- Olympus Corporation of the Americas (Westborough, MA)
- …matter expertise, technical guidance, and leadership for the application of health and medical device SW regulatory standards to the Olympus SDLC, including IEC ... on regulations around health software development, and software for medical devices . + Collaborate on the update...+ Minimum of 6 years of experience in a medical device setting. + Experience in the… more
- BD (Becton, Dickinson and Company) (Sparks, MD)
- …Validation involvement - such as a quality advisor/approver + Familiarity with medical device regulations and working in a regulated environment + Preferable ... **Job Description Summary** The Quality Engineer II is responsible for...required. Familiarity with Design Control requirements and knowledge of Medical Device Validations is preferred. **Education and… more
- Medtronic (Plainfield, IN)
- …Service & Repair team with a focus on spare part/accessory manufacturing and some device manufacturing. Service of medical devices is crucial to ensuring ... Change Lives** In this exciting role as a Manufacturing Quality Engineer II, you will be a...Experience with creation and completion of change controls. + Medical devices or Pharma experience. + Bachelors… more
- Terumo Medical Corporation (Elkton, MD)
- … Corporation (TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high- quality medical devices used in a broad range of ... of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in...robust manufacturing processes into the Value Streams The Senior Engineer 1 ensures technical quality , contributes to… more
- Medtronic (Minneapolis, MN)
- …primary responsibilities include overseeing all phases of cyber security life cycle of medical devices . These include proactive initiates to identify, model, and ... of cyber security frameworks, architectures for connected systems. Experiences in medical devices , FDA guideline and international standards (eg NIST,… more
- Integra LifeSciences (Plainsboro, NJ)
- …Certifications: ASQ CQE preferred + Experience: 6 to 8 years of experience in a Quality Assurance role for medical device or pharmaceutical manufacturing. + ... set new standards of care. The **Sr. Q** **uality Engineer / Quality Operations (Validations, Risk Management...and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical… more
- Cook Medical (Bloomington, IN)
- Overview The Quality Engineer at Cook Inc. serves as the lead quality representative of certain product lines within product development, manufacturing, ... clinical, and regulatory affairs.* Provide leadership in the understanding of medical device regulations and best practices* Manage conflict resolution… more
- Actalent (Sacramento, CA)
- …play a crucial role in ensuring the quality and compliance of new medical device products throughout their development lifecycle. You will be responsible for ... Job Title: Design Quality Engineer II For immediate consideration,...Thorough knowledge of US and International Medical Device Regulations. + Strong knowledge of Quality … more
- Actalent (Watertown, CT)
- …Essential Skills + Quality engineering + Quality assurance + Audit + Medical device expertise + CMM programming + GD&T + Statistical analysis + Root ... Job Title: Quality Engineer For immediate consideration, please...all testing processes and product developments comply with relevant medical device regulations such as FDA (21… more
- Actalent (Maple Grove, MN)
- …system. This position requires a background in the medical device industry, particularly in cardiological devices , including implantable heart valves ... Senior Quality EngineerJob Description The Senior Manufacturing Quality Engineer is a key member of...professional experience. + 8+ years of experience in the medical device industry with 3 to 5… more