- Islandwide (Singapore) Singapore

工作地点
职位描述
岗位职责
Responsibilities:
Develop and execute validation (IQ/OQ/PQ) / study protocols as performer or witnessed by (depending on assignment) against approved URS and risk assessments.
Complete the executed test package with summary report.
Lead or support risk assessments and impact assessments where applicable.
Initiate change control process for any modifications affecting validated state.
Plan, manage and coordinate activities with other functions including equipment suppliers, Engineering, Manufacturing, QC, QA, and Automation/IT.
Track the CQV deliverables and ensure adherence to schedule from project to operation readiness.
Ensure traceability across lifecycle documents
Lead or support resolution of variation / deviation investigation in a timely and compliant manner.
Support administrative, periodic review and document revision related work.
About You:
At least bachelor’s degree or above, preferably in Engineering or Science discipline.
Candidate should have at least one year of hands-on CQV experience in the equipment qualification for example autoclave.
Working experience in supporting smoke study and / or aseptic process simulation is preferable.
Strong analytical and problem-solving skills.
Strong time management, communication and collaboration skills.
Candidate with experience in regulatory inspection by FDA / EMA will have added advantage.
Strong understanding in Data Integrity requirement (ALCOA+ principles) and Good Documentation Practice.
Duration: 6 months
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