QA Document Control

Job Responsibilities

1. Responsible for the preparation of document codes and the establishment and updating of document directories;
2. Responsible for the review, printing, circulation, signing, stamping, issuance, archiving, re-evaluation, retrieval, destruction, and management and control of all GMP document formats, fonts, and layouts. Keep appropriate records of the distribution, retrieval, destruction, and archiving of documents and perform a pre-archiving review of document format, font, layout, and content completeness.
3. Determine the departments for review of GMP documents according to document requirements, and be responsible for the storage, organization, and monitoring of the retention period of documents.
4. Responsible for the periodic review of documents from various departments and timely notification of periodic revisions.
5. Responsible for the collection, photocopying, binding, distribution, retrieval, and archiving of auxiliary records from various departments.
6. Ensure that the documents currently in use are the approved current versions to prevent the misuse of outdated documents.
7. Archive inspection and cooperation for internal/external audit documents.
8. Responsible for the training of related documents within your scope of responsibility. Coordinate with other system document and training administrators to ensure that every effective document has been adequately trained.

Job Requirements

1. Major in Biology, Chemistry or related fields, with at least a college degree;
2. Possess strong team spirit, coordination skills, and communication abilities;
3. Proficient in using computers and able to appropriately edit documents according to SOP requirements.

HR Email: hr@biotech-pack.com (If interested, please contact us through this email or directly submit your resume)