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...

: PM Group is currently looking to expand the CQV capabilities in Singapore. We are looking for CQV Engineers who will bring their expertise with them and drive our projects to completion. : - Field execution of Commissioning, Installation & Operational Qualification (IQ/OQ), Verification for downstream process equipment, CIP, & Clean utilities -...

**About the Role**: We are hiring an experienced CQV Engineer (Clean Utilities & HVAC) to join our our team supporting our client on the execution phase of a brownfield pharmaceutical expansion in Singapore. This role will focus on hands-on execution, coordination, and closure of qualification activities to ensure readiness for operational use and regulatory...

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,...

About the RoleWe are hiring an experienced CQV Engineer (Clean Utilities & HVAC) to join our our team supporting our client on the execution phase of a brownfield pharmaceutical expansion in Singapore. This role will focus on hands-on execution, coordination, and closure of qualification activities to ensure readiness for operational use and regulatory...

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...

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...

**Essential Duties and Responsibilities: Generates and executes CQV protocols for facilities, utilities, equipment (e.g. Autoclaves, Chambers, Rooms, HVAC, etc.), and computerized systems (e.g. Delta V, HPLCs, Spectrophotometers, etc.). Performs basic data and statistical analysis (e.g. Temperature, Pressure, etc.). Generates CQV plans, traceability...

**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...