- Takeda Pharmaceuticals (Lexington, MA)
- …product. The Staff Device Engineer has extensive experience in medical devices for drug delivery including combination products, solid understanding of ... of my knowledge. **Job Description** **Primary** **Role:** The Staff Device Engineer will lead technical efforts for...polymeric medical device manufacturing processes via molding and… more
- Abbott (Burlington, MA)
- …of FDA regulations and guidance, ISO 13485, ISO 14971, Software Standards (eg, 62304), EU Medical Device Regulations and MDSAP + Experience with medical ... their health and get on with their lives. We are seeking an experienced Staff Engineer , Software Design Quality to ensure our medical devices are developed in… more
- Bausch Health (Bothell, WA)
- …tests. Lead / participate in Design and Code reviews Demonstrated experience with Medical Device System/SW verification for Windows CE based devices and Embedded ... compliant to EN IEC 60601-1 /-2:, EN IEC 62304: Medical Device Directive Essential Requirements. Working experience...a sales incentive plan. Benefits package includes a comprehensive Medical (includes Prescription Drug ), Dental, Vision, ,… more
- Gilead Sciences, Inc. (Foster City, CA)
- … Engineer to lead technical development efforts for parenteral drug - device combination products, including autoinjectors, prefilled syringes, and needle ... safety systems. This individual contributor role is ideal for an engineer with deep technical expertise, strong cross-functional collaboration skills, and a passion… more
- Walmart (Bentonville, AR)
- **Position Summary ** **What you'll do ** Join Walmart as **Principal, Software Engineer - Enterprise Device Management** in our Global Technology team. Your ... **About the Role | Team** The team is focused on developing an Enterprise Device Management platform that integrates with any device type to enhance management,… more
- GRAIL (Durham, NC)
- …management system (QMS). This role's focus is on the in vitro diagnostic medical device processes, supporting the clinical laboratory processes as needed with ... regular on-site presence (5 days a week) **Responsibilities:** + Support medical device Quality Engineering operations through expert interpretation,… more
- Jabil (West Chester, PA)
- …tools. + Certification in Quality Engineering (eg, CQE) is a plus. Benefits + Medical , Dental, Prescription Drug , and Vision Insurance with HRA and HSA options ... around the globe. How will you make an impact? As a Quality Engineer , you will support key quality systems, ensure compliance with internal and regulatory… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …true to the best of my knowledge. **Job Description** **Title: Senior/Principal Engineer , Combination Products and Drug Delivery Devices** **Location: Cambridge, ... MA** **About the role:** As a Senior/Principal Engineer , Combination Products and Drug Delivery Devices, you will provide project and technical leadership in the… more
- University of Utah (Salt Lake City, UT)
- …dedicated to shaping the future of patient care through medical device innovation. As Principal Biomedical Engineer , you'll collaborate with visionary ... rates based on their business need and budget.** **Responsibilities** ** Medical Device & Equipment Engineer ,...the successful completion of a criminal background check and/or drug screen._ _The University of Utah values candidates who… more
- PCI Pharma Services (Bedford, NH)
- …discipline. + **Experience** - 10+ years in engineering/facilities/utilities (preferably biotech, medical device , or pharmaceutical). + **Technical Expertise** - ... future of PCI. We're looking for a **hands-on, highly skilled Principal Process Engineer ** to lead complex engineering projects from concept to completion. In this… more
- BD (Becton, Dickinson and Company) (Irvine, CA)
- …in control theory, signal processing, physiological systems, and algorithm development for medical device innovation. This is a critical role in shaping ... in control theory, signal processing, physiological systems, and algorithm development for medical device innovation. This is a critical role in shaping… more
- Global Foundries (Essex Junction, VT)
- …GLOBAL FOUNDRIES is seeking highly skilled and motivated semiconductor process development engineer to join our Fab9 Technology Development team to develop and ... Essex Junction, Vermont (Fab9). As a Lead Epitaxy development engineer you will be responsible to design and develop...etc). + Define and optimize III-V superlattices, buffers, and device layers and requirements as defined in the Technology… more
- Stryker (San Jose, CA)
- …** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SiMD) or Software in a Medical Device (SiMD) ... strong technical skills + Experience with regulatory agencies (FDA, MoH, TUV) and medical device regulations (820, IEC 62304/82304, 60601), with experience in… more
- Amgen (Cambridge, MA)
- …automate model creation and post/processing. + Experience with combination products and device regulatory requirements, medical device development and design ... and transform the lives of patients while transforming your career. **Senior Engineer : Mathematical Modeling and Simulation** **Cambridge, MA** **What you will do**… more
- DEKA Research & Development (Manchester, NH)
- …a Product Complaints Engineer - Team Lead to work in a dynamic Medical Device Research and Development environment. The position reports to the Product ... / other regulatory requirements. + Identify and make sound decisions regarding medical device reporting to regulatory agencies. + Interface with Third… more
- Integra LifeSciences (Plainsboro, NJ)
- …policies, US Food and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical Device Regulations ... set new standards of care. The **Sr. Q** **uality Engineer / Quality Operations (Validations, Risk Management & Statistics)**...Drug Administration (FDA) regulations, ISO 9001, ISO 13485:2003, Medical Device Directive (MOD), the Canadian … more
- Lilly (Indianapolis, IN)
- …A minimum of 2 years of work experience in GMP regulated pharmaceutical and/or medical device industries is required. + Background in sterile barrier and/or deep ... Eli Lilly and Company supports the design, development, and commercialization of drug products and pharmaceutical delivery systems including medical devices and… more
- ManpowerGroup (Savannah, GA)
- Our client, a leading organization in the medical device manufacturing industry, is seeking a dedicated and experienced Quality Engineer to join their team. ... 7-10 years of experience in quality engineering within the medical device industry. + Significant experience with...completion of waiting period consultants are eligible for:** + Medical and Prescription Drug Plans + Dental… more
- BD (Becton, Dickinson and Company) (Sparks, MD)
- …methods is required. Familiarity with Design Control requirements and knowledge of Medical Device Validations is preferred. **Education and Experience:** + ... **Job Description Summary** The Quality Engineer II is responsible for the application and...Control, or Product/Process non-conformance investigations + Experience in a medical device or pharmaceutical manufacturing facility. +… more
- System One (Houston, TX)
- …insurance, etc.) + 401k after 30 days + Job offer will be contingent on drug screen and background check Position Synopsis: Engineer VI, I&C will be relied ... Instrumentation and Control (I&C) Engineer VI 100% Remote System One is seeking...system functionality, developing control system architectures, and defining I/O device interfaces. The position includes managing budget, scope schedule… more