validation engineer

The Opportunity Esco Lifesciences Group is Singapore's most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania. Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in 2017. Esco...

Job Title: Validation Engineer Hiring Manager: Senior Manager Validation (Modulus Singapore) Location: Tuas, Singapore About The Job Mission Sanofi Manufacturing and Supply organization is preparing its future through an ambitious program named Modulus. The Modulus Project is at the cornerstone of Sanofi strategy as it aims at creating a new...

About Akkodis Akkodis, is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation. With a shared passion for technology and talent, 50,000 engineers and digital experts deliver deep cross-sector expertise in 30 countries across North America, EMEA and APAC....

Key Responsibilities: Execute commissioning, qualification, and validation (CQV) activities for GMP-regulated pharmaceutical and biopharmaceutical facilities. Prepare and review validation documentation, including Validation Plans, IQ/OQ/PQ protocols, test scripts, and final reports. Support equipment, utilities, facilities, and computerized systems...

Our esteemed client, an established MNC, is searching for a Validation Engineer: Job Responsibilities: Execute commissioning, qualification, and validation (CQV) activities for GMP-regulated pharmaceutical and biopharmaceutical facilities. Prepare and review validation documentation, including Validation Plans, IQ/OQ/PQ protocols, test scripts, and final...

RQ of Utilities (WFI) Process RQs (SIP, Bulk Sterilization, Autoclave) Cleaning validation Warehouse mapping Filtration skids Mixing tank Washer qualification Trending of Results Data mining LIMS queries Develop, review and/or approve validation lifecycle document and protocols/reports in accordance with relevant policies, standards,...

About the RoleWe are seeking a Validation Engineer to support validation and CQV activities for pharmaceutical and biopharmaceutical projects. The successful candidate will be responsible for ensuring equipment, facilities, utilities, and systems are validated in accordance with GMP requirements and regulatory standards while supporting project delivery from...

Job Summary: The incumbent will independently lead validation activities for assigned equipment, processes, and computerized systems within a pharmaceutical facility. Responsibilities:·Develop and execute validation protocols(IQ/OQ/PQ, process validation, cleaning validation) and author final reports ·Lead validation risk assessments and ensurecompliance...

Validation Engineer Location:Tuas Contract:Initial 12-month contract with potential to extend Industry:BiopharmaceuticalOrion Group Life Sciences are currently recruiting aValidation Engineeron behalf of our multinational biopharmaceutical client based in Tuas.This is an initial12-month contract with potential to extend .Key ResponsibilitiesDevelop and...

Job Description & RequirementsJob Description: Completing work assignments as specified by the Validation Project Manager Providing timely updates to the Validation Project Manager Adhering to the proper site safety practices; wearing adequate safety equipment when required Completing timesheets and expense reports in a timely manner Working in a...

About Akkodis Akkodis, is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation. With a shared passion for technology and talent, 50,000 engineers and digital experts deliver deep cross-sector expertise in 30 countries across North America, EMEA and APAC....

Key Responsibilities: Execute commissioning, qualification, and validation (CQV) activities for GMP-regulated pharmaceutical and biopharmaceutical facilities. Prepare and review validation documentation, including Validation Plans, IQ/OQ/PQ protocols, test scripts, and final reports. Support equipment, utilities, facilities, and computerized systems...

RQ of Utilities (WFI) Process RQs (SIP, Bulk Sterilization, Autoclave) Cleaning validation Warehouse mapping Filtration skids Mixing tank Washer qualification Trending of Results Data mining LIMS queries Develop, review and/or approve validation lifecycle document and protocols/reports in accordance with relevant policies, standards,...

Job Summary: The incumbent will independently lead validation activities for assigned equipment, processes, and computerized systems within a pharmaceutical facility.ResponsibilitiesDevelop and execute validation protocols(IQ/OQ/PQ, process validation, cleaning validation) and author final reportsLead validation risk assessments and ensurecompliance with...

Job Title: Validation EngineerHiring Manager: Senior Manager Validation (Modulus Singapore)Location: Tuas, SingaporeAbout the jobMissionSanofi Manufacturing and Supply organization is preparing its future through an ambitious program named Modulus. The Modulus Project is at the cornerstone of Sanofi strategy as it aims at creating a new manufacturing concept...

Validation Engineer – Cleaning Validation Location: Singapore, Tuas. Industry: Pharmaceutical Manufacturing | Life Sciences Key Responsibilities Support execution of Cleaning Validation activities for GMP manufacturing equipment and process systems.Develop, review, and execute Cleaning Validation protocols and reports.Support cleaning validation...

RQ of Utilities (WFI)​Process RQs (SIP, Bulk Sterilization, Autoclave)Cleaning validationWarehouse mappingFiltration skidsMixing tankWasher qualificationTrending of ResultsData miningLIMS queriesDevelop, review and/or approve validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and...

Roles & Responsibilities Key Responsibilities: Execute commissioning, qualification, and validation (CQV) activities for GMP-regulated pharmaceutical and biopharmaceutical facilities. Prepare and review validation documentation, including Validation Plans, IQ/OQ/PQ protocols, test scripts, and final reports. Support equipment, utilities, facilities,...

Validation Engineer - Cleaning ValidationLocation: Singapore, Tuas.Industry: Pharmaceutical Manufacturing | Life SciencesKey ResponsibilitiesSupport execution of Cleaning Validation activities for GMP manufacturing equipment and process systems.Develop, review, and execute Cleaning Validation protocols and reports.Support cleaning validation lifecycle...

Join us for the world we are making, redefining biosolutions for current and future generations to come, transcending planetary boundaries, sustainability, and One Health. GrowthWeempower each other to produce better resultsby providingprofessional advancement and personalgrowth. Weare driven by the challenge of creating something new and discovering better...