About this role
QA GMP associate at Alsglobal. Location: Sophia-Antipolis, Provence-Alpes-Côte d'Azur, France. Role: reviewing documents, conducting audits, supporting operations Requirements: Associates in biotechnology (BAC+2) and minimum 3 years production experience with biotech medicines; QA/GMP, document review, internal auditing, SOP maintenance, microbiology support, validation and KPI reporting. Category: Research and Development (R&D) Seniority: Mid Level Commitment: Full Time Workplace: Onsite Languages: French