Validation Engineer

Description Join to apply for the Validation Engineer role at PSC Biotech Corporation . Responsibilities include: Process RQs (SIP, Bulk Sterilization, Autoclave)Warehouse mapping Filtration skids Trending of Results Develop, review, and approve validation lifecycle documents, protocols, and reports in accordance with policies, standards, procedures, and...

About the RoleWe are looking for an experienced Validation Engineer to support the Commissioning, Qualification, and Validation (CQV) activities for an ongoing fill-finish expansion project. This mid-level role will involve executing qualification protocols, supporting commissioning activities, and ensuring all systems (utility and process equipment) meet...

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small,...

About No deviationAt No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful...

Introduction We at Traque are on an exciting journey of growth and are looking for a dynamic Validation Engineers to help us achieve our vision to become "your first-choice industrial solution provider". Traque provides comprehensive consulting and engineering solutions, working with multinational pharmaceutical clients to R&D facilities - across all...

Responsibilities:Hands-on experience and understanding of automated systems supporting manufacturing, IT infrastructure, Engineering and operations.Strong understanding and applicable regulations (FDA/EU/ICH), with emphasis in 21 CFR Part 11, 210, 211, and 820 and local regulatory expectations.Promoting GMP awareness and a culture of continuous improvement...

This role is responsible for supporting validation activities including develop, support and implementation. In this role, the engineer must ensure qualification activities are performed in accordance with the company’s policies and procedures, and regulatory requirements **Responsibilities**: - Support equipment, facilities, utilities qualifications, -...

Si Validation Engineer : Programming language – C & Python Good Understanding of SOC architectures and validation of Integrated IP's Test plan development and test content writing based on design specifications, architecture document & end use case scenarios for SOC's Silicon bring up, initial power-on, bootup & functional testing Preferred Memory & PCIE...

**Key responsibilities: - Perform Equipment Validation Maintenance Quality Systems review and re-qualification activities to ensure GMP equipment is continuously maintained in a validated state. Schedule own tasks to be performed as well as tasks for other Specialists as determined by the Validation Manager - Perform change control assessments for GMP...

Responsibilities: - Responsible for executing and closing out the validation activities within the assigned area. - Develop or support the development of required validation documents, including Risk Assessments, plans, protocols, and reports. - Support the review, analyse, interpret and summarise data of executed studies. - Investigate or support the...