- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …technical discipline required (eg, engineering, bioengineering, biology, chemistry). + Minimum 5 years Regulatory Affairs experience in medical device or in ... has the unique opportunity to be involved with both medical devices and in vitro diagnostics, allowing...regulatory authority personnel (eg FDA, Notified Bodies) in medical device and in vitro diagnostic areas.… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …US, EU, and other global regulatory requirements are met. + Evaluates medical device regulations and leads development of global regulatory strategies ... and evaluate proposed device changes. The Sr. Regulatory Affairs Specialist is able to interpret...4 years Regulatory Affairs experience in the medical device industry preferred **Preferred Qualifications:** +… more
- Robert Half Technology (Mahwah, NJ)
- …will play a crucial part in managing document-related changes while ensuring compliance with regulatory standards for medical devices . This is a long-term ... and learning management systems. * Solid understanding of quality assurance principles and regulatory requirements for medical devices . * Experience in… more
- Medtronic (New York, NY)
- …understanding of regulatory requirements and industry standards governing medical device reprocessing. + Excellent communication, interpersonal, and ... Standards such as St-79, 58, and other pertaining to medical devices reprocessed in hospital settings. **Nice...upholding the highest standards of safety and quality in medical device reprocessing. + This position is… more
- Otsuka America Pharmaceutical Inc. (Queens, NY)
- …**Experience & Qualifications** + A minimum of 2 years of pharmaceutical or medical device sales experience. + Must reside within a commutable distance ... with a focus on pharmaceutical products to meet unmet medical needs and nutraceutical products for the maintenance of...In Otsuka's evolved customer engagement model, a Neuroscience LTC Specialist will engage HCPs through a variety of in-person,… more
- Kelly Services (Mahwah, NJ)
- …document related changes in accordance with change management procedures and relevant regulatory requirements for medical devices . This role will ... **Document/Change Management Specialist ( NO C2C or Third Party)** +...+ Basic knowledge and understanding of US and International Medical Device Regulations. + Ability to plan,… more
- Amgen (Yonkers, NY)
- …years of sales and/or marketing experience within pharmaceutical, biotech, healthcare, or medical device industries. + Product or hospital sales experience in ... us and transform the lives of patients while transforming your career. **Senior Oncology Specialist ** **What you will do** Let's do this. Let's change the world. In… more
- Stryker (Mahwah, NJ)
- …Publications Specialist , you will play a key role in ensuring our medical device labeling is clear, compliant, and accessible, supporting safe and effective ... teams and external partners to deliver high-quality documentation that meets global regulatory standards and enhances patient safety. To learn more about Stryker's… more
- Sanofi Group (New York, NY)
- …**Qualifications** + BA / BS degree required + 3+ years of pharmaceutical, biotech or medical device sales experience + Account Management sales and / or rare ... **Job Title:** Therapeutic Specialist Tzield, New York, NY **Location:** US Remote/Field...as directed + Maintaining strict adherence to all legal, regulatory , ethical, administrative, and financial duties + Achieving and… more
- Guidehouse (New York, NY)
- …in your DNA? Breakthroughs in pharma are helping people live healthier lives, while medical devices enable patients to proactively maintain health - this is ... Life Sciences practice is an engine of innovation, helping pharmaceutical, biotech, medical device , and diagnostic companies develop custom solutions that tackle… more