Senior QA Specialist: CGMP Data

Il y a 2 jours

NouvelleCalédonie, Nouvelle-Calédonie, France KBI Biopharma, Inc. Temps plein 107 000 € - 161 000 € Contrat

KBI Biopharma, Inc. in the United States is seeking a Senior QA Compliance Reviewer to ensure GMP data integrity in biopharmaceutical development. You will review release, in-process, and stability data, and approve method qualifications and validations, deviations, and related investigations.

The role requires extensive CGMP knowledge, experience with USP/EU/JP guidelines, and strong ability to interpret regulatory requirements and write clear reports for management.