Location: Cambridge,MA, USA
Schedule: Hybrid schedule with one day per week on-site in Cambridge, MA
Description:
Represent BioMedical Research Quality as eCompliance SME by educating applicable project validation team on expectations associated with validation strategy and deliverables.
Required skills:
CSV SME with experience in computer system validation of Laboratory analytical software / equipment systems as well as Lab IT systems.
Candidate must have relevant education and experience to independently perform QA validation roles according to company procedures and industry GxP best practices. Ideal candidate also has experience in GCP/GLP laboratories.
Must have strong communication, time management and effective writing skills