Sanofi

Sanofi

Posted via Workday

Quality Validation Manager IFF (all genders)

Apply by Nov 16, 2026

Posted Oct 20, 2026

Role at a glance

Job function
Manufacturing & Skilled Trades Quality Assurance & Quality Control
Salary
Not yet verified Check the description for pay details; an amount or pay period has not been verified.
Location
Frankfurt am Main
Employment
Full-time
Education
Ideally Masters/Diploma Degree in Science, Pharmacy or Equivalent

Spotted an issue?

We’ll check it against the original posting.

Log in to report

Role Summary

AI-generated

The Quality Validation Manager IFF is responsible for ensuring the project’s Quality Qualification and Validation activities meet project, local, global, and regulatory requirements. The role supports quality execution from detailed design and construction through qualification, validation, and future site organization readiness.

What You'll Do

  • Serve as the project Quality subject matter expert for Qualification and Validation.
  • Deliver quality activities to project plans and needs, including writing, reviewing, and releasing documentation using a QbD approach as...
  • Contribute to QMS improvements and develop, update, and promote global quality documentation and procedures.
  • Ensure consistency of turnover packages to system owners.
  • Support execution of project qualification and validation strategies and plans, and collaborate with the facility in China to share best...
  • Participate in project meetings and planning sessions to support effective planning and execution of Quality Validation deliverables.

Generated from the employer's posting. Verify important details before applying.

View full posting

Qualifications

Relevant experience within the industry; in-depth knowledge of biologic product license (BLA) application registration process and associated regulatory requirements. Skills and experience include quality systems, qualification and validation activities (e.g. Cleaning Validation, Filter Validation, Analytical Validation), continuous improvement management, GxP and health-regulated expertise, international and FDA exposure, and the listed communication, leadership, decision-making, collaboration, negotiation, business partnering, and people-development skills. Proficiency in German and English is required.

Preferred

  • Ideally Masters/Diploma Degree in Science, Pharmacy or Equivalent
  • Biopharma and/or related regulated industry experience, preferably in Insulin DS processes

Original job description

Content provided by the employer

To ensure a rapid processing of your application, please apply only via the “Apply” button. Please include a letter of motivation and a current resume with your application.



About the job

Be part of a once-in-a-generation project that’s shaping the future of insulin. 

Sanofi is building a cutting-edge, fully automated insulin drug substance facility in Frankfurt – a bold investment that builds on our legacy of excellence in insulin manufacturing. This sustainable, next-gen biologics site will support the entire portfolio of insulins, from development to delivery. 

Join us at the forefront of this global transformation. As part of a cross-functional program team, you’ll help bring this facility to life – from early design and construction through to readiness for commercial manufacturing. Your work will help turn the miracles of science into reality for millions living with diabetes. 

Meet Katrin, our Global Insulin Program Leader, and see how we’re reimagining insulin production. Watch now! 


Position overview

The Quality Validation Manager IFF is responsible for ensuring that all aspects of Quality Qualification and Validation activities for the project are executed on time and in accordance with the project, local and global requirements, and applicable regulations.

As an integral part of the project quality team, this position has overall responsibility for participating in project workstreams, ensuring proper execution of all qualification and validation strategies and providing support and guidance for quality processes and procedures.

This role is expected to work independently and with a level of autonomy and authority in decision-making to ensure on-going compliance against approved documents and current Good Manufacturing Practices across the project during technical detailed design, construction, C&Q, PQ, validation phases and future site organizations until final approval within worldwide dossiers.


Main responsibilities:

  • Ensure quality culture, mindset, GMP compliance performance and continuous improvement across all functions and organizational levels across the project and future sites. 
  • Serve as Quality Subject Matter Expert (SME) for the project on all matters related to Quality Qualification and Validation, ensuring quality compliance in project execution. 
  • Deliver Quality activities in accordance with IFF planning & project needs, including writing, reviewing and releasing documentation considering QbD approach as required. 
  • Contribute to the improvement of QMS initiatives to ensure compliance with applicable regulatory requirements and Sanofi quality standards at all times. 
  • Develop, update and promote Sanofi Global Quality Documentation and IFF GOPs or Global procedures. 
  • Ensure the consistency of turnover packages to system owners. 
  • Support execution of project Qualification, Validation strategy and plans as required whilst Collaborate with the facility in China to maintain benchmark standards and share best practices
  • Actively engage in project team meetings, planning sessions, and related project requirements to ensure effective planning and execution of key Quality Validation deliverables

About you

  • Education/Experience: Ideally Masters/Diploma Degree in Science, Pharmacy or Equivalent;  relevant experience within the industry, preferably within biopharma and/or related regulated industry, preferably in Insulin DS processes; In-depth knowledge of biologic product license (BLA) application registration process, and the associated regulatory requirements. 
  • Soft and technical skills: Act for Change, Cooperate transversally, Decision making, People Development, Thoughtful-Risk-Taking mindset, Negotiation and Influential skills, Business Partnering, Communication skills (English), Leadership and assertiveness skills ; experience with Quality systems, Qualification & Validation activities (e.g. Cleaning Validation, Filter Validation, Analytical Validation), Continuous improvement management, GxP and health-regulated expertise, international and FDA exposure 
  • Languages: proficiency in German and English required

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 :€80.724,00 - €121.068,00

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.

Sanofi

About the company

Sanofi

Large Enterprise

Sanofi is a global healthcare leader committed to promoting health and well-being through the development of innovative medicines, vaccines, and therapeutic solutions. With a diverse portfolio that spans multiple therapeutic areas, including diabetes, oncology, and immunology, Sanofi is dedicated to addressing pressing health challenges and improving patient outcomes worldwide. Headquartered in France, the company employs over 100,000 individuals across more than 100 countries, fostering a culture of collaboration and scientific excellence to drive advancements in healthcare.