Senior CQV Engineer

**About the Role**: Join our team as a **CQV (Commissioning, Qualification & Validation) Engineer**, supporting the start-up and validation of state-of-the-art pharmaceutical/biotech manufacturing facilities. You will work closely with project, engineering, and quality teams to ensure all systems meet GMP compliance and are ready for commercial...

Due to our constant growth, we are looking for a Senior CQV Engineer with strong experience in laboratory equipment and lab decommissioning activities to support our projects in Singapore.You will be responsible for:Leading commissioning, qualification, and decommissioning activities specifically related to laboratory equipment and facilities.Preparing,...

Job DescriptionThe CQV Engineer is responsible for the commissioning, qualification, and validation of CU/Cleanroom/Temperature Controlled Unit/Process systems. The role ensures that all systems are installed, tested, and qualified in compliance with cGMP, regulatory requirements, and project-specific standards.RequirementsBachelors Degree in Engineering,...

About the Role: We invite highly motivated individuals to join our team in providing support to our clients' biomanufacturing facilities. In this role, you will be tasked with performing pre-commissioning checks and detailed testing, troubleshooting process/equipment issues, preparing comprehensive reports, collaborating with cross-functional teams, and...

**Senior CQV Project Manager** Biotechnology Manufacturing **Company**: PES International **Location**: Portsmouth, New Hampshire **Compensation**: Commensurate with Experience **About this opportunity**: PES International is an international industry leader in providing automation, commissioning, qualification, and CSV services. We have an unrivaled...

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...

PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective...

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...

**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...

Responsibilities: The incumbent will lead commissioning, qualification, and validation (CQV) activities for Lab Equipment. About You: Diploma/Degree in Engineering or Science Disciplines with at least 5 years’ experience in lab equipment CSV (computer system validation). Preferably 5 – 10 years experience in analytical instrument CSV. Knowledge towards...