Head of Site Quality

Reposted 11 Hours Ago
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Miskolc, Miskolci Járás, Borsod-Abaúj-Zemplén
In-Office
Senior level
Healthtech
The Role
The Head of Site Quality will implement quality policy, ensure regulatory compliance, drive quality performance, and lead a quality team focused on delivering compliant products.
Summary Generated by Built In

About the job

As Head of Site Quality, you’ll be responsible for implementing Sanofi's Quality Policy, ensuring regulatory compliance, and driving quality performance across all site operations while serving as the primary quality representative to Health Authorities. The role encompasses strategic quality leadership including batch release decisions, inspection readiness, manufacturing license maintenance, and developing a high-performing quality team to ensure products are delivered with the right quality, on time, and in full regulatory compliance. Ready to get started?

About Sanofi:

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main responsibilities:

  • Preparation of quality strategy plan and implementation of the Sanofi Quality Policy at site, according to regulatory requirements
  • Driving site quality performance and business continuity
  • Ensuring the release of products manufactured at site, with the right quality and at the right time in compliance with regulation
  • Nominate Quality person for batch disposition
  • Representing Site Quality in front of Health Authorities
  • Ensuring application and maintenance of the site manufacturing license
  • Driving site inspection readiness
  • Developing and engaging site quality team with the right quality skills, mindset, leadership, and culture
  • Define site quality risk management program and involved in related decisions for remediation
  • Decide on product quality event reportability and maintain the Site Master File
  • Ensure adequate GMP training of site employees
  • Operational management of site Quality management organization including Quality Control, Quality Assurance, Quality system and Compliance as well as Regulatory department
  • Strong interaction with sister sites within the cluster
  • Monitoring of regulatory changes, new authority requirements in the EU, WHO, ANVISA, EAEU, other regulatory region
  • Active participation in Global or HUB projects, initiatives

About you:

  • Experience: Strong experience in assurance, quality management in the pharmaceutical industry, including in the development, review, and approval of quality system documents
  • Experience in authority inspection, capability in communication with Authority representatives
  • Experience  in risk management and simplification, harmonization
  • Education: Preferably degree in Pharmacy, or degree in Chemistry, Biochemistry, Biotechnology, Chemical engineer or Microbiologist eligible for registration as a Qualified Person
  • Soft and technical skills:
  • Strong knowledge in GMP and related regulation in min. EU region, but preferably knowledge in EAEU, WHO, ANVISA regulations
  • Operational understanding of aseptic manufacturing, especially knowledge in EU GMP Annex 1 regulation
  • basic knowledge in Microbiology
  • Technical skills ability to meticulously review and manage documents to ensure accuracy, completeness, and compliance with regulatory standards
  • Demonstrated experience in managing one or several quality systems and processes in the past with team management experience
  • project management skills
  • capability of risk taking
  • experience in efficiency improvement, digitalization projects
  • good leadership skills, talent development
  • Languages: Hungarian and English (fluent)

#LI-EUR

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!

Top Skills

Gmp
Quality Management Systems
Regulatory Compliance
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The Company
HQ: Paris
85,000 Employees
Year Founded: 1973

What We Do

We are Sanofi, an innovative global healthcare company. We chase the miracles of science to improve people’s lives.

Our team, across some 100 countries, is dedicated to transforming the practice of medicine by working to turn the impossible into the possible. We provide potentially life-changing treatment options and life-saving vaccine protection to millions of people globally, while putting sustainability and social responsibility at the center of our ambitions.

Interactions with this account must comply with the Terms: https://bit.ly/sanofi-terms

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