QA Specialist - Chemistry and Manufacturing Doc Review

I have an exciting opportunity in the San Diego area for a Documentation Specialist within the Manufacturing and Chemistry department.

Position:This position is responsible for reviewing and approving device production documentation to ensure compliance with QSR and ISO 13485 requirements; the individual must maintain a high level attention to detail. Building relationships and working well with different departments and all position levels is critical. The role holder will be able to learn product lines and types quickly and efficiently to deliver results quickly. This is a temporary position. Qualifications:- Assist in resolving production batch record backlog. - Work with operations personnel to resolve good documentation practice issues with production records.- The job holder will have experience in compliance with FDA regulations and ISO 13485 standards. -- The job holder will have experience in a regulated environment. The job holder will be required to interface with various operations groups. The job holder must have thorough knowledge of Good Documentation Practice requirements- Will be required to physically move between various buildings as for document review, confirmation, and labeling. This includes manufacturing areas which require proper gowning and lab safety, warehouses which may require walking in the warehouse where chemicals and biologics are stored. If you are interested in this opportuntiy please send your resume ASAP for an interview.
To find out more about Real please visit www.realstaffing.com