Global M&S Services, Manager Quality Services - Third Party Audits, Budapest Hub
布达佩斯, 匈牙利 Regular 发布于 Jun. 23, 2026 申请截止于 Jul. 23, 2026 Salary Range HUF 10,944,000.00 - 16,416,000.00Job title: Global M&S Services, Manager Quality Services - Third Party Audits, Budapest Hub
Location: Budapest, Hungary
Approximately 30% of travel expected
Job type: Permanent, full time
Hybrid working (60% office, 40% home)
About the job
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Join our Global Manufacturing and Supply Services Team as Senior Manager Quality Services and you can help make it happen. Our team 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. The team members of Global M&S Services Hubs will act as partners in carrying out tasks and fulfilling responsibilities to support identified and established global quality processes from the hubs.
Your job? You will be responsible for acting as partners to M&S organization in carrying out tasks and fulfilling responsibilities to support identified and established global quality processes from the hubs.
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.
Main responsibilities:
Provide QA and Technical Support to Third Party Manufacturers (TPM) and Contract Manufacturer Organization (CMO), TPM/CMO Operations, Affiliates, and other Stakeholders.
Responsible for compliance with Corporate and Divisional QA policies, procedures, standards, and specifications as well as country specific regulations depending on the TPM location and markets.
Ensure compliance to Corporate and Divisional QA requirements and identify and / or resolve Quality gaps and / or issues relating to product design, manufacturing quality programs and product start-ups at TPMs.
Responsible for overall quality and safety of products manufactured at those facilities.
Utilize understanding of QA systems and problem-solving tools to provide alternative solutions to quality issues.
Manage supplier audits, ensuring cGMP and SOP alignment.
Track market developments, regulatory changes.
Follow up on CAPAs.
Participate in audits, inspections, interface with specialists.
Provide an assessment of supplier’s quality in place with regards to material compliance, as well as regulatory of CAPA before communicating it to be the request sites.
Being a local quality contact between the Suppliers, Global Quality Suppliers & IA sites to facilitate follow up of improvements and exchange of quality information.
Support audits lead by other auditors when specific expertise is needed (e.g. for cause audit with user sites representatives, highly sophisticated topic)
Conduct on-site and remote audits of GxP and Health Regulated Third Party vendors to ensure compliance with regulations and company policies.
Collaborate with stakeholders regionally for inspection preparedness.
About you
Experience:
4+ years of Compliance or Auditing experience.
7-10 years of related experience in the pharmaceutical industry.
Thorough knowledge of cGMPs, Code of Federal Regulations in drugs and biologics.
Should be knowledgeable in Quality functions of pharmaceutical industry.
Experience in conducting on site audits, inspections and facing regulatory/health authority inspections/audits.
Thorough knowledge of CAPA systems is required and experience is desirable.
Thorough knowledge of and experience in application of GMP requirements.
Experience managing third party manufacturers and/or contract manufacturer organization is preferred.
Experience working on manufacturing sites is an added advantage.
Technical skills:
Knowledge of cGMPs.
Knowledge of Code of Federal Regulations in drugs and biologics.
Knowledge of CAPA systems is required and experience is desirable.
Knowledgeable in Quality functions of pharmaceutical industry.
Soft skills:
Excellent problem solving and decision-making skills are critical to this position.
Proficient in problem-solving, attention to detail, and good organizational skills.
Work in a team-oriented, flexible, and proactive manner.
Analytical skills and ability to multitask in a stressful environment.
Education: Master’s or Ph.D. in Life Sciences/Healthcare, or related technical field.
Languages: Excellent knowledge of English language (spoken and written).
Why choose us?
Bring the miracles of science to life alongside a supportive, future-focused team in an international work environment
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave
An individual and well-structured introduction and training of new employees and we will dedicate a Buddy for you to better navigate in your first weeks
Join a great community & special events (Monthly Board Game Nights, Well-Being Lectures & Sport Clubs)
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).
PursueProgress. Discover Extraordinary.
Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
Discover our Code of Conduct, that serves as the moral compass that guides us when chasing the miracles of science to improve people’s lives. Please ensure to have read this document before applying.
#Sanofi #SanofiCareers #joinSanofi
#jobopportunities #careeropportunities #sscjob
#Sanofi_Budapest_Hub #Budapest
#LI-EUR #LI-hybrid
追寻 发展。探索 菲凡。
进步需要我们每个人的参与——不论其背景、地域、或职业,我们都有一个共同的愿望:创造奇迹。你也可以成为其中的一员。我们不断追求变革,拥抱新思想,探索我们所能提供的一切机会。让我们一起追求进步。共同发现非凡。
在赛诺菲,不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同,我们为所有人提供平等的机会。
观看 “在赛诺菲的一天” ,并在官网 (sanofi.com) 上查看赛诺菲的多元化、公平与包容倡议!
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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心怀梦想,成就一番事业
我们希望您以饱满的热情投入到自己的工作岗位中,给全球数百万人带来美好生活。您的职业发展道路由您自己来掌控。您只管制定目标,我们会提供充足的培训机会和支持,让您得偿所愿。
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我们关注每一个员工的声音。因为,我们的未来取决于所有员工的付出与努力。正因为他们的助力,我们才能追求远大的理想。