QA Process Specialist

About the role

Johnson & Johnson is looking for a permanent QA Process Specialist to join the Quality team at its manufacturing site in Borgo San Michele, Latina, Italy. The role ensures that products and processes fully comply with national and international pharmaceutical regulations, supporting the delivery of safe and effective medicines.

Key responsibilities

• Manage complex investigations, ensuring compliance with GMP, regulatory, and company requirements.
• Act as Quality Leader for investigation approvals and define investigation strategies.
• Lead escalation processes in accordance with company procedures.
• Provide training and mentorship to new hires on investigation procedures.
• Serve as backup for Quality Oversight, executing controls, coordinating periodic meetings, and reporting trends.
• Maintain a constant presence on the shop floor to support operational areas and train personnel on new regulations.

Required profile

• Experience in pharmaceutical or medical device manufacturing environments.
• Strong knowledge of GMP and regulatory standards.
• Ability to lead investigations and drive corrective actions.
• Excellent communication skills for cross‑functional collaboration.
• Proactive attitude with a focus on continuous improvement.

Required skills

• GMP compliance
• Quality Assurance processes
• Investigation management