices . 6. Knowledge of and ability… more
- University of Pennsylvania (Philadelphia, PA)
- …support. Ensure subjects are educated regarding the protocol specifics and study drugs/ devices . + Assist interventionalists in investigational device trials, ... escorting participants to other testing/procedure areas.. . Coordinate several investigational device trials in the cath lab, instruct and support investigators and… more
- AbbVie (Jersey City, NJ)
- …toxicology leads, regulatory and clinical development leads as well as medical affairs colleagues to help guide dose selection and regimen, ... for safety surveillance for pharmaceutical / biological / drug - device combined products + Lead and set the strategy...for key pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses and risk… more
- Abbott (Alameda, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... combination of appropriate education and experience. + Experience working on medical device studies and/or in-vitro diagnostics studies preferred. Pharmaceutical… more
- PCI Pharma Services (Rockford, IL)
- …shape the future of PCI. **Job Title: Senior Validation Engineer - Medical Device Assembly (CDMO)** **Location:** [Rockford] **Department:** Quality **Reports ... **Senior Validation Engineer** to support the validation activities associated with medical device assembly lines within a fast-paced Contract Development… more
- General Dynamics Information Technology (Fort Detrick, MD)
- …and medical and regulatory writing support for FDA-regulated drug, biologic, medical device , and combination products. **This is a PART TIME position (20 ... The Office of Regulated Activities (ORA) is a multidisciplinary team of regulatory affairs , compliance, and clinical support professionals dedicated to… more
- Abbott (Sylmar, CA)
- … Regulatory Compliance/ Affairs experience in In Vitro Diagnostics and medical device manufacturing or other similarly regulated environment. + Knowledge ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Rush University Medical Center (Chicago, IL)
- **Job Description** Location: Chicago, Illinois Business Unit: Rush Medical Center Hospital: Rush University Medical Center Department: Pediatrics-Res Adm **Work ... Neurology Research will be responsible for the overall fiscal, regulatory , operational, administrative, and personnel management of the Pediatrics Neurology… more
- Philips (Cambridge, MA)
- …the right fit if:** + You have a minimum of 15+ years' combined experience in Medical Device Clinical Research and Medical Device development within FDA ... Japan and China. + You have a detailed understanding of Clinical & Medical Affairs , leveraging expertise to propose innovative ideas, providing meaningful input… more
- Adecco US, Inc. (Southington, CT)
- …*Must be familiar with and comfortable using computers. *Working knowledge of the medical device regulatory procedures, lean manufacturing, and manufacturing ... Assembler - Medical Device Assembler, Operations - Adecco...quantity and good manufacturing practices to satisfy customer and Regulatory Affairs requirements. Read and/or understand operating… more