- BHI Energy (Reno, NV)
- …hire position. If you have at least 1 or more years assembler experience in the medical device field or a related technical field, then this may be the right ... devices in accordance with released manufacturing documentation. + Provide support as required in all phases of product...+ 1 or more years assembler experience in the medical device field or a related technical… more
- Actalent (Austin, TX)
- …standards, and customer requirements. The primary function is to support the product release department by reviewing device history and batch records for ... This role is focused on bolstering throughput for the Product Release department. Responsibilities + Review device ...for this temporary role may include the following: * Medical , dental & vision * Critical Illness, Accident, and… more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... products/services targeted by the organization . Provide coaching, advice, support , motivation or information to help individuals meet and.... Proven track record of leading sales in the medical device or disposable device … more
- Abbott (Pleasanton, CA)
- …Ensure all test strategies and practices align with medical device regulatory standards (FDA, ISO, IEC 62304). Support documentation, verification, and ... to define and implement comprehensive test automation strategies for Abbott's next-generation medical device software portfolio (Class II and Class III devices).… more
- Bausch + Lomb (Clearwater, FL)
- …and industry best practices. This includes the development, manufacturing and release of medical device product . KEY ACTIVITIES / RESPONSIBILITIES **Micro ... operational excellence and innovation. + 10-15 years of microbiology experience in biopharmaceutical/ medical device industry of which minimum of 5 years is… more
- Edwards Lifesciences (Irvine, CA)
- …Else We Look For (Preferred)** : + Degree in scientific discipline + Medical Device , Pharma, or Biotechnology industry experience + ISO 13485:2016 certification, ... on process improvement/remediation projects and responses from international affiliates + Support FDA device listings, establishment registrations and the State… more
- Abbott (Orlando, FL)
- …relevant technical field, engineering) or equivalent/related experience. + 7+ years clinical medical device experience or equivalent, ideally with CRM products. ... and present effectively written and verbal communications. + Thorough familiarity with medical device industry policies, operations and procedures. + Expert… more
- Hologic (Newark, DE)
- …3+ years with PhD). + Proven success leading high-performing test engineering teams in medical device product development. + Strong track record managing ... complex test projects, meeting budgets and deadlines. + Experience with medical device manufacturing and regulatory requirements (FDA, FAA, SEC, etc.). +… more
- Philips (Plymouth, MN)
- …if:** + You have a minimum of 5+ years' experience in FDA regulated medical device environments, with a focus on Design Assurance/Control, detailed knowledge of ... the QMS related to Design/Process Controls. + You have strong understanding of Medical Device QSR regulations/standards including ISO 13485, ISO 14971, 21CFR… more
- Teradyne (Sunnyvale, CA)
- …powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device ... major, world-class customer. This role involves driving the development of customer device test solutions in close collaboration with both the customer and… more