- Nissha Medical Technologies (Sandpoint, ID)
- …not required) **Knowledge, Skills & Abilities** + Previous related industry experience in medical device production is preferred but not required. + Ability to ... - 1:30 am. This is a full-time position. _Nissha Medical Technologies is committed to fair, competitive, and market-informed...the Manager. + Responsible for the quality of the product produced. + Works well with various internal and… more
- Dentsply Sirona (Milford, DE)
- …Experience: + 5(+) years of experience in regulatory affairs, preferably in the medical device industry. + Experience with leading regulatory submissions and ... and providing guidance to their direct reports and cross-functional product development teams on US and EU regulatory requirements....13485, EU MDR). + Experience with software as a medical device , AI and/or medical … more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …Technical Files, etc.) + Develop and implement global regulatory strategy for MMS Dispensing Medical Device and non- Medical device products and software ... a Regulatory Affairs standpoint. Support will consist of new product development, sustaining, and end of life activities. The...to comply with new and existing regulations (eg, FDA Medical Device Regulations, EU-MDR) + Support the… more
- AbbVie (Florham Park, NJ)
- …position is responsible for the operations and strategic design of the US Medical Device & Aesthetics businesses global supply planning organization which ... support very significant revenue streams for Medical Device & Aesthetics businesses. Achieving the...demand into inventory and replenishment plans to meet the product needs of our customers and patients, developing short… more
- Abbott (St. Paul, MN)
- …for second shift. This position is responsible for the packaging of high-quality medical device hardware and systems. Each employee can make a difference ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Bausch + Lomb (Greenville, SC)
- …US Class II/Class III medical devices, as well as non-US medical device regulations, applicable sterile drug/aseptic processing regulations experience in the ... In-depth knowledge of applicable regulations and standards, both domestic and international ( medical device or drug). Proven technical and problem-solving skills… more
- Abbott (Pleasanton, CA)
- …cross-functional project teams** to drive supplier quality initiatives, ensuring alignment with medical device regulatory standards (eg, FDA, ISO 13485). + ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Medtronic (FL)
- …required + Minimum of 3 years of field sales experience **Nice to Have** + Medical Device sales experience + Capital sales experience + GI experience + ... The Senior TM will serve as a customer facing product expert primarily responsible educating physicians and nurses on...in Microsoft Office: Power point, Excel, and Word. + Medical device /equipment sales experience. + Experience selling… more
- J&J Family of Companies (Irvine, CA)
- …2 years of quality, manufacturing, or research and development experience in a medical device or other regulated industry **SECTION 4: REQUIRED KNOWLEDGE, ... years of quality, manufacturing, or research and development experience in a medical device or other regulated industry. **Experience and Skills:** **Required:**… more
- Fujifilm (Phoenix, AZ)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... marketing organization. The incumbent is responsible for supporting the product management group including, but not limited to market...with a Master's degree. + Minimum 10 years of medical device industry experience in a clinical… more