Job description:

• Participate in the development and improvement of quality system documentation.
• Participate in change control and deviation management, as well as internal audits and Gemba activities.
• Conduct internal training on the process system and guidelines of the Pharmaceutical Quality System.
• Prepare, distribute, and review batch records; review analytical records and release finished product batches.

Job requirement:

• Pharmacist, Engineer, or Bachelor’s degree in related fields (Chemistry/Biology); Intermediate-level Pharmacy qualification.
• At least 2 years of experience in a QA position in a pharmaceutical manufacturing plant or equivalent roles (QC, R&D, Production).
• Knowledge of pharmaceutical law, GMP requirements, manufacturing processes, testing process, validation.
• Knowledge of Pharmaceutical Quality system (GMP-WHO, GMP-EU,…)
• Ability to read and understand technical documents in English. Basic English listening and speaking skills for work.

Please contact our Recruiter or apply via email recruitment@davipharm.info