CHINOIN Private Co, Ltd Posted August 19, 2026

Global M&S Services, Manager Quality Services - Third Party Audits, Budapest Hub

Budapest, Hungary Full time
Quality Manager
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CHINOIN Private Co, Ltd is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job title: Global M&S Services, Manager Quality Services - Third Party Audits, Budapest Hub

Location: Budapest

Job type: permanent, full time

Travel required as per job demands

Hybrid working

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 Manager Quality Services – Third Party Audits and you can help make it happen. Our mission is to deliver and support Global M&S teams in partnership with Business and Digital, and drive priority and transformative initiatives across the organisation.

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 of working on manufacturing sites is an added advantage.

Skills:

Excellent problem solving and decision-making skills are critical to this position.  The successful candidate must be able to demonstrate their risk-based decision-making ability.

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

Work from an "Office of the Year 2025" award winner with flexible home office policy

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, Summer Events, 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

#Sanofi_Budapest_Hub #Budapest

#R&D

#LI-EUR #LI-hybrid

Pursue progress , discover extraordinary

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 - Ft14 592 000 Final 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.

Job details

Seniority
Manager
Function
Quality
Therapeutic area
Not listed
Location
Budapest, Hungary
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 246 comparable Manager Quality roles across 80 biopharma companies.

246Comparable roles tracked
230Currently active
80Companies hiring similar roles
33Countries represented

Salary context

59 of 246 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Quality Control Associate Scientist- Overnight Shift · Merck KGaA $27/hr – $46/hr (≈ $56,160–$95,680/yr)
Peer group range $75,920 – $208,845 (median $175,750)

Where these roles are based

Top locations among the 246 comparable roles

United States88
China27
India16
Ireland16
Japan12
United Kingdom7

+ 27 more countries

Seniority mix

246 of 246 peers have a known seniority level

Manager181
Associate Director42
Associate23

Therapeutic area mix

1 of 246 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Rare Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Mylan Hungary Kft. Komárom, Hungary Manager
Same function Same seniority Same country
60%similar
CHINOIN Private Co, Ltd Budapest, Hungary Manager
Same function Same seniority Same country
45%similar
AbbVie North Chicago, IL Manager
Same function Same seniority
45%similar
Novartis Carlsbad, United States Manager
Same function Same seniority
45%similar
Gilead Sciences K.K. Tokyo, Japan Manager
Same function Same seniority
45%similar
Gilead Sciences, Inc. Foster City, United States Manager
Same function Same seniority

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Interim Release QP Manager
Mylan Hungary Kft. · Komárom, Hungary · Manager
Function Therapeutic area Seniority Country
45%
Manager, QA Method Validation
Novartis · Carlsbad, United States · Manager
Function Therapeutic area Seniority Country
45%
Senior Manager, Quality Assurance
Gilead Sciences, Inc. · Foster City, United States · Manager
Function Therapeutic area Seniority Country
45%
CSV Manager
Mylan Teoranta · Inverin, Ireland · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.