Budapest, Central Hungary, Hungary · Hybrid
$10944k–$16416k/yr
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Budapest, Central Hungary, Hungary · Hybrid
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Budapest, Central Hungary, Hungary · On-site
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Budapest, Central Hungary, Hungary · On-site
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Budapest, Central Hungary, Hungary · On-site
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Budapest, Central Hungary, Hungary · Hybrid
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Budapest, Central Hungary, Hungary · Hybrid
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Budapest, Central Hungary, Hungary • Hybrid
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The role involves providing QA and technical support to third-party manufacturers and CMOs to ensure compliance with corporate policies and global regulations. Responsibilities include managing supplier audits, tracking regulatory changes, and resolving quality gaps in product design and manufacturing.
Candidates need a Master's or Ph.D. in Life Sciences or a related field with 7-10 years of pharmaceutical industry experience. A minimum of 4 years in compliance or auditing and thorough knowledge of cGMP and CAPA systems are required.
Job 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.
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.
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).
Pursue Progress. 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
#SanofiBudapestHub #Budapest
#LI-EUR #LI-hybrid
Better is out there. Better medications, better outcomes, better science. But 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. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
The salary range for this position is :Ft10 944 000,00 - Ft16 416 000,00Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in Company employee benefit programs.
We are an R&D driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. We apply our deep understanding of the immune system to invent medicines and vaccines that treat and protect millions of people around the world, with an innovative pipeline that could benefit millions more. Our team is guided by one purpose: we chase the miracles of science to improve people’s lives; this inspires us to drive progress and deliver positive impact for our people and the communities we serve, by addressing the most urgent healthcare, environmental, and societal challenges of our time. Interactions with this account must comply with the Terms: https://bit.ly/sanofi-terms
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There are currently 245 open manufacturing positions in Budapest, Hungary listed on Clera. New openings are added daily as companies post roles.
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