Cqv Engineer- Upstream/downstream Process Equipments

PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors. With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our multinational...

**Responsibilities**: - Assist establishment of Drug Substance process development, support and troubleshoot biologics commercial upstream / downstream manufacturing processes - Plan, design, execute and interpretation of lab experiments to support plant operations, troubleshooting, process mapping, process transfer, process improvements and/or the...

**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...

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...

**Responsibilities**: - Perform routine manufacturing processes and equipment preparation (CIP, PT, SIP, etc.) - Support day to day production activities and record data according to Electronic Batch Record (EBR) in compliance with GMP, Environmental, Health and Safety guidelines. - Perform equipment and process monitoring - Able to communicate with...

PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors. With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes for our multinational...

**Responsibilities**: - Assist establishment of Drug Substance process development, support and troubleshoot biologics commercial upstream / downstream manufacturing processes - Plan, design, execute and interpretation of lab experiments to support plant operations, troubleshooting, process mapping, process transfer, process improvements and/or the...

**Responsibilities**: 1. As the region's projects top manager, is responsible for the management and optimization all parts of project include technical, sales and market, supply chain, quality, fulfillment and so on. 2. Oversee and optimize projects related to petroleum extraction and refining equipment or parts. Responsible for technical assessments and...

Our client is seeking a CQV Engineer (Commissioning, Qualification & Validation) to join their team. Are you ready to play a crucial role in the pharmaceutical industry? Join a dynamic team as a CQV Engineer, where you\'ll support the start-up and validation of cutting-edge pharmaceutical and biotech manufacturing facilities. This opportunity offers the...

Roles & ResponsibilitiesAbout 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...