- Medtronic (Mansfield, MA)
- …+ Design Dossier and/or Technical Documentation experience + Technical Writing + International medical device regulatory submission/approval experience, to ... conducting regulatory change assessments, and supporting the implementation of the EU Medical Device Regulation (MDR). The Sr. RAS translates regulatory… more
- ZOLL Medical Corporation (Boston, MA)
- …PhD, or equivalent) is preferred. Experience : + 5+ years of clinical or medical device /pharmaceutical industry experience. Required. + 7+ years of experience in ... collaborative, with a proven ability to work effectively across functions such as medical , marketing, sales , and product development. + Ability to drive results… more
- Abbott (Burlington, MA)
- …types of product complaints. Independently assesses the complaint to determine if a medical device report needs to be filed with various global regulatory ... of related work experience **Preferred Qualifications** + Knowledge of global regulations for medical device reporting and medical terminology is a plus… more
- Sanofi Group (Cambridge, MA)
- …capacity. + Deep expertise in Oncology, strongly preferred. + Expertise in international Device regulation as well as market implementation strongly preferred ... **Job Title:** Global Medical Affairs Director - Oncology **Location:** Cambridge, MA...blood disorders, cancers, and neurological disorders. From R&D to sales , our talented teams work together, revolutionizing treatment, continually… more
- ThermoFisher Scientific (Boston, MA)
- …clinical business development and key account management in a related Pharmaceutical, Biotech or Medical Device sales industry + Experience in global ... the exciting challenge of developing and executing a strategic sales plan to maximize business from your assigned global...and **_deep industry knowledge across the pharmaceutical, biotech, or medical device sectors_** , along with a… more
- Philips (Cambridge, MA)
- …design changes, and field safety corrections, with a primary focus on Software as a Medical Device (SaMD) for our Sleep & Respiratory Care products in the US, ... a minimum of 7+ years' experience in Regulatory Affairs/Strategy within FDA regulated Medical Device environments. + You have proven expertise in Software as… more
- Teradyne (North Reading, MA)
- …powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device ... on our flagship UltraFLEXplus tester + Value Proposition Development: Collaborate with Sales , Product Development, and the Marketing team to create a compelling… more
- Teradyne (North Reading, MA)
- …powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device ... power requirements, test cell footprint, test head form factor, ESG initiatives, device interface technology, and beyond. Key Responsibilities + Strategic Vision &… more
- Fujifilm (Boston, MA)
- …manager, senior product manager, product/technical director). + Minimum 8 years of medical device experience with strong clinical background. + Prior experience ... with various stakeholders internally and externally (eg, healthcare professionals, sales & field personnel, global R&D, operations, regulatory, global marketing,… more
- Candela Corporation (Marlborough, MA)
- …Degree in engineering or related field, plus 15 years of related experience in the medical device industry with at least 12 years in a management/leadership role ... quality / regulatory / compliance. . Working understanding of relevant global/regional medical device regulations and standards with particular emphasis on… more