Your responsibilities will include

: - Managing quality assurance in the GMP control laboratory and overseeing the GMP-compliant release of therapeutic molecules

- Reviewing documents and data for quality and compliance and supporting validations and qualifications

- Actively contributing to the continuous improvement of processes and the quality management system

- Supporting OOS cases, deviations, CAPAs, and change control processes

• - Participating in internal, external, and supplier audits and conducting employee training.