HPLC Scientist for the QC and Analytical Development Department.
Job Description
- The work involves analytical and chromatography methods development.
- Leading assigned tasks throughout all stages, including data analysis, interpretation, and documentation of results.
- Provide analytical support to process development departments.
- Performed analytical testing for products release; working in compliance with GMP requirements.
- Scientific writing, protocols, reports and procedures.
Requirements
- At least 5 years of experience in HPLC method development in the pharmaceutical industry, specifically focusing on proteins and peptides.
- Work experience in QC laboratory under GMP requirements.
- Master in Chemistry/ Biotechnology or related fields; Ph.D.- Advantage.
- Management experience.
- Advanced analytical and processing skills, ability to perform under intensive workload.
- A proactive, responsible, professional and thorough person.
- Ability to work accurately, a team player, excellent social skills, independent and self-motivated.
- Excellent English skills for clear communication in both reading and writing.
