Global Supplier Quality Senior Specialist

Milano 11-12-2025

Global Supplier Quality Senior Specialist

Alfasigma Milano 11-12-2025
Riassunto

Località

Milano

Divisione Aziendale

Tipo di contratto

Data di pubblicazione

11-12-2025

Descrizione Lavoro

Global Supplier Quality Senior Specialist
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The Senior Specialist, Global Supplier Quality is responsible for driving supplier qualification, monitoring, and compliance activities across the global supply chain. This role plays a critical part in ensuring that all suppliers of raw materials, components, and services consistently meet regulatory, quality, and safety requirements.
Acting as a key interface between internal stakeholders and external suppliers, the Senior Specialist will champion quality excellence, risk mitigation, and continuous improvement to strengthen the company’s global quality network and ensure business continuity.
Key Responsibilities
Lead global supplier qualification, approval, and requalification processes in alignment with corporate and regulatory standards.
Develop and maintain comprehensive supplier risk assessments and qualification documentation.
Oversee the full supplier lifecycle — from onboarding and performance monitoring to periodic reviews and requalification.
Audits & Compliance
Plan, conduct, and report supplier audits (both on-site and remote) to verify compliance with internal and external standards.
Ensure adherence to GMP, ISO 13485, HACCP, and other applicable global quality and regulatory frameworks.
Partner with suppliers to address audit findings, implement corrective and preventive actions, and monitor their effectiveness.
Documentation & Quality Systems
Support site quality operations in reviewing and approving supplier-provided documentation, including change controls, technical files, and periodic reviews.
Maintain and update Supplier Quality Agreements, ensuring alignment with internal policies and regulatory requirements.
Contribute to the preparation and successful execution of regulatory inspections and customer audits related to supplier management.
Risk Management & Continuous Improvement
Proactively identify and mitigate supplier-related risks impacting product quality or supply continuity.
Drive supplier performance improvement initiatives to enhance quality, reliability, and compliance maturity.
Monitor supplier KPIs, conduct performance reviews, and promote a culture of continuous improvement.
Cross-Functional Collaboration
Collaborate closely with Procurement, Manufacturing, R&D, and Regulatory Affairs to ensure alignment on supplier quality strategy and standards.
Provide expert guidance, training, and support to internal teams on supplier qualification, compliance, and audit processes.
Qualifications
Minimum 7 years’ experience in supplier quality management within pharmaceuticals, medical devices, or food supplements.
Strong working knowledge of GMP, ISO 13485, HACCP, and global regulatory expectations.
Demonstrated success in supplier audits, risk-based quality management, and compliance oversight.
Lead Auditor certification highly desirable.
Bachelor’s or Master’s degree in Pharmacy, Chemistry, Engineering, or a related technical field.
Proven experience using digital tools and systems for supplier qualification and performance management.
Exceptional communication, stakeholder management, and problem-solving skills.
Ability to operate effectively in a fast-paced, matrixed, and multicultural environment.
Fluency in English required; additional languages are a plus.
Strong proficiency with Microsoft Office Suite and other business platforms.
Strategic, analytical, and results-oriented mindset with a commitment to quality excellence.
Seniority level

Mid-Senior level

Employment type

Full-time

Job function

Quality Assurance, Research, and Science
Pharmaceutical Manufacturing

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