- ConvaTec (Lexington, MA)
- …to 10 years of clinical trial management experience in conducting and leading global medical device clinical trials, preferably with a sponsor company. + Solid ... full-time Convatec CSMs). **Principal Contacts & Purpose of Contact** Internal - Medical Affairs , Clinical Operations (Study Management, Site Management, Data… more
- Actalent (Irvine, CA)
- …Quality organization. + Collaborate with cross-functional teams including Product Development, Regulatory Affairs , and Advanced Operations. + Participate in ... control processes. Required Qualifications: + Strong experience in document control and medical device regulations. + Proficiency in EU MDR, ISO standards,… more
- Exelon (Oakbrook Terrace, IL)
- …relationships with both internal and external stakeholders including, Engineering, Regulatory , Legal, Governmental Affairs , and unversities, national ... development and implementation of short and long term strategic initiatives. Support regulatory intiatives for new technology. (25%) + Manage the performance and… more
- Teleflex (Albany, NY)
- …an optimal customer experience. Collaborating with Marketing, Sales, Engineering and Clinical & Medical Affairs on key projects and initiatives, the CSS utilizes ... our Arrow (TM) brand of technically advanced vascular access devices are renowned throughout the world. Many of our...**Specialized Skills / Other Requirements** * 2+ years of Medical Device Industry experience. * 3+ years… more
- Takeda Pharmaceuticals (Boston, MA)
- …Takeda Oncology including Translational Medicine, Clinical Sciences, Global Regulatory Affairs , the Oncology Business Unit (Commercial and Medical Affairs ... and external diagnostic partners, and supporting health authority meetings and regulatory submissions (PMAs etc). This role will partner closely with key… more
- University of Pennsylvania (Philadelphia, PA)
- …involving neuroimaging, blood biomarkers, neuropsychological assessment, and pharmacological and device interventions. TBIRI is seeking a detail-oriented and dynamic ... neuropsychological assessments, MRI imaging sessions, and operating TMS-EEG and other devices . The ideal candidate should be detail-oriented and have prior… more
- Olympus Corporation of the Americas (Westborough, MA)
- …21 CFR 820 and ISO 13485 required. + Working knowledge of international medical device quality system requirements required. + Complete understanding and ... and early morning teleconferences. **Preferred:** + MBA Preferred. + Medical Device Experience preferred + Black Belt...Posting Notes: || United States (US) || Massachusetts (US-MA) || Westborough || Quality & Regulatory Affairs … more
- Vanderbilt University Medical Center (Nashville, TN)
- **Discover Vanderbilt University Medical Center** : Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, ... as issues arise or follow up on returned checks or payments not received. 11. Team devices - keeping track of laptops and iPads that our team has; will work with IT… more
- Medtronic (Newton, MA)
- …live case learning opportunities. + Collaborate with cross-functional teams, including R&D, regulatory affairs , and clinical teams, to ensure alignment on ... written and oral communication skills. + 2+ years of medical device or other regulated industry (such...a relevant field. + Certification in quality systems or regulatory affairs (eg, Six Sigma, ASQ, or… more
- Candela Corporation (Marlborough, MA)
- …improvement actions related feedback. . Jointly accountable with Quality System (QS) and Regulatory Affairs (RA) Leadership for ensuring the QS is effectively ... field, plus 15 years of related experience in the medical device industry with at least 12...12 years in a management/leadership role in quality / regulatory / compliance. . Working understanding of relevant global/regional… more