We are looking for a Validation Engineer for one of our clients based out of Malaysia, it's a remote role and candidate can work from anywhere. If you are interested, Please attach your updated resume to Kalpana.Devireddy@accordinnovations.com
About the Role As a Validation Lead within Pharma TechOps, you will play a critical role in ensuring that the digital systems supporting Pharma Technical Development (PTD) meet the highest standards of quality, regulatory compliance, and patient safety. You will serve as the validation subject matter expert across a portfolio of GMP-critical systems, owning the end-to-end validation lifecycle and ensuring systems remain compliant, audit-ready, and fit for purpose throughout their lifecycle.3
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Drive high-quality strategy across products, platforms, and delivery streams.
Establish automation as the default quality approach across UI, API, integration, regression, and non-functional testing.
Drive adoption of AI-enabled quality engineering practices to improve efficiency, productivity, test coverage, and defect detection across the testing lifecycle.
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Carry out sampling and analysis of raw materials, packaging materials, in-process products, and finished products according to the approved sampling plan.
Perform investigation and basic troubleshooting for quality-related issues.
Ensure compliance with Good Laboratory Practice (GLP), Health & Safety (HSE), and quality requirements in the laboratory and workplace.
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Assist the Equipment Readiness Lead and Engineer with equipment preparation for jobs.
Perform noninvasive maintenance pertaining to the final preparation of surface and downhole equipment and ready boxes.
Execute work orders (WOs) as assigned through the Computerized Maintenance Management System (CMMS) for the Product Line, ensuring compliance to standard work as well as WO data accuracy and completeness.
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To inspect in-coming goods according to the instruction stated.
To inspect work in progress (W.I.P) by patrolling and checking the production of every machine in the designated area at least once every hour and recording this inspection on the QC hourly inspection report.
To inspect and weigh the finished goods and record such inspection by signing the inspection slip and placing this slip in the carton before taping and sealing the carton closed.
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To inspect in-coming goods according to the instruction stated.
To inspect work in progress (W.I.P) by patrolling and checking the production of every machine in the designated area at least once every hour and recording this inspection on the QC hourly inspection report.
To inspect and weigh the finished goods and record such inspection by signing the inspection slip and placing this slip in the carton before taping and sealing the carton closed.
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Support to operation sites ( WH & Copack) by validating and verifying all quality elements are adhered. Train and build competency of DC / 3rd party warehouse operations staff and transportation team related to quality i.e. traceability, GWP, aging stock management, damage stock management, stock status control, container inspection, and other assigned topics.
Manage and coordinate local trade and IMS complaints related to either ambient or temperature controlled products from distributors, retails or consumers (related to Supply Chain) or to importers with thorough investigation conducted with root causes identified and corrective/preventive actions implemented effectively.
Assess, manage and coordinate quality elements implementations in physical logistics with elements of risk assessment and followups on improvement plans. This cover all elements from supply chain after factory gate to retailers.
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Support to operation sites ( WH & Copack) by validating and verifying all quality elements are adhered. Train and build competency of DC / 3rd party warehouse operations staff and transportation team related to quality i.e. traceability, GWP, aging stock management, damage stock management, stock status control, container inspection, and other assigned topics.
Manage and coordinate local trade and IMS complaints related to either ambient or temperature controlled products from distributors, retails or consumers (related to Supply Chain) or to importers with thorough investigation conducted with root causes identified and corrective/preventive actions implemented effectively.
Assess, manage and coordinate quality elements implementations in physical logistics with elements of risk assessment and followups on improvement plans. This cover all elements from supply chain after factory gate to retailers.
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