Clinical - QA Associate, Clinical Studies

This is an on-site contract opportunity. 3 months with potential extension Under general supervision, performs work that is varied and that may be somewhat difficult in character, but usually involves limited responsibility.

Follows established protocols and work plans.

May be assisted by QA Specialists and Sr.

Specialists.

Comply with divisional and site Environmental Health and Safety requirements.

II.  Essential Functions:

• • Responsible for inspection of incoming materials for GMP production • Assist with packaging floor activities for primary and secondary (equipment/room approval, facility compliance, auditing, label inspection, line clearance, etc.)  • Reviews production batch records, logbooks and other associated documents • Performs Quality verification of just-in-time labeling activities • Performs document issuance, scanning, filing and archival activities •...