-planing and structuring the quality assurance documentation
-getting informed and trained regarding regulations
-writing and updating the QA documentation according to international regulations
-recording and sharing QA documents
-ensuring that procedures are enforced
-ensuring that staff is trained
-monitoring deviations/action plans and modifications
-implementing and gathering data from indicators;writing,implementing and monitoring action plans in case of deviation on the field
-ensuring trace ability within the manufacturing unit
-helping to prepare the management review
-carrying out internal audits
-creating ,following up and reviewing batch records
-coordinating validation and qualification actions
-acting as quality liaison for suppliers and instructing parties.
Requirements
-Master degree(or equivalent 4-5 years university degree)or medical engineer, bachelor of biology, microbiology, pharmacy, biochemistry, chemistry, with 2 years work or internship experience
-good command of English
-knowledge of quality standards:ISO 9001 and ISO 13485 would be an asset.
WORK PLACE:
Payam- economic zone-Mehrshahr-Karaj
