QC CSV Validation Engineer

We are seeking a Computer System Validation (CSV) Engineer with around 5 years of relevant experience to support QC and laboratory operations in a regulated GMP environment. The role involves ensuring that computerized systems and laboratory equipment are validated, maintained, and compliant with regulatory standards, while supporting continuous improvement...

About No deviation At 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...

As a Consultant, you will be working for our client in the respect of the applicable regulations and quality procedures and could be required to: Main Responsabilities: - Be responsible for preparing and executing test documentation for computerized systems. You should have excellent understanding of 21 CFR Part 11, 21 CFR Part 820, ISO 13485, and GAMP 5...

Roles & ResponsibilitiesResponsibilities:Work with a cross functional team in providing Quality oversight in computerized system life cycle procedure and ensure compliance to GXP standards and company policies and procedures. As the Subject Matter Expert (SME) in CSV topics, provide guidance and support to establish systems for ensuring Data integrity,...

**Position: CSV Engineer** At Coalesce Management Consulting, we are a community of people with a strong passion for excellence. We deliver bespoke project solutions within the Life Science and Technology sectors through our community of high-calibre industry specialists. We are currently expanding our team within our Life Sciences Division team and are...

As a CSV Consultant, you will be working for our clients in the respect of the applicable regulations and quality procedures. The main assignments will be: Main assignments: - To be responsible for preparing and/or executing validation activities and documentation for Computerized Systems, under respected regulations or guidelines: 21 CFR Part 11, 21 CFR...

Roles & ResponsibilitiesResponsibilities:Manage Computer System Validation Lifecycle from design to execution phases, Including relevant CSV documentations such as Configuration specification, design review, commissioning documents, and protocols. Work with QA and stakeholders to develop the CSV strategy Responsible for providing CSV documents and...

**Responsibilities**: - Commissioning and Qualification of hardware and associated software to support Utility/Process equipment. This includes Automation, PLC & SCADA plus interfaces with networks. - Documentation preparation of Commissioning, Qualification and Verification protocols (CQV) for process equipment CSV. - Field execution of Commissioning,...

**Responsibilities**: - Lead and execute Computerized Systems Validation (CSV) activities, including planning, testing, documentation, and reporting. - Collaborate closely with the Compliance Engineering team to support commissioning, qualification, and validation (CQV) activities. - Prepare, review, and approve qualification documentation (URS, DQ, FAT,...

No Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services. We strongly uphold our core...