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Regional Qualification Senior specialist

布达佩斯, 匈牙利 Regular 发布于   Aug. 12, 2026 申请截止于   Oct. 12, 2026 Salary Range   HUF 7,603,200.00 - 11,404,800.00
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  • Location: Budapest, Hungary
  • Flexible working: hybrid

Our Team:

Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions.

As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability & interoperability and thus accelerate impact on global health.

Global Manufacturing & Supply (M&S) Services is responsible for delivering and supporting Global M&S teams in partnership with Business and Digital, and drive priority and transformative initiatives across M&S Services. The team members of Global M&S Services (Report Issuance) will act as partners in carrying out tasks and fulfilling responsibilities to support identified and established Global Quality processes from the hubs.

The Qualification & Validation Report Issuance team performs report writing, review, documentation, planning, and execution tracking for equipment (re)-qualification, Quality Review for Standard equipment’s across sites.

Main responsibilities:

  • Write (re)qualification protocol/report for manufacturing site facilities, utilities and equipments according to their categorization type and requirements
  • Takes part in data collection regarding the dedicated site facilities, utilities and equipments
  • Check if parameters, operating conditions, and acceptance criteria are defined in the protocol per Standard Operating Procedure. Ensure data integrity and quality rules are correctly captured
  • Connect with experts to review and discuss analysis results, determine if the objective of the study has been met. 
  • Check the list of deviations and change controls, identify the ones which might have an impact on the qualified status of the facilities, utilities or equipments.
  • Define findings, make conclusion after interpretation of all needed data and information
  • Ensure that content of the qualification reports complies with regulatory requirements (e.g., FDA, EMA), GxP and company quality standards.
  • Cooperate with cross-functional teams (regional manufacturing sites, global and other regional HUBs and specific project teams) to ensure smooth execution of issuance of (re)qualification reports.
  • Perform tasks in accordance with Good Manufacturing Processes and Health, Safety, Environment requirements and with the associated instructions, procedures, records related to these tasks.  
  • If applicable, translate the manufacturing data package
  • Participate continuous improvement initiatives through standardization, simplification, and digitalization of equipment qualification processes

About you:

  • Experience: Professional experience in pharma industry (GxP regulated environment)
  • Soft skills: Proficient in problem-solving, attention to detail, and good organizational skills. Ability to work collaboratively with cross-functional teams in a flexible and proactive manner. Strong analytical skills. Agile thinker and learner, adaptable to complex & dynamic environments
  • Technical skills: Quality systems (e.g., Veeva, Kneat), Word, Excel, Power Point
  • Education: Bachelor's degree (preferably in engineering, pharmacy, chemistry, biology, or related field)
  • Languages: Excellent English communication and writing, proficiency in one of the listed languages preferred: French, German, Italian, Hungarian.

Be part of something exceptional. Our Budapest Hub has been recognized for workplace excellence, innovation, and our commitment to putting people first. See the full list of our awards at the end of this posting.

  • Office of the Year 2025 – Evolution Award
  • Our most recent award – Sanofi is recognized for creating an innovative workspace that supports collaboration and adaptability.
  • Marketing Diamond Award 2026 – Employer Branding
  • One of the highest honours at Hungary's prestigious Marketing Diamond Awards, recognizing excellence in employer branding.
  • BSC Investor of the Year 2025
  • Awarded by HIPA, ABSL Hungary, and AmCham Hungary for our contribution to Hungary's business services sector.
  • PwC Workforce Preference Survey 2025 – Top 3 Most Attractive Employers
  • Ranked 3rd among the most attractive employers in Hungary.
  • Hungarian Employer Branding Awards 2025 – Gold & Silver
  • Best Strategic Employer Branding Campaign (Gold) and Best Employer Branding Campaign in the Pharma Sector (Silver).

追寻 发展探索 菲凡

加入赛诺菲,开启科学新时代。在这里,你的成长将如我们的工作成果一样具有变革性。我们帮助你发展,助你走得更远、思考得更快、做前所未有的事。你将与我们一起突破边界、挑战常规,打造更智慧的解决方案,惠及全球社区。准备好追寻科学的奇迹,改善人们的生活了吗?让我们携手追寻发展,探索非凡。

赛诺菲致力于为所有员工提供平等的就业机会,不因种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾、性别认同、受保护的退伍军人身份或其他受法律保护的特征而有所差异。

最终薪酬将根据已展现的经验、技能、工作地点和其他相关因素确定。员工可能有资格参与公司员工福利计划。

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