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Job Description
- Responsible for monitoring aseptic lines (Vial & ampoule) and report any deviations
- Responsible for monitoring dispensing in warehouse and report any deviations
- Responsible for monitoring packaging lines activities and report any deviations
- Responsible for creation and monitoring of IPC requests for samples withdrawal
- Responsible for monitoring material receiving in warehouse and report any deviations
Job Requirements
- Bachelor’s degree in Chemistry, Science, or a related field.
- 1-3 years of experience in a quality assurance or analytical chemistry role within the pharmaceutical industry.
- Strong knowledge of GMP, GLP, and relevant regulatory requirements.
- Proficiency in analytical techniques such as HPLC, GC, UV-Vis spectroscopy, and titration.
- Experience with laboratory information management systems (LIMS) and electronic documentation.
- Excellent attention to detail and strong organizational skills.
- Ability to analyze and interpret complex data accurately.
- Effective communication skills for reporting and cross-functional collaboration.
- Demonstrated problem-solving abilities and a proactive approach to quality issues.
- Willingness to work onsite in a laboratory and production environment.
