- Boston Medical Center (Boston, MA)
- $15,000 Sign On Bonus (external candidates only) Registered Respiratory Therapist-ECMO Specialist Boston Medical Center (BMC) is more than a hospital. It's a ... pump, tubing, artificial oxygenator, and related equipment. The ECMO Specialist , under qualified medical direction and supervision,...personnel to meet identified needs as documented by problem reporting and QI system. Manages work time in a… more
- Edwards Lifesciences (Boston, MA)
- …understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting Aligning our overall business ... (RT), Operating Room Technician (ORT), or Cardiovascular Technician (RCIS) or related medical device , clinical, or Certification in RDCS (Registered Diagnostic… 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. ... more than 160 countries. **Job Title** **Principal Field Clinical Specialist ** **Working at Abbott** At Abbott, you can do...Development + Cath Lab Tech or Surgical Tech + Medical Device experience + OCT experience Please… more
- Hologic (Marlborough, MA)
- …you passionate about ensuring the highest standards of quality and compliance in the medical device industry? We are seeking a dedicated and dynamic **Clinical ... Clinical QA Specialist Newark, DE, United States Marlborough, MA, United...understanding of FDA Quality System Regulations, ISO 13485, EU Medical Device Regulation, and ISO 14971 standards.… more
- Canon USA & Affiliates (Boston, MA)
- …Word, Excel, Oracle, Sales Force, etc. + 2 Years Regulatory Affairs experience in medical device industry required + Minimum Education Level: 2 Year / ... **Regulatory Affairs Specialist - Post Market - req1434** **OVERVIEW** Reporting to the Director Regulatory Affairs, the Regulatory Affairs Specialist is… more
- Takeda Pharmaceuticals (Lexington, MA)
- … device products + Knowledge of EU/ FDA cGMP requirements of drug/ device product complaints reporting and investigation + Desirable experiences: combination ... Description** **About the role:** As the Senior Quality Complaints Specialist , you will ensure the quality of processes and...US based employees may be eligible to participate in medical , dental, vision insurance, a 401(k) plan and company… more
- Fujifilm (Boston, MA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... **Position Overview** The Sales Specialist , Diagnostic Oncology, in the Invitro Diagnostics Division,...reporting (Salesforce.com) + Where appropriate, collaborate with the Medical Affairs Team. + Follow up to define pathway… more
- CGI Technologies and Solutions, Inc. (Boston, MA)
- **IT Lab Support Specialist - SME** **Category:** Business Analysis (functional and technical) **Main location:** United States, Massachusetts, Boston **Position ... . **Position Description:** CGI is seeking a SME IT Lab Support Specialist to join our growing team supporting life science clients through end-to-end… more
- Abbott (Boston, MA)
- …spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. Our 109,000 colleagues… more
- Cardinal Health (Mansfield, MA)
- …Services Center perform laboratory testing to characterize the chemistries of our medical device products and stability testing for pharmaceutical products of ... protocols utilizing specialized instrumentation and analytical techniques to characterize medical devices, materials, and processing aids for chemical properties of… more
- Cardinal Health (Mansfield, MA)
- …Services Center perform laboratory testing to characterize the chemistries of our medical device products and stability testing for pharmaceutical products of ... protocols utilizing specialized instrumentation and analytical techniques to characterize medical devices, materials, and processing aids for chemical properties of… more
- Zimmer Biomet (Braintree, MA)
- …Expect** Maintain Site Quality programs to ensure compliance to domestic and international medical device regulations. **How You'll Create Impact** + Develop and ... pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by… more
- Mentor Technical Group (Boston, MA)
- …the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, ... a Data Analyst, Data Engineer, or in a similar role involving analytics and reporting . + Proficiency in SQL, Python, Tableau, Power BI, or similar data analysis and… more
- Medtronic (Boston, MA)
- …implements aspects of the Surgical Operating Unit's (SOU) Post-Market Risk Management of medical device products or software systems. * May develop, evaluate, ... Life of a Post-Market Risk, Quality Engineering Manager - reporting to Director of Post-Market Risk, Surgical Operating Unit....SKILLS OR EXPERIENCE * Risk Management experience in the medical device industry * Risk Management File… more
- NTT America, Inc. (Boston, MA)
- …as well as requirements related to general safety, accident avoidance and reporting , personnel protective equipment, and job specific awareness. + Reviews project ... expenses associated with working remotely and use of a personal mobile device , if applicable. NTT Global Data Centers Americas, Inc. offers competitive compensation… more
- Fujifilm (Boston, MA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... **Position Overview** The Digital Radiography Sales Specialist is the regional DR and CT expert...account activity, quote activity, contact management, assets and result reporting is accurately populated in system. + Complies with… more
- Fujifilm (Boston, MA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... through the closing of business. + Work with the Clinical Sales Specialist in coordinating the pre-demonstration (pre-demo)process required to ensure that a… more
