standards across releases. Comply with regulatory requirements and documentation standards for Medical Device IT systems (e.g... lifecycle and developer mindset. Excellent problem-solving and debugging skills. Experience in Medical Device IT industry...
Device Quality Experience Strong experience in process quality or manufacturing quality within a regulated medical device...Job Title: SR Quality Engineer Job ID: 23382 Location: 2001 West Client Way, Tempe Arizona 85281-5133 Duration: 12...
. Experience in a medical device or similarly regulated environment Knowledge in equipment control systems, PLC (Beckhoff... is searching for a Sr. Mechanical Engineer to help design and construct manufacturing equipment to support production of Intuitive...
in a medical device process and/or product development environment. Hands-on experience with design verification/validation, risk... about driving quality improvements and ensuring the safety and reliability of life-changing medical devices? At Hologic...
Regulations, Medical Device Regulation, and ISO 13485 Quality Standards Requisition ID: 620578 Minimum Salary: $ 69500... - whatever your ambitions. About This Role: This Quality Engineer II role will provide support for Capital Equipment production operations...
. As a Data Quality Automation Engineer, you'll design and build intelligent validation systems that work across multiple project... data standards (HL7, FHIR) Experience with medical device data What Success Looks Like First 30 Days Ship your first...
in a medical device or similarly regulated environment Hands-on experience in establishing equipment specification, validation... is searching for a Mechanical Engineer to help design and construct manufacturing equipment to support production of Intuitive...
(s) related to medical device quality systems and/or production and process control or equivalent. Understanding of regulations... - whatever your ambitions. About the role: The Principal Quality Systems Engineer supports the development and maintenance of Global quality...
to lead technical problem solving as well as continuous improvement projects Previous Medical Device industry or other highly... regulated device manufacturing Experience completing validation activities including IQ/OQ/PQ, process characterizations...
product lifecycle to ensure medical devices (Class I and II) are safe and effective for use. This engineer will collaborate... with cross-functional project teams to improve product designs (new and existing), specifically the device user interfaces...
Demonstrated ability to team well with other engineers and scientists. Preferred: Medical Device industry experience..., is currently recruiting for a Principal Reliability Engineer to join the Ethicon team! At Johnson & Johnson, we believe health...
years of experience in relevant field(s) related to medical device quality systems and/or production and process control... or equivalent. Understanding of medical device regulations and standards applicable to the BSC Global Quality System and Process...
: Experience in the medical device industry Project management experience Experience with validation and qualification... business unit. Boston Scientific ranked #2 among medical device companies on Forbes America's Best Places to Work...
and compliance activities within the medical device or pharmaceutical environment. This role focuses on regulatory adherence, risk... Required Qualifications 3 5 years of hands-on experience in Quality Engineering within medical device or pharmaceutical manufacturing...
(s) related to medical device quality systems and/or production and process control or equivalent. Understanding of regulations... – whatever your ambitions. About the role: The Principal Quality Systems Engineer supports the development and maintenance of Global quality...
’s leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide and operations in more than 160... manufacturing methods used in medical device production. Advanced understanding of Design for Manufacturability (DFM), process...
and emerging requirements and quality trends as they relate to medical device products worldwide. Facilitate group meetings..., technical and/or quality. 3+ years' working knowledge of FDA medical device regulations and ISO 13485, FDA, and EU regulations...
: Experience in the medical device industry Project management experience Experience with validation and qualification... business unit. Boston Scientific ranked #2 among medical device companies on Forbes America's Best Places to Work...
years of experience in relevant field(s) related to medical device quality systems and/or production and process control... or equivalent. Understanding of medical device regulations and standards applicable to the BSC Global Quality System and Process...
, design verification and design validation studies. Working knowledge of Quality Assurance in a medical device manufacturing... medical device experience preferred. Knowledge of Quality System Regulations. COMPETENCIES: Analytical Skills (e.g...