Alterity Therapeutics is seeking a remote US-based Document Control Specialist to support Regulatory Affairs and QA teams in clinical, nonclinical, and CMC areas. You will QC scientific documents, manage repositories, and prepare submission packages for audits and inspections.
The role requires a life sciences degree and experience with regulated documentation, along with strong attention to detail and MS Office proficiency.
#J-18808-LjbffrRemote Scientific Documentation Specialist for Regulatory QA in workfromhome at Unknown Company
This position is listed as full time and able to be worked remotely.