Azzur Group is a GxP compliance and consulting organization focused on providing quality-driven solutions that propel life science companies toward success. If you're a dedicated professional with a desire to engage, learn, and adapt within a dynamic healthcare landscape, you will fit right into our core values: Put Others First, Have the Courage to Take Action, Take Personal Responsibility, and Have Fun!

Hands-on experience with mRNA starting materials from a quality/CMC perspective, particularly those used in the production of drug substances. Knowledge of the raw materials used in the production of mRNA and their applications, with a specific focus on materials supplied to clients. Ensure appropriate validation systems, supplier qualifications, and ISO certifications are in place, tailored to the manufacturing needs but not necessarily fully GMP compliant. Assist in audits and ensure compliance with required quality standards and certifications without full GMP compliance. Provide guidance on setting up and maintaining a quality system fit for the purpose of mRNA production.

This is an hourly role