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A leading pharmaceutical company in Singapore is seeking a Quality Assurance professional to review batch records, support documentation practices, and ensure regulatory compliance in a manufacturing environment. Candidates should hold a Bachelor's degree in Pharmaceutical, Engineering, or related field. This role requires active participation in audits and investigations of deviations.
Review and approve batch records, standard operating procedures (SOPs), and deviations related to manufacturing operation.
Support timely documentation and ensure adherence to GDP (Good Documentation Practices).
Participate in internal audits and support regulatory inspection.
Provide on-the-floor QA presence to oversee manufacturing activities and ensure compliance with GMP.
Assist in the investigation of deviations, non-conformances, and complaints.
Bachelors degree in Pharmaceutical, Engineering or related field.
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