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Job Description
Job Purpose
- Responsible for computer system validation activities and any deliverables related to new and existing systems.
Key Accountabilities/Responsibilities:
- Develop/ issue & update SOPs, stating the scope, rationales and schedules for computer system validation activities.
- Lead the validation working parties for planning & coordinating the different computer system validation activities and deliverables related to new and existing systems
- Conduct and ensure all computer system validation testing required for new and existing systems are implemented according to CSV plan.
- Prepare the required validation documentation, DO reports, IQ/OQ reports, PQ protocols and reports, interim reports and validation summery reports for new systems according to the validation life cycle.
- Conduct validation review practices for scheduled systems and generate the validation review reports and follow up completion of relevant action plans
- Ensure completion of all validation work required for specific change control requests up to their final closure.
- Serve as a subject matter expert during internal/external audits.
- Adhere to company EHS/GMP policies and follow up roles. In addition, make the most use of GPS tools for effective information search and on-going improvements in way of working.
Job Requirements
Why You?
Basic qualifications:
- Bachelor degree in Engineering (Electrical Major)
- Previous experience in quality function is required at least 2 years.
- Good communication skills and Technical background.
- Very good English.
- Very good Computer skills.
Why GSK?:
At GSK, our mission is to improve the quality of human life by enabling people to do more, feel better and live longer. Our three world-leading businesses research and deliver innovative medicines, vaccines and consumer healthcare products. We need a talented and motivated workforce to deliver against our strategy. To achieve this, we strive to attract the best people and to create an environment that empowers and inspires.
