Job Description

Location: SingaporeStart Date: ASAPContract: 12 months contract likely to be extendedThe CompanyA service provider leading the Pharmaceutical and Medical Device sectors since 1998. A Company that is constantly growing and has over 2000 employees worldwide.Roles and responsibilitiesYou will be expected to provide support in site process engineering, installation verification, pre-commissioning, SAT and commissioning of equipment/utilities/ancillaries, used in biotech facilities.\xc2\xb7 Follow standard operating procedures and standards in a highly regulatedenvironment\xc2\xb7 Generate and execute procedures/protocols through GMP verification process\xc2\xb7 Adhere to safe work practices\xc2\xb7 Clearly communicate progress and issues to management and peers and finalizereport writing for test protocols\xc2\xb7 Perform all tasks in strict compliance with operating procedures, best practices, andregulatory requirements\xc2\xb7 Accountable for accurately completing GMP documentationCandidate Requirements\xc2\xb7 Chemical Engineering master degree\xc2\xb7 At least 3 years related process engineering design experience, with preferredexperience in biotech, with understanding of automated process equipment, systemsarchitecture and operations, and related components\xc2\xb7 Knowledge of cGMPs and main pharmaceutical standards and rules\xc2\xb7 Knowledge of process control and P&IDs standard settings and ISA standard symbology\xc2\xb7 Knowledge of safety current rules for equipment/ plants design and attention to healthand safety practices within the working environment\xc2\xb7 Previous experience in equipment and process and equipment validation is helpful, butnot just focusing on this\xc2\xb7 Technical expertise in GMP biotech processes that include upstream & downstreammanufacturing and clean utilities

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