Development Center Analyst - Pharma

Routine Analytical Activities
- Technical expertise and comprehensive understanding in method development, validation and transfer from raw materials to finished- good for new project. Conduct plan and execute the stability study until end of expected shelf- life.
- Mainly responsible for analytical technical parts, including: test method specification, project risk analysis…, coordination with third parties/vendors for the flawless execution of projects, report and escalation to project team as needed.
- Cooperate with project team to provide/plan the appropriate timeline for testing plan, obtain proper resource allocation and mitigation plans for problems during the project lifecycle to ensure that most of projects will be delivered on- time, within scope and within budget.
- Prove his/her strive for result when participating in troubleshooting, investigation.
Other laboratory activities
- Respect and apply all the requirements related to GLP.
- Participate to the routine activities of the laboratories: reference standard management, management list and document, calibration of analytical equipment, machine trouble shooting….

Good knowledge of GLP and safety in chemical laboratory, good sense of international quality guidelines (WHO- GMP, ICH guidance...) and local drug regulations.
Bachelor of Chemistry or Pharmacist. The Master of Science is a plus.
Good at using HPLC, UV spectrometer, and other instrumental analytical methods.
Proficient skills for Microsoft Word, Excel and Powerpoint.
At least 2 years background in analytical technique, especially in the pharmaceutical industry.

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Cập nhật gần nhất lúc: 2026-03-15 00:40:02