in Engineering. 2-5 years of experience minimum. Experience in medical device manufacturing is required. Experience in process... someone with some familiarity in process validation and who is comfortable learning new equipment and executing. Requirements: BS Degree...
, more sustainable for everyone. Role Summary: In this role, you’ll be part of the team responsible for functional validation... be an individual contributor with a crucial role owning the verification and validation of vehicle electronics. You’ll work...
, more sustainable for everyone. Role Summary In this role, you’ll be part of the team responsible for functional validation... be an individual contributor with a crucial role owning the verification and validation of vehicle electronics. You’ll work...
and implement detailed validation plans tailored to specific hardware designs Collaborate with design and production teams... to understand and test against product requirements Analyze and interpret data from validation tests, offering insights...
) is a plus. Prior work experience in Medical Device Industry, Biotechnology or Pharmaceutical industry is a plus....Job Description Summary: The CSV Specialist is responsible for planning, coordinating, and executing validation...
: Bachelor's degree in engineering, Computer Science, IT, or Life Sciences. 6+ years of experience in medical device...Responsibilities: Lead and manage CSV (Computer System Validation) for GxP systems across Quality, Manufacturing...
verification, validation, and compliance test activities on electrical and mechanical medical device components/systems... requirements are met. Perform hands on test execution in the lab and at third party medical device test labs, communicate...
in a Validation or Quality Assurance role for a medical device or pharmaceutical environment. Demonstrates excellent organizational... criterion from a quantitative standpoint. The candidate must be familiar with process flow of a medical device organization...
in a Validation or Quality Assurance role for a medical device or pharmaceutical environment. Demonstrates excellent organizational... must be familiar with process flow of a medical device organization, including the regulatory impact of change and the documentation...
other duties assigned by his supervisor. Requirements: Bachelor's degree in engineering. Experience in the Medical Device... word to search medical devices manufacturing process validation, 21CFR Part 820, ISO 13485, process validation, mold...
+ years) in Computerized System Validation (CSV) within the pharmaceutical or medical device industry. Knowledge: Thorough...Job Description: Computerized Systems Validation (CSV) position involves ensuring that GxP-regulated computer systems...
(medical device or pharmaceutical preferred). Direct experience with injection molding validation, including equipment...Responsibilities: Lead validation efforts for injection molding machines, auxiliary equipment (e.g., dryers, chillers...
validation and development within the medical device, biotech, or other relevant regulated industry. Experience...Responsibilities: Author and execute Master Validation Plans (MVPs), OQ (Operational Qualification), and PQ...
, risk analysis, and manufacturing readiness. Should be experienced in Medical device manufacturing assembly lines.... Need to conduct qualification, verification, and validation activities to produce medical devices. Need to be responsible...
, you would be responsible for supporting product verification, validation, and compliance test activities on electrical and mechanical medical...Job description: As a member of the Client's Acute Therapies Verification and Validation engineering team...
assurance or software validation, preferably within the medical device industry. Strong understanding of quality standards... in medical device development. Ensure adherence to regulatory standards (FDA, ISO 13485, IEC 62304) and industry best practices...
assurance or software validation, preferably within the medical device industry. Strong understanding of quality standards... in medical device development. Ensure adherence to regulatory standards (FDA, ISO 13485, IEC 62304) and industry best practices...
, risk analysis, and manufacturing readiness. Should be experienced in medical device manufacturing assembly lines.... Need to conduct qualification, verification, and validation activities to produce medical devices. Need to be responsible...
in medical device development. Ensure adherence to regulatory standards (FDA, ISO 13485, IEC 62304) and industry best practices... in software development processes, ensuring alignment with the company's quality management system. Competencies: Medical Device...
in a regulated medical-device environment. Create URS and FMEA documentation, execute risk-based IQ/OQ/PQ/SQ, support CAPA/NCRs... engineering field. 4+ years in medical device (or similarly regulated) manufacturing. Hands-on ownership of URS, FMEA, and IQ...