I have two years translation/interpretation experience in a pharmaceutical manufacturing company. I translated documents for quality systems and GMP related to drugs, medical devices, and cosmetics. I did both English to Japanese translation and Japanese to English translation.
Examples of documents I translated or proofread:
-FDA (Warning letters, regulatory information, audit letters)
-EU Medical Device Directive (regulatory information)
-ISO9001 & ISO13485 (manuals, SOPs, technical documents, audit letters)
-general business letters...