Cqv / Validation Engineer

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 clients.We...

Roles & ResponsibilitiesThe OpportunityEsco Lifesciences Group, is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 20 countries across North America, Europe and Asia.Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first introduced in 2017.At Esco Aster Pte Ltd, we...

Roles & ResponsibilitiesThe OpportunityEsco Lifesciences Group, is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 20 countries across North America, Europe and Asia.Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first introduced in 2017.At Esco Aster Pte Ltd, we...

Roles & ResponsibilitiesPharmEng 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...

Senior CQV Project ManagerBiotechnology ManufacturingCompany: PES InternationalLocation: Portsmouth, New HampshireCompensation: Commensurate with ExperienceAbout this opportunity:PES International is an international industry leader in providing automation, commissioning, qualification, and CSV services. We have an unrivaled knowledge based in these...

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: Responsible for planning, executing and closing out the validation activities within the assigned area. Develop required validation documents, including Risk Assessments, plans, protocols, and reports. Review, analyse, interpret and summarise data of executed studies. Investigate or support the investigating of deviations or nonconformities...

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...

Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on one or more of the following areas:Process Equipment CIP / SIP Process Manufacturing and related business processes including Quality Operations and Supply Chain Operations Method validation (analytical chemistry, biochemistry,...

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...

Up to $7000 with 2 months Variable Bonus, Permanent Position:- West Singapore:- Pharmaceutical Industry Experience is a MUST:Experiences in multiple CQV discipline (such as CIP, SIP)Responsibilities: Perform riskbased commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on one or more of the following...

Senior CSV Engineer: Contract Onsite Singapore, Singapore CQV 731 SGD**Overview We have an immediate requirement for 2- CSV Specialists to join a highly skilled PM Group team based on a client site.**ResponsibilitiesDay to day activities include the following_:_**- Commissioning and Qualification of hardware and associated software to support Utility/Process...

Roles & ResponsibilitiesResponsibilities- Consults with management, assesses customer requirements, and studies product characteristics to select validation objectives and standards.- Prepares protocols for validation or performance testing of new or modified manufacturing equipment, processes, or systems.- Analyzes data from validation tests to determine...

Mission DescriptionSupporting with execution of validation strategy during and leading up to shut down period (november'24 to Jan'25) in AMSProfile Requirement Field experience with validation engineering Execution of validation, validation test, qualification test Have performed IQ and OQ and cleaning validation knowledge Worked with validation protocol...

Responsibilities: Support equipment/system qualification and cleaning validation Develop cleaning validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion Manage qualification/validation execution and lead the validation deviation investigations...

Roles & ResponsibilitiesMission DescriptionSupporting with execution of validation strategy during and leading up to shut down period (november'24 to Jan'25) in AMSProfile RequirementField experience with validation engineering Execution of validation, validation test, qualification test Have performed IQ and OQ and cleaning validation knowledge Worked with...

Roles & ResponsibilitiesValidation engineers manage, inspect, calibrate, test and modify the instrumentation, equipment, mechanics and procedures used in manufacturing. A critical aspect of their job is documenting this process so there is evidence that systems are operating safely and efficiently.Validation engineers can be found in a range of industries,...

Roles & ResponsibilitiesMission DescriptionSupporting with execution of validation strategy during and leading up to shut down period (november'24 to Jan'25) in AMSProfile Requirement Field experience with validation engineering Execution of validation, validation test, qualification test Have performed IQ and OQ and cleaning validation knowledge Worked...

About the job Serve as a site Subject Matter Expert for at least 1 specialized validation area Planning, performance, support and coordination of Computer System Validation, Equipment validation, Sterilization In Place, cleanroom validation, Clean Utilities Validation (IQ/OQ/PQ/CPV) Maintain validation status of Computer System Validation Independently...

Roles & ResponsibilitiesMain Responsibilities：1. Assist Quality and Validation Manager Asia to complete the tasks in time with good quality.2. Responsible for successful execution the Validation functions for customer project, as required – Quality, Cost, Time.3. Responsible to drive and support project team for projects where validation is required and...