Offer summary
Qualifications:
University degree in chemistry or biochemistry, Experience with laboratory work and HPLC systems, Knowledge of quality testing methods, Excellent proficiency in English and Lithuanian, Computer literacy, especially in MS Office.
Key responsabilities:
- Prepare and update quality control documentation based on ISO 13485
- Conduct timely quality checks of products manufactured under GMP requirements
- Ensure proper documentation is maintained and analysis results transmitted
- Coordinate product stability studies and prepare reports
- Substitute for senior quality control specialists during absences