Johnson & Johnson Innovative Medicine in Latina, Italy, is seeking a Technical Regulatory Associate to join the Quality Systems team. You will ensure product compliance with GMP and manage local and international Change Control activities.
You will prepare registration documentation with CMC Regulatory Affairs, liaise with Janssen affiliates and authorities, and maintain regulatory master data in SAP. The role requires a master's degree in pharmaceutical sciences, 1–3 years QA experience, strong
📌 Quality Assurance Specialist and Regulatory Affairs (Italia)
🏢 Johnson & Johnson Innovative Medicine
📍 Italia
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