as required. Assists in validation of complete system functionality and solves problems with subcontractors and other trades to ensure...
Johnson Controlsengineer - draft Validation Plans, Requirements, Test Cases, Summary Reports Manage the systems and processes for change... our collective expertise Senior CQV Engineer Responsibilities: Lead a Team through the qualification effort of making a lab...
Veristaof equipment/large upgrades/extensive product updates. Perform functions of validation engineer - draft Validation Plans...Responsibilities: Manage the validation and documentation related to complex computer systems, multiple pieces...
Katalyst Healthcares & Life Sciencesour collective expertise Senior CQV Engineer Responsibilities: Manage the validation and documentation related to complex... engineer - draft Validation Plans, Requirements, Test Cases, Summary Reports Manage the systems and processes for change...
Veristaengineer – draft Validation Plans, Requirements, Test Cases, Summary Reports Manage the systems and processes for change... expertise Senior CQV Engineer Responsibilities: Lead a Team through the qualification effort of making a lab...
Veristaexpertise Senior CQV Engineer Responsibilities: Manage the validation and documentation related to complex computer... systems, multiple pieces of equipment/large upgrades/extensive product updates Perform functions of validation engineer...
Veristaand validation documentation for standard equipment/systems/ software, and processes as part of team as directed by the project.... Maintaining clear, detailed records qualification and validation Documenting impact and risk assessments as part of a team...
Veristaexpertise Responsibilities: Authoring, editing, and executing technical commissioning, qualification and validation..., detailed records qualification and validation Documenting impact and risk assessments as part of a team. Completing user...
Veristaand your future. Your Role We are hiring an experienced Validation Engineer to join our team in Indianapolis. The... successful candidate will have a strong understanding of pharmaceutical manufacturing processes, regulatory requirements, and validation...
PSC Biotech. External applicants must be eligible to work in the US. Your Role: The Validation Engineer II is responsible for providing... support to all validation activities within the Indianapolis site. This position is responsible for compliance...
Merck GroupSenior Validation Engineer based at our USA office (Indianapolis) Job Description: The Senior Validation Engineer... will be responsible for the preparation, review, and approval of quality and validation related documentation and ensuring compliance...
PACIVto support team in compliance of validation effort Independent verification of testing against specifications Managing... and validation documentation for standard equipment/systems/ software, and processes as part of team as directed by the project...
Veristastandards to support team in compliance of validation effort Independent verification of testing against specifications..., qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed...
VeristaWorkplace Award, which recognizes the most engaged workplace cultures in the world. System Test / QA Validation Engineer... – Indianapolis, IN Allegion is seeking a dedicated and experienced System Test / QA Validation Engineer to join our team...
Allegion! As a Validation Engineer at PSC Biotech, you will play a critical role in driving project success, while supporting validation... and your future. Your Role This is an open application for Validation Engineers in the life science industry. We look...
PSC Biotech. Manage validation and documentation for complex computer systems, equipment upgrades, and product updates. Draft and execute... validation plans, requirements, test cases, and summary reports. Oversee change control processes for laboratory equipment...
Darwin Recruitmentsmall and large capital projects in a cGMP environment. Participate in the development of the following Validation efforts...: Validation Planning, Protocol Generation, Protocol Execution, Familiar with GAMP/GMP process, and not limited to FATs/SATs...
Katalyst Healthcares & Life Sciences