Role Description
We are seeking a dedicated professional to oversee Disposition activities within our Quality organization at our Singapore Manufacturing facility. This includes incoming and product disposition, managing post-disposition issues, and leading Quality Assurance initiatives.
Responsibilities
- Perform comprehensive Quality review to support lot disposition (approval or rejection) of raw materials, components, and products for assigned areas.
- Participate as Disposition SME review for site and network change controls.
- Act as the site Subject Matter Expert (SME) for the Disposition process within the global disposition network.
- Serve as SME for SAP ERP Quality Transactions.
- Support routine GMP documentation and review activities (e.g., SOPs, logbooks, work orders, batch production reports, electronic batch records, and validation protocols).
- Participate in and manage deviations and root cause investigations.
- Author and maintain inspection playbooks and drive inspection readiness efforts.
- Participate in regulatory inspections/audits and interact directly with regulatory inspectors/auditors.
- Lead and support site/network driven QA/OE continuous improvement initiatives.
- Manage quality performance metrics for disposition.
- Escalate significant quality, compliance, supply, and safety issues to Quality management in a timely manner.
Basic Qualifications
- Master’s degree in Biological Sciences, Chemistry, or a related technological field OR
- Bachelor’s degree in Biological Sciences, Chemistry, or a related technological field and 2 years of directly related experience OR
- Associate’s degree in Biological Sciences, Chemistry, or a related technological field and 6 years of directly related experience OR
- High school diploma/GED in Biological Sciences, Chemistry, or a related technological field and 8 years of directly related experience.
Preferred Qualifications
- Good communication skills (technical writing and verbal communication/presentation).
- Demonstrated related work experience (manufacturing, process development, or quality assurance) in the pharmaceutical industry with progressively increasing responsibility and demonstrated experience in project management, quality assurance, and quality systems.
- Ability to interact effectively with a variety of communication and working styles and work well in teams.
- Ability to manage multiple simultaneous activities in a rapidly changing environment.
- Ability to work independently with minimal supervision.
- Ability to build strong and collaborative partnerships with client groups and influence changes in practices to ensure compliant manufacturing.
Interested candidates may apply through the application system. We regret to inform only Shortlisted candidates will be notified.
EA License No. 01C4394 • RCB No. 200007268E •Derrick Tiew Yong Han EA Registration No. R1877971
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