Manufacturing Engineer

About This Role

A Production Manufacturing Operations Manager role for a GSK manufacturing site in Jurong, Singapore, requiring 2 years of experience with Clinical Good Manufacturing Practices (cGMP) and compliance roles.

Responsibilities

• Support the organization in increased alignment with GSK Quality and manufacturing system requirements for pharmaceutical, OTC, and medical device manufacture.
• Support compliance efforts including training, CAPA's, root cause analysis, non-conformance reports, audits, calibration verification, SOPs, and quality checks.
• Lead key activities to progress the scope and effectiveness of site operational programs in a global manufacturing environment.
• Assess individual and team performance, conduct audits, and ensure adherence to GSK Quality and manufacturing system requirements.
• Support the organization in increased alignment with GSK Quality and manufacturing system requirements for the manufacture of Pharmaceutical drugs, Over the Counter (OTC) drugs, and Medical Devices.
• Support compliance efforts across various areas including training, corrective & preventive actions (CAPA's), root cause analysis, non-conformance reports, audits, calibration verification, standard operating procedures,

Requirements

• Bachelor's degree or equivalent experience in Clinical Good Manufacturing Practices (cGMP) environment.
• Experience in a Compliance role.