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Regulatory Compliance Professional
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Equipment Qualification and Validation Professional
2 weeks ago
- To develop and execute equipment qualification and validation plans and protocols, ensuring compliance with Singapore Guideline for Good Manufacturing Practice (GMP) and other regulatory requirements.
- To conduct routine review of qualification and validation processes and documentation, identifying areas for improvement and implementing changes as needed.
- To ensure timely calibration and corrective/preventive maintenance of equipment, minimizing downtime and maximizing efficiency.
- To develop and maintain an accurate and up-to-date equipment database, including the pharmacy master equipment list, activity trackers, and equipment records and data files.
- To collaborate with internal stakeholders to schedule equipment activities, minimizing disruption to operational activities and ensuring seamless execution.
- To liaise with external stakeholders to procure and service equipment, managing relationships with vendors and service providers to ensure timely delivery and high-quality services.