Quality Control Supervisor, Instruments

Obsessed by Science. Entrepreneurial by Nature. United by Purpose.

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions, advancing science to improve patient outcomes worldwide. For more than 50 years, we have combined scientific rigor with an entrepreneurial mindset, operating with a strong commitment to innovation, accountability, and results to deliver trusted diagnostic solutions.

As the Diagnostics Specialist, Diasorin continuously invests in research, technology, and people. Guided by our values of operational excellence, customer focus, and teamwork, we empower teams to think boldly, act decisively, and transform ideas into meaningful impact across one of the industry's broadest specialty diagnostic portfolios.

When you join Diasorin, you are not just filling a role. You are helping build what comes next.

Why Join Diasorin

• Build What Matters
  Take ownership, challenge the status quo, and contribute directly to solutions that improve patient care worldwide.
• Innovate with Agility at a Global Scale
  Work in an entrepreneurial environment that enables speed, collaboration, and global impact.
• Grow in a People-Centered Culture
  Thrive in a culture that values accountability, inclusion, and continuous development.

Job Scope

Quality Control Supervisor, Instrument - 2 will be responsible for:

• Provides direct supervision to the incoming inspection personnel and assures the effective use of all the resources to meet goals and requirements set forth by the Company and by Regulatory entities.
• Ensures Safety, Quality, GMP, ISO, and housekeeping standards are adhered to
• Provides technical support and process improvement to minimize cost and increase productivity.
• Plays a key role in Lean Manufacturing Implementation.
• Supervises difficult inspection processes problems through a well and sound solution methodology

Key Duties and Responsibilities

• Ensures proper incoming inspection of components, packaging materials and final product in compliance with company procedures and ISO/FDA/GMP standards
• Reviews inspection, labeling, and release logistic for appropriate process flow and documentation.
• Updates drawing, inspection procedures and any other documentation needed to inspect, test or purchase products
• Oversees supplier quality metrics including but not limited to first pass yield.
• Collect and analyze data to track improvement and develop appropriate corrective actions, Conduct analysis, inspection, and trending in accordance with inspection plans work instructions and other quality standards to assure the quality of product or components
• Supervise personnel in incoming inspection area to assure control, adherence to safety, quality, and schedule requirements
• Coordinates subordinate work to achieve result associated with daily business schedule and goals as assigned
• Support and execute quality goals and initiatives
• Interacts with suppliers, vendors, and/or customers when needed to support business needs
• Develops, establish and continuously improve the necessary controls around incoming inspections when needed to support new and existing products.
• Motivates, supervises and develops personnel in a team environment
• Investigate and manage NCMRs including investigation, additional testing, test analysis, disposition, and ERP inventory management reconciliation and follow up on issued Corrective Actions
• Ensures results are recorded on inspection forms and reports number of defects found
• Maintains department files for readily retrievable access of records
• Ensures good documentation practices during document review and inspection
• Ensure incoming parts are inspected according to blue-print & drawing specifications
• Other duties as assigned

Education and Experience Qualifications

• Bachelor's Degree in Life Science or Engineering discipline
• 5 years of relevant experience in a hardware manufacturing environment in an FDA regulated industry and/or ISO certified organization with a Bachelor's Degree; preferred
• 8 years of relevant experience required with an Associate Degree. preferred
• 2 years of relevant Manufacturing Operations leadership experience. preferred

What we offer

Receive a competitive salary and benefits package as you grow your career at Diasorin. Join our team and discover how your work can impact the lives of people all over the world.

Diasorin is committed to building a workplace where people feel empowered to contribute ideas, take ownership, and grow their careers. We believe diverse perspectives strengthen innovation and help us deliver meaningful impact for patients and customers worldwide.

Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by applicable law.

This posting and recruitment process are subject to applicable local laws and regulations in the country where the position is located. Additional employment disclosures, candidate rights, and employment conditions may apply based on local jurisdiction.

Individuals hired will be required to verify identity and eligibility to work and may be subject to a background check and drug screening where permitted by law. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities during the application process. If assistance is required, please contact View email address on click.appcast.io.

Recruitment Fraud Notice

Diasorin never requests payment, financial information, or personal banking details from candidates at any stage of the recruitment process. Official communications from Diasorin recruiters will only come from a verified @diasorin.com email address. If you have questions about the legitimacy of a recruitment communication, please contact View email address on click.appcast.io for verification.

Unauthorized third-party recruiting agencies may not submit candidates for this position without prior written authorization from the Diasorin Human Resources Department.