Job Summary
A biotechnology company is in need of a Remote Senior Research and Development Good Pharmacovigilance Practice Quality and Compliance Manager.
Individual must be able to fulfill the following responsibilities:
- Provide input into the GVP/GxP annual audit strategy
- Oversee the planning, conduct, approval, and close-out of audits
- Oversee the execution of the end-to-end audit processes
Applicants must meet the following qualifications:
- Bachelor’s Degree within life sciences
- Experience in: audits, inspection management, inspection readiness, quality risk management or related
- 5+ years, GVP and/or QA or Compliance experience
- Working knowledge and solid understanding of the GxP drug development regulations
