Responsibilities: Ensure compliance to QA principles in manufacturing activities. Support and provide on-site appropriate QA guidance to personnel. Writing and reviewing operational documents (SOPs, Deviations, specifications, etc.) Writing and reviewing operation change control Train manufacturing employees of procedures, work instructions etc. Writing of root cause analysis investigations and execution of CAPAs Reviewing products batch records Reviewing and approving calibration reports Requirements: 2- 3 years QA experience in a Biotech company Good verbal and written communication skills Organized, detailed and accountable Proficiency in English (writing & speaking). Great inter-personal skills Please send your CV to the following: hrbio2019@gmail.com