, solving complex challenges related to life sciences. We are looking for a dedicated Validation Engineer to join our talented..., qualification, validation, consulting, etc.) as developed and defined in project agreements with IPS clients. You will also follow...
lives of people, solving complex challenges related to life sciences. We are looking for a dedicated Validation Engineer... (commissioning, qualification, validation, consulting, etc.) as developed and defined in project agreements with IPS clients...
, Re-Qualification, Validation, deviation and change control process. Advance knowledge of pharmaceutical, laboratory...
our collective expertise The Quality Systems Specialist/Admin will be responsible for maintaining various quality and validation... vault (Quality, RIM, Clinical), learning management system, validation lifecycle management system, electronic signature...
expertise The Quality Systems Specialist/Admin will be responsible for maintaining various quality and validation... vault (Quality, RIM, Clinical), learning management system, validation lifecycle management system, electronic signature...
our collective expertise Lead CSV Engineer/Analyst Responsibilities: Authoring, editing, and executing technical commissioning..., qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed...
Job Title: CQV Engineer Job Description Assisting in development, review, and approval of cGMP documents including..., but not limited to: Master Validation Plans, FAT/SAT documents, Turnover Packages, SOP’s, specifications, traceability matrices...
Job Title: CQV Engineer Job Description Assisting in development, review, and approval of cGMP documents including..., but not limited to: Master Validation Plans, FAT/SAT documents, Turnover Packages, SOP’s, specifications, traceability matrices...
our collective expertise Lead CQV Engineer/Analyst Responsibilities: Authoring, editing, and executing technical commissioning..., qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed...
our collective expertise Lead CQV Engineer/Analyst Responsibilities: Authoring, editing, and executing technical commissioning..., qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed...
expertise Associate Project Engineer Responsibilities: Manage validation documentation in automated systems, including... document control and archiving. Perform quality reviews of IQ/OQ/PQ protocols, test scripts, and validation reports...
expertise Lead CQV Engineer/Analyst Responsibilities: Authoring, editing, and executing technical commissioning..., qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed...
expertise Lead CQV Engineer/Analyst Responsibilities: Authoring, editing, and executing technical commissioning..., qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed...
our collective expertise Associate Project Engineer Responsibilities: Manage validation documentation in automated systems..., including document control and archiving. Perform quality reviews of IQ/OQ/PQ protocols, test scripts, and validation reports...
expertise Lead CSV Engineer/Analyst Responsibilities: Authoring, editing, and executing technical commissioning..., qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed...
Overview: Reporting to the Senior Director, Quality Assurance & Regulatory Affairs, QMS Engineer will play key role... in managing Quality Management System; Quality Engineering functions; Internal & External audits, Validation...
facilities. We are looking for a dedicated Senior Process Automation Engineer to join our talented team at our office located in... development and participate in systems analysis, validation, and verification. Identify, qualify, and collaborate with third...
Job Summary The Quality Compliance Engineer II is responsible for maintaining the compliance of TMCs products... practices, ISO 13485, GDP, validation, and verification/qualification. Develop and maintain expertise in applicable quality...
all actions are completed before closure. Perform or participate in validation activity and keep validation records... management, validation and change controls. Working Knowledge in the following fields: ISO13485 FDA 21 CFR 820 Internal...
Engineer/Scientist acts as a technology transfer lead in the parenteral manufacturing MS&T group. This position is accountable... effective working relationships with other division groups in support of technology transfer, validation, and process support...