-       Contribute to Life Science projects for Antaes Asia clients

-       Lead complex technical investigations into manufacturing deviations, non-conformances, and environmental excursions.

-       Utilize structured Root Cause Analysis (RCA) tools (e.g., Fishbone, 5 Whys, FMEA) to identify underlying triggers.

-       Author comprehensive investigation reports that withstand rigorous internal and external regulatory audits (FDA,EMA, etc.).

-       Perform impact assessments on product quality, safety, and efficacy.

-       Design and implement Corrective and Preventive Actions (CAPAs) to eliminate recurrence of deviations.

-       Monitor the effectiveness of implemented CAPAs through data-driven metrics.

-       Identify trends in manufacturing data to proactively suggest process improvements and "Right First Time" (RFT) initiatives.

-       Provide real-time engineering floor support to troubleshoot equipment malfunctions or process drift.

-       Collaborate with Quality Assurance(QA) and Production teams to ensure all activities align with Standard Operating Procedures (SOPs).

-       Participate in the drafting and revision of SOPs, Batch Records, and Validation protocols.

-       Contribute to the promotion of Antaes services on top of assistance provided to clients