Roles & Responsibilities: Prior JNJ TQ Experience a must Experience in validating QMS and different modules in QMS 5+years' experience with System Development Lifecyle 10+years' experience in Computer System Validation (Base...
Job Description: Performs any combination of tasks involved in the manufacture and assembly of medical devices as well as setting up, operating, performing maintenance on and troubleshooting equipment. Responsibilities: Responsible for ...
documentation Experience: Previous experience as a CSV Engineer supporting commissioning activities on lifesciences construction...
Job Summary: They are interested in temperature mapping experience, specifically CTUs, stability chambers, or similar environments. Strong lab instrument experience. 5+years of hands-on CSV in GxP environments. Experience with ris...
experience with Unix and Windows operating systems Understanding of the software development life cycle Understanding of FDA...
environments Bachelor's degree in Engineering, LifeSciences, or a related field required 5-7 years of experience in validation...
Job Summary: The Mechanical Project Development Engineer is responsible for designing and developing complex medical device components by translating engineering requirements into high-quality, compliant design solutions with limited supe...
Responsibilities: Creates Computer System Validation (CSV) deliverables (Validation Plan, Requirements Specifications, Protocols, Summary Reports, Trace Matrices, SOPs, Risk assessments). Collaborates with Business Users, System Owner, G...
Engineering, or LifeSciences. 7 to 10 years of experience as a Quality or Design Quality Engineer in the medical device industry...
Responsibilities: Lead the data quality evaluation by investigating all clinical and operational data, evaluating trends, deviations, using visual analytics tools and ad hoc reports. Manage high complex studies and support specific activ...