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Validation Engineer

  • ... Posted on: Feb 23, 2026
  • ... PSC Biotech® Corporation
  • ... Tuas, null
  • ... Salary: Not Available
  • ... Full-time

Validation Engineer   

Job Title :

Validation Engineer

Job Type :

Full-time

Job Location :

Tuas null United States

Remote :

No

Jobcon Logo Job Description :

About PSC BiotechWho we are?PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia, and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.‘Take your Career to a New Level’PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling points which include the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure to working in Top Pharmaceutical client sites in a diverse cultural work setting.Employee Value PropositionEmployees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development through Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high-performing teams that can exceed our client’s expectations with regard to the quality of all scalable and business unit deliverables, staying under budget, and ensuring timelines for our deliverables are being met.Key Responsibilities:Review of P&IDs during commissioning phaseGeneration of Change control and System Impact Assessment (Kneat)Review vendor documents for completenessProvide SAT supportValidation document generation and protocol for equipment, including, but not limited to, process equipment and utility systems, both paper or using e-validation systems (Kneat)Execution of IQ and review/support for OQ.Closure of Change Control implementation tasksWork independently with the project manager, vendors, and contractorsProvide Quality service adhering to SOP requirementsGive necessary support for the timely completion of projectsBe present on-site to provide full-time support.Computerized systems in particular to Agilent LCMS and GCMSTemperature MappingCleanroom Qualification

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Jobcon Logo Position Details

Posted:

Feb 23, 2026

Reference Number:

28140_4369425243

Employment:

Full-time

Salary:

Not Available

City:

Tuas

Job Origin:

APPCAST_CPC

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About PSC BiotechWho we are?PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia, and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.‘Take your Career to a New Level’PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling points which include the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure to working in Top Pharmaceutical client sites in a diverse cultural work setting.Employee Value PropositionEmployees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development through Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high-performing teams that can exceed our client’s expectations with regard to the quality of all scalable and business unit deliverables, staying under budget, and ensuring timelines for our deliverables are being met.Key Responsibilities:Review of P&IDs during commissioning phaseGeneration of Change control and System Impact Assessment (Kneat)Review vendor documents for completenessProvide SAT supportValidation document generation and protocol for equipment, including, but not limited to, process equipment and utility systems, both paper or using e-validation systems (Kneat)Execution of IQ and review/support for OQ.Closure of Change Control implementation tasksWork independently with the project manager, vendors, and contractorsProvide Quality service adhering to SOP requirementsGive necessary support for the timely completion of projectsBe present on-site to provide full-time support.Computerized systems in particular to Agilent LCMS and GCMSTemperature MappingCleanroom Qualification

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