Salary: up to $6000
Duration: 3 months
Working Days & Hours: Mon-Fri Office Hours
Location: Kranji
Job Description
Develop and maintain detailed C&Q schedules using project planning tools (e.g., MS Project), aligned with overall project timelines.
Collaborate with engineering, validation, QA, QC, and operations teams to plan and sequence commissioning and qualification activities.
Monitor progress, identify schedule risks, and implement mitigation strategies to ensure timely delivery of C&Q milestones.
Support the development and execution of C&Q strategies, including URS, DQ, IQ, OQ, and PQ documentation and activities.
Ensure C&Q activities comply with GMP, FDA, EMA, and other applicable regulatory standards.
Facilitate planning meetings, progress reviews, and reporting to project stakeholders.
Coordinate resource planning and availability for C&Q tasks, including vendor and contractor support.
Maintain accurate documentation and change control records related to C&Q scope.
Support audits and inspections by providing schedule-related documentation and insights.
Job Requirements
Min Degree in Engineering or similar w min 3 yrs of relevant experience working in pharma manufacturing or engineering projects with
GMP
compliance.
Familiarity with validation documentation
like URS, DQ, IQ, OQ, PQ.
Interested candidates, please submit your resume to:
Ally Audrey Lok Xin Woon
Recruit Express Pte Ltd (Healthcare & Lifescience)
Company EA Licence number : 99C4599
Personnel EA License: R
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