Quality Control Analyst
ืคืืจืกื ืืชืืื ยท 0 ืืืขืืืื
ืฉืืืจื, ืืืฉื ืื ืืืืงืช ืืชืืื. ืคืชืืืช ืืฉืืื ืืื ื ืืืงืืช ืืื ืฉื ืืืช.
ืชืืืืจ ืืืฉืจื ืืืื
ืืืฉืจื ืืืงืืจืืช ยท ื ืฉืืจ ืืขืืื๐ฌ QC Analyst
A leading pharmaceutical company in the central region is seeking a QC Analyst to join its Quality Control laboratory in a professional, technologically advanced, and innovative environment.
Responsibilities
โข Perform analytical and physical testing of raw materials, packaging materials, and finished products.
โข Conduct analyses using chromatographic methods and a variety of analytical technologies.
โข Document, review, and approve test results in accordance with quality procedures and GMP requirements.
โข Write protocols, reports, work instructions, and standard operating procedures (SOPs).
โข Participate in process improvement projects, implementation of new technologies, and the advancement of professional initiatives within the laboratory.
Requirements
โข Previous experience as a QC Analyst/Technician in the pharmaceutical industry is required.
โข Experience working in a GMP environment is required.
โข At least two years of hands-on experience performing chromatographic analyses is required.
โข Bachelor's degree in Exact Sciences, Life Sciences, Chemistry, Biotechnology, or a related field is required.
โข High level of English proficiency (reading and writing) is required.
โข Immediate availability is an advantage.
๐ก This is an excellent opportunity to join a leading pharmaceutical company and become part of a highly professional Quality team, working in a cutting-edge technological environment with exposure to innovative projects and initiatives.
ืฉืืืืช ืขื ืืืฉืจื
- ืืืฉืจื ืื ืฆืืื ื ืฉืืจ. ืื ืื ื ืืฆืืืื ืฉืืจ ืจืง ืืฉืืืขืกืืง ืืคืจืกื ืืืชื.