Quality Control Expert

Fresenius Medical Care

Palazzo Pignano

In loco

EUR 28.000 - 36.000

Tempo pieno

2 giorni fa
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Vantaggi offerti da questo lavoro

International healthcare company
Continuous learning
Dynamic and collaborative environment
Exposure to cross-functional projects

Descrizione del lavoro

Fresenius Medical Care in Palazzo Pignano, Italy, seeks a proactive Quality Control Expert to support the QC Manager and oversee QC operations in a highly regulated manufacturing environment.

You will coordinate inspections, testing, documentation, and release of materials, while collaborating with Production, Engineering, and Supply Chain to ensure patient safety and product quality. English proficiency required.

Competenze

  • Minimum 2 years in quality control or similar role.
  • Experience in regulated manufacturing environments is preferred.
  • Basic knowledge of quality systems and documentation.

Mansioni

  • Support the QC Manager in planning, organizing, and coordinating Quality Control activities.
  • Coordinate day-to-day QC operations, aligning with production timelines and SAP release schedules.
  • Ensure proper QC on incoming materials, components, semi-finished and finished products.
  • Review and approve QC documentation and batch records.
  • Release semi-finished products to the next manufacturing phase.
  • Manage non-conformities, customer complaints and change controls.
  • Coordinate outsourced microbiological testing and environmental monitoring.
  • Collaborate with cross-functional teams to drive improvements.
  • Assist training within the QC team and act as deputy during absences.

Conoscenze

English proficiency (B1/B2)
Analytical mindset

Formazione

Scientific high school diploma or equivalent technical qualification

Strumenti

Microsoft Office

Descrizione del lavoro

  • Quality Control Expert

    Location: Palazzo Pignano (CR), Italy
    Employment Type: Full-time

    At Fresenius Medical Care, we are the global leader in kidney care, committed to improving the lives of patients with chronic kidney disease. Our mission is to deliver high-quality, innovative products, services, and care across the entire healthcare journey. Guided by our vision—“Creating a future worth living. For patients. Worldwide. Every day.”—we work with purpose and compassion, supported by a global team of over 125,000 employees.

    Within our Care Enablement segment, we develop and provide life-sustaining medical products, digital health solutions, and therapies that empower clinical teams and improve patient outcomes. Our FME Reignite strategy drives transformation through innovation, efficiency, and sustainable growth.

    Our values guide how we work:

    • We Care for our patients, each other, and our communities

    • We Connect across teams and borders to deliver excellence together

    • We Commit to doing things the right way— growing with purpose and leading kidney care with integrity and innovation

    Information about plant

    Located in northern Italy, our Palazzo Pignano plant serves as a key center for the production and development of dialysis-related medical devices. With more than 550 employees, the plant specializes in manufacturing both peritoneal dialysis (PD) disposables and hemodialysis (HD) bloodline components. It combines large-scale production capabilities with strong R&D and engineering expertise. By utilizing advanced technologies to ensure the highest standards in dialysis product manufacturing, we’re not only driving innovation — we’re also creating meaningful change for patients worldwide.

    Join our passionate team and be part of this global impact!

    About the role

    We are looking for a proactive and detail-oriented Quality Control Expert to join our Quality team.

    In this role, you will support the Quality Control Manager in coordinating daily QC operations, ensuring compliance with quality requirements, and maintaining continuity of departmental activities. You will play a key role in overseeing incoming inspections, in-process controls, finished product testing, sterilization activities, and microbiological testing managed through external laboratories.

    The position offers the opportunity to work in a highly regulated manufacturing environment, collaborating closely with Production, Engineering, Industrialization, Supply Chain, Quality Assurance, and Supplier Quality teams to ensure the highest standards of product quality and patient safety.

    Your responsibilities

    As Quality Control Expert, you will:

    • Support the QC Manager in planning, organizing, and coordinating Quality Control activities.

    • Coordinate day-to-day QC operations, setting priorities and ensuring alignment with production timelines and SAP release schedules.

    • Ensure the correct execution of quality controls on incoming materials, components, semi-finished products, and finished products.

    • Review and approve quality control documentation and batch records.

    • Release semi-finished products to the next phase of the manufacturing process.

    • Manage non-conformities, customer complaints, SNCRs, process changes, and special permissions.

    • Coordinate outsourced microbiological testing activities, including analysis planning, result review, deviation management, environmental monitoring, and cleanroom revalidation.

    • Collaborate with cross-functional teams to investigate issues and drive continuous improvement initiatives.

    • Support training and development activities within the QC team.

    • Act as deputy for the QC Manager during absences, ensuring operational continuity.

    • Support validation activities and the introduction of new products, materials, and processes.

    • Participate in the review and validation of analytical methods where applicable.

    What you'll bring

    Required qualifications

    • Scientific high school diploma or equivalent technical/scientific qualification.

    • Minimum 2 years of experience in a Quality Control environment or in a comparable quality-related role.

    • Good command of English (B1/B2 level).

    • Good knowledge of Microsoft Office applications.

    • Strong technical mindset and hands-on approach.

    • Good organizational and problem-solving skills.

    • Ability to work independently and effectively collaborate with cross-functional teams.

    Preferred qualifications

    • Degree in a scientific discipline or Engineering degree with a scientific focus.

    • Experience in regulated manufacturing environments, preferably medical devices, pharma, healthcare, or related industries.

    • Knowledge of quality systems, validation activities, and laboratory coordination processes.

    What we offer
    • Opportunity to grow within an international healthcare company.

    • Continuous learning and professional development opportunities.

    • Dynamic and collaborative work environment.

    • Exposure to cross-functional projects and quality improvement initiatives.

The indicative annual base salary range for this position is between €28,000 and €36,000.

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