
Software & Validation Quality Engineer 1
- Woodlands, Singapore
- Permanent
- Full-time
- Provide quality support to new and sustaining verification/validation activities focusing on System, Software, Test Method, MES modeling, Process and/or Facilities & Utilities in Manufacturing area of in charge.
- Provide quality support to Development, Lifecycle Management and Manufacturing functions for verification & validation planning and transfer activities. Assist teams in determining verification and validation needs and requirements.
- Provide quality support for automated system/software development projects in the manufacturing areas by reviewing and approval of system/software deliverables, in accordance to Illumina Procedures and Work Instructions.
- Provide quality assurance support to validation related NCR and CAPAs.
- Participate in the development and implementation of validation quality initiatives to address process and system inadequacies to achieve continual quality improvement objectives.
- Support in the review and approval of Manufacturing system/software/process and/or facilities related change requests.
- Support in the transfer of system/software/process from development into manufacturing product support.
- Ensure compliance of validation efforts performed by internal/external validation personnel.
- Ensure validation quality activities are in alignment with company goals, objectives and in compliance with Quality Systems.
- Participates and provides support in customer, regulatory, internal and corporate audits.
- Responsible for escalating potential risks to Management.
- Responsible for exhibiting professional behavior with both internal/external business associates that reflect positively on the company and is consistent with the company’s policies and practices.
- Provide support in the implementation plans for adherence to new regulatory requirements or expectations.
- Perform other duties as may be assigned by Management.
- Bachelor’s degree; or equivalent experience in Computer Science, Software Engineering, Informatics, Biological/Life Sciences.
- 0-2 years of Validation Quality and Software Quality Engineering or relevant experience in a regulated environment, in vitro diagnostics/medical device.
- Basic understanding of the applicable regulations and standards: 21CFR 820, 21CFR Part 11, ISO 13485, IEC62304, ISO14971, GAMP5.
- Basic knowledge of System/Software Development Lifecycle Models, Software Verification & Validation, Software Configuration Management (SCM), Process Validation, Test Method Validation, Facilities Validation and Risk Management Process.
- Basic knowledge on statistics, sampling plans, and statistical analysis.
- Experience with Microsoft Office, including Word, Excel and PowerPoint.
- Excellent attention to detail, strong organization skills, and ability to work independently and in teams.
- Excellent interpersonal skills.
- Excellent communication skills, critical thinking and problem-solving abilities.
- Ability to operate flexibly in fast-paced environment.
- Ability to deliver quality outputs under minimal supervision and guidance.
- Ability to influence decision at critical points in time during system/software development lifecycle.