Pharma C&q Engineer

Key Responsibilities:Abide by all safety requirements and procedures pertaining to their role; serve as a positive model to others in this regard; re-enforce in meetings, perform periodic field observation and feedback as needed.Lead a team as the system owner in preparing and executing Biopharmaceutical Process Equipment C&Q documents, ensuring achievement...

Key Responsibilities:Develop and maintain detailed C&Q schedules using project planning tools (e.g., MS Project), aligned with overall project timelines.Collaborate with engineering, validation, QA, QC, and operations teams to plan and sequence commissioning and qualification activities.Monitor progress, identify schedule risks, and implement mitigation...

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...

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 the US, our core focus is on consistently delivering high quality outcomes for our multinational...

**Responsibilities**: - Develop and execute periodic requalification plan, IQ and OQ protocols - Coordination of maintenance and calibration activities; execute work orders and troubleshooting for maintenance and calibration till completion and release - Perform periodic review evaluation to ensure equipment and systems required for GMP operation are...

More than 380! That’s the number of associates in our Singapore Large Molecules division to support the making of medicines for our patients worldwide.**Key Responsibilities** - Planning, executing and reporting on Commissioning & Qualification for CAPEX projects - Planning, performing and reporting routine manufacturing operation ensuring GxP compliance...

Support C&Q execution for process equipment, utilities, and manufacturing systems. - Review and execute qualification protocols (IQ, OQ, PQ) and support FAT/SAT activities. - Provide process and operational input during commissioning and troubleshooting. - Support DeltaV-related activities (recipes, phases, batch execution understanding). - Develop/review...

Our client is a leading quant and systematic hedge fund, leveraging their deep knowledge of trading, technology and operations to deliver high-quality, uncorrelated returns. Seeking a C++ Developer to join their Singapore team with a background in building highly performant, resilient trading systems. As part of the Risk Technology team, your main focus...

Job Scope - Performing technical assessment and sizing for safety relief valves, rupture discs, vent devices and others. - Originating and checking PRD sizing calculations for Pressure Relief Valves, Bursting/Rupture Discs and Conservation & Breather Vents as per International Standards in API. - Specification for purchasing PRDs - Drafting Pressure Relief...

Job Scope Contribute to Life Science projects for Antaes Asia clients Develop and maintain detailed C&Q schedules using project planning tools (e.g., MS Project), aligned with overall project timelines. Collaborate with engineering, validation, QA, QC, and operations teams to plan and sequence commissioning and qualification activities. Monitor progress,...