Henry Schein

Quality & Regulatory Affairs EMEA

Henry Schein  •  Federal Republic of Germany (Onsite)  •  7 days ago
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Job Description

Join Team Schein in a meaningful EMEA Quality & Regulatory Affairs role where collaboration, integrity, and continuous improvement come together. You’ll partner across countries and functions to ensure compliance, support product readiness, and help deliver trusted healthcare solutions that make a real difference.

Your responsibilities will include:

  • Supports EMEA-wide QA/RA operations, documenting EMEA policies and provides support to implement the EMEA Quality Management System.

  • To provide comprehensive managerial and strategic ensuring efficient daily operations, effective communication, and seamless regional management of quality-related projects, compliance, and reporting.

  • Supports to perform quality & regulatory visits and /or audits to countries and issues gap analysis, ensures CAPA follow-up on identified issues and support countries in implementing solutions.

  • Participates to EMEA QA/RA Management meetings, issues minutes and follows-up on decided actions with related functional / country QA/RA Lead.

  • Organizing virtual, onsite, and offsite regional meetings, including logistics, agendas and close follow-up of identified actions.

  • Driving & supporting multiple projects, tracking timelines, and ensuring successful outcomes for EMEA-wide QA/RA initiatives.

  • Provides support to the PRRC of the EC Rep in Germany for Henry Schein Products by

  • Review Quality Agreements to ensure responsibilities of economic operators (Importer/Distributor) are clearly addressed.

  • Provides support to the Spanish QA/RA Team for Quality related topics to ensure compliance according GDP and MDR.

Your Qualification

  • Bachelor’s degree in Life Sciences, Pharmacist, Biomedical Engineering, or a related field with previous experience in Quality Management, Project Management, Medical Device and Pharmaceutical (GDP) experience is a plus

  • Support Communicating with Regulatory Bodies MDR /IVDR Regulations/ ISO 13485

  • Validation of (computerized systems) and Risk management (FMEA) knowledge is a plus

  • Experience in Quality System process implementation and maintenance to meet ISO 13485:2016; GDP and MDR.

  • You are solution oriented, have problem-solving attitude, and can be pragmatic, high adaptability and flexibility

  • Ability to work in a matrix, regional environment with different departments and countries

  • Fleuncy in English language and a good communication skills and stakeholder management

Henry Schein

About Henry Schein

Henry Schein, Inc. (Nasdaq: HSIC) is a solutions company for health care professionals powered by a network of people and technology. With more than 25,000 Team Schein Members worldwide, the Company's network of trusted advisors provides more than 1 million customers globally with more than 300 valued solutions that help improve operational success and clinical outcomes. Our Business, Clinical, Technology, and Supply Chain solutions help office-based dental and medical practitioners work more efficiently so they can provide quality care more effectively. These solutions also support dental laboratories, government and institutional health care clinics, as well as other alternate care sites.

Henry Schein operates through a centralized and automated distribution network, with a selection of more than 300,000 branded products and Henry Schein corporate brand products in our distribution centers.

A FORTUNE 500 Company and a member of the S&P 500® index, Henry Schein is headquartered in Melville, N.Y., and has operations or affiliates in 33 countries and territories. The Company's sales reached $12.7 billion in 2024, and have grown at a compound annual rate of approximately 11.2 percent since Henry Schein became a public company in 1995.

Industry
Manufacturing & Production
Company Size
10,000+ employees
Headquarters
Melville, NY
Year Founded
1932
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