We are seeking a highly skilled and motivated engineer who is passionate about

• Project controller and executor that ensuring the projects is meet the timeline.
• Participate in developing the protocol and the report of method validation, verification, and transfer activities.
• Conduct testing using analytical instruments such as HPLC, AAS, GC, UV-Vis spectrophotometer, and dissolution apparatus related to the project.
• Prepare and review analytical reports and documentation in compliance with GMP and regulatory requirements.
• Ensure laboratory activities comply with SOPs, GLP, and GMP standards.
• Handle out-of-specification (OOS) investigations and deviation reports.
• Maintain laboratory instruments, calibration, and documentation.
• Support internal and external audits.

• Bachelor’s degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or related field.
• Minimum 3 years of experience in quality control.
• Knowledge of GMP, GLP, and regulatory guidelines.
• Experience handling (operation and troubleshooting) of HPLC, GC, AAS and other analytical instruments is preferred.
• Experience involving in a project such research and development, analytical method development and product development.
• Strong analytical, documentation, and problem-solving skills.
• Willing to work in shift and in the holiday (if needed).
• Good understanding with English both verbal and written