Established company in Cincinnati, OH is looking for a Junior Validation Engineer. Qualified candidates will possess the following: Qualifications: -BS in Engineering -3-7 years experience in pharmaceuticals or medical device -Experience validating PLCs Requirements: -PLC Validation -Delta V, Allen Bradley, Siemens -CSV (Computer System Validation) -IQ/OQ/PQ -GAMP -21 CFR Parts 11, 210, 211 -CIP/SIP is a plus -RS Batch is a plus Qualified candidates please apply for immediate consideration. Required Skills
Kaplan Compliance Solutions (KCS)|Indianapolis, IN, 46278|1-2
Description As an Associate Software Quality Assurance Engineer you will Report to the Development...business process outsourcing BPO company based in Indianapolis Park 100 area...Job Location Indianapolis IN Job Number 9004BR Company URL http...
Hybrid Test Engineer Job description - Designing, developing, supporting, upgrading and supporting the procurement automatic product test equipment for new and existing products and components. - Developing documentation for test systems including schematics, calibration procedures, hardware design document, software requirements specifications, trouble shooting guidelines, and operator job instruction sheets as required. - Coordinating the creation of material
The primary purpose of this position is to manage engineering functions. Identify and evaluate procedures and process equipment required to produce a quality product. Identifies and evaluates procedures to ensure the production of quality product. Develops new and unique approaches to complex problems and can advance technology beyond previous achieved levels. Applies engineering concepts to resolve acute or chronic problems. Conducts studies to understand capability for process and/or measurement systems
Kaplan Compliance Solutions|Indianapolis, IN, 46278|>1
As an Associate Software Quality Assurance Engineer you will Report to the Development...business process outsourcing BPO company based in Indianapolis Park 100 area...As an Associate Software...and apply best practices in Software Quality Assurance using Mercury Quality Center Use and...
Responsibilities The three primary roles of this position include: feasibility testing to support the product development of medical devices; design verification testing to support device regulatory approval; and post-market device evaluation to support clinical and/or marketing activities. This position requires a technically sound engineer capable of challenging medical devices through accelerated fatigue, corrosion, electrosurgical, simulative use, and basic mechanical properties medical device testing
As an Associate Software Quality Assurance Engineer you will Report to the Development...business process outsourcing BPO company based in Indianapolis Park 100 area...As an Associate Software...and apply best practices in Software Quality Assurance using Mercury Quality Center Use and...