Global Head of Quality Systems & Risk Management

Recordati S.p.A; Milano; Ibrido; EUR 80.000 - 100.000; Tempo pieno

Descrizione del lavoro

Recordati S.p.A in Milano seeks Head of Quality Systems and Risk Management to lead global QMS and QRM across GMP manufacturing, laboratories, supply chain, distribution operations, contract partners and affiliates. You will act as corporate process owner for quality systems, ensuring compliance, inspection readiness, patient safety, product quality and continuous improvement across the organization.

Fluent in English; Bachelor degree in a related field and 12–15 years of pharma quality

Competenze

• Bachelor degree required in pharma, chemistry, engineering, microbiology or related field.
• Experience with QMS governance and quality systems.
• 12–15 years of progressive pharmaceutical quality experience.

Mansioni

• Govern global Quality Management System and ensure effectiveness of its quality elements.
• Drive quality metrics, analytics and system trending.
• Establish standards for APR/PQR processes.
• Lead enterprise Data Integrity strategy and oversight.
• Govern Supplier Quality requirements and performance monitoring.
• Lead inspection readiness programs and support health authority inspections.
• Establish global risk-based auditing program.
• Support acquisitions, integrations and global harmonization programs.

Conoscenze

QMS governance

Risk management

Regulatory compliance

Cross-functional leadership

Data-driven decisions

Quality culture transformation

Formazione

Bachelor degree in Pharmacy, Chemistry, Engineering, Microbiology or related discipline

Descrizione del lavoro

Recordati S.p.A in Milano seeks Head of Quality Systems and Risk Management to lead global QMS and QRM across GMP manufacturing, laboratories, supply chain, distribution operations, contract partners and affiliates. You will act as corporate process owner for quality systems, ensuring compliance, inspection readiness, patient safety, product quality and continuous improvement across the organization.

Fluent in English; Bachelor degree in a related field and 12–15 years of pharma quality