Our client needs a Validation Technical Writer with at least 8-10 years’ experience in a Pharmaceutical or Biotech field. This contractor will be responsible for creating, authoring, and reviewing and pushing through a backlog of 70 Validation Documents. This person will also be working cross functionally with stakeholders and other departments heads; QA, Engineering. The candidate will be working through the EDMS system Veeva.
Validation Documents, Protocols, Early Phase GMP Regulations, Veeva
Working with a company that has had to make a facility GMP Compliance for Early Phase I Clinical Trials.
Remote: Validation Technical Writer (232395)