Join Grifols, a global healthcare company, as a CQA Quality Control & Process Specialist. Participate in the development and review of Clinical SOPs, Regulatory documents, and Study Plans. Provide quality oversight on the conduct of clinical studies and interact with the Drug Development department to resolve compliance issues.
Requirements
- Life Sciences Degree
- A minimum of 5 years in a similar role or provide experience in Quality and Clinical Trials
- Abilit...
Requirements: 5+ years of experience in Quality and Clinical Trials, Life Sciences Degree, and advanced knowledge of ICH/GCP Guideline, EDC systems, and medical terminology