- Gilead Sciences, Inc. (Parsippany, NJ)
- …. Works collaboratively with Clinical Operations, Formulation Process Development, Device Development and Clinical Package Engineering, Quality Assurance, ... Gilead, you will further our mission to address unmet medical needs and improve life by advancing the care...Escalates to senior leadership as needed . Partners with Quality Assurance to resolve quality -related issues with… more
- Fujifilm (Trenton, NJ)
- …or processes. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... must have expert level knowledge in all areas of medical informatics, IT infrastructure design and deployment, medical...with MI Project Management (PM) team to deliver high quality Synapse product solutions. + Act as primary technical… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …of 5-8 years project management experience. + Experience in medical device industries required, including experience in FDA or other regulated environments ... Description** We are **the makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the world of health (TM) is our… more
- Fujifilm (Trenton, NJ)
- …as assigned. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... with Key Accounts and Opinion Leaders within the Liver/Hepatology Medical Oncology community. Manage specific assigned geographic areas and successfully… more
- Sokol Materials & Services (Skillman, NJ)
- …+ Knowledge of biotech, bulk drug substance or finished product manufacturing, medical device analytical testing ishighly desirable. + Extensive knowledge of ... GXP with at least 8 years focused on product quality . Preferred Active member of ASQ or ISPE. +...Proven attention to details + Comfortable working in an FDA regulated environment. About the Role DUTIES AND RESPONSIBILITIES:… more
- J&J Family of Companies (New Brunswick, NJ)
- …meta-analyses + Evaluate the relevance and reliability of new data sources for medical device studies, including product-specific studies of J&J devices + ... launches, value assessments, predictive analytics, machine learning, and business development of medical devices. We are also applying AI tools in RWE analyses,… more
- Fujifilm (Trenton, NJ)
- …and procedures. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... Knowledge Base articles. + Maintains an expert working knowledge of current medical imaging products and related technologies. + Engineers must have the ability… more
- Sanofi Group (Morristown, NJ)
- …**About You** **Experience:** + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs + Successful track record of **relevant ... and company activities. + Assists in ensuring product support relationships with FDA are established and maintained. + Provides input into the global organization… more
- Abbott (Jersey City, NJ)
- …spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues ... you dream of. + Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO...Our business purpose is to restore health and improve quality of life through the design and provision of… more
- Fujifilm (Trenton, NJ)
- …and procedures. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... the business, to work on customer systems. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all job… more