Sanofi
Quality Manager / Qualified Person deputy page is loaded## Quality Manager / Qualified Person deputylocations:
Kievtime type:
Vollzeitposted on:
Heute ausgeschriebentime left to apply:
Enddatum: 10. November 2025 (Noch 27 Tage Zeit für Bewerbung)job requisition id:
R2826512*About the job***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:*** Act as Qualified Person back-up for importing license. Ensure compliant market batch release according to local regulation* Support the CQH to ensure robust system for GxP and health-regulated activities in compliance with Sanofi standards and with applicable local regulatory requirements.* Support Quality culture & promote Quality mind-set into the country governance, working principles and ways of operating.* Support quality oversight on country local contract manufacturers, distributors and GxP service providers.* Act as contact person for local health authorities for topics linked to quality control of product in Ukraine.* Support a process for management of GxP documents and records is in place in all GxP processes, considering data integrity principles.* Support information sharing, training sessions or programs related to processes under the responsibility of country quality for concerned country associates.* Support country regulatory inspections under quality responsibility, GMP regulatory inspection on manufacturing sites, country quality audits and provide support to other GxP country functions in country regulatory inspections for processes in their respective areas of responsibilities* Support inspection readiness and continuous quality improvement.* Support quality of products is managed according to Sanofi standard and local regulation* Support quality agreements with manufacturers, distributors (internal & external).*About you** 2 years’ experience with QMS in pharmaceutical industry (distribution and re-packaging experience is advantage).* Some experience with Import license is required* Knowledge of Good Distribution/Manufacturing guidelines/legislation. Knowledge of other GxP guidelines would be an advantage.* 1 years’ experience with batch release is advantage.* University qualification: Completed higher education (master level). Degree in Pharmacy is preferred, other degrees: Chemistry, Chemical Technology and Engineering, Biotechnology and Bioengineering, Biomedical Engineering, Biology or another life science discipline.* Analytical skills, ability to communicate with internal and external stakeholders, result-oriented team player* Ukrainian and English – advanced level both oral and written* Bring the miracles of science to life alongside a supportive, future-focused team.* Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.* 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.#LI-EUR**Pursue** *Progress*. **Discover** *Extraordinary*.Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before.*Progress* and 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, gender identity, protected veteran status or other characteristics protected by law.Diversity und Inklusion sind in den Grundwerten von Sanofi verankert und spiegeln sich in unserer Arbeitsweise wider. Wir respektieren die Vielfalt unserer Belegschaft in Hinsicht auf ihre Herkunft, Erfahrungen und Lebensweisen. Wir erkennen die Bereicherung, die diese Vielfalt birgt, und fördern Inklusion sowie
eine Arbeitsumgebung, in der diese Unterschiede sich weiter entwickeln können, zur Stärkung des Lebens unserer Mitarbeiter, Patienten und Kunden. #J-18808-Ljbffr
Kievtime type:
Vollzeitposted on:
Heute ausgeschriebentime left to apply:
Enddatum: 10. November 2025 (Noch 27 Tage Zeit für Bewerbung)job requisition id:
R2826512*About the job***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:*** Act as Qualified Person back-up for importing license. Ensure compliant market batch release according to local regulation* Support the CQH to ensure robust system for GxP and health-regulated activities in compliance with Sanofi standards and with applicable local regulatory requirements.* Support Quality culture & promote Quality mind-set into the country governance, working principles and ways of operating.* Support quality oversight on country local contract manufacturers, distributors and GxP service providers.* Act as contact person for local health authorities for topics linked to quality control of product in Ukraine.* Support a process for management of GxP documents and records is in place in all GxP processes, considering data integrity principles.* Support information sharing, training sessions or programs related to processes under the responsibility of country quality for concerned country associates.* Support country regulatory inspections under quality responsibility, GMP regulatory inspection on manufacturing sites, country quality audits and provide support to other GxP country functions in country regulatory inspections for processes in their respective areas of responsibilities* Support inspection readiness and continuous quality improvement.* Support quality of products is managed according to Sanofi standard and local regulation* Support quality agreements with manufacturers, distributors (internal & external).*About you** 2 years’ experience with QMS in pharmaceutical industry (distribution and re-packaging experience is advantage).* Some experience with Import license is required* Knowledge of Good Distribution/Manufacturing guidelines/legislation. Knowledge of other GxP guidelines would be an advantage.* 1 years’ experience with batch release is advantage.* University qualification: Completed higher education (master level). Degree in Pharmacy is preferred, other degrees: Chemistry, Chemical Technology and Engineering, Biotechnology and Bioengineering, Biomedical Engineering, Biology or another life science discipline.* Analytical skills, ability to communicate with internal and external stakeholders, result-oriented team player* Ukrainian and English – advanced level both oral and written* Bring the miracles of science to life alongside a supportive, future-focused team.* Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.* 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.#LI-EUR**Pursue** *Progress*. **Discover** *Extraordinary*.Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before.*Progress* and 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, gender identity, protected veteran status or other characteristics protected by law.Diversity und Inklusion sind in den Grundwerten von Sanofi verankert und spiegeln sich in unserer Arbeitsweise wider. Wir respektieren die Vielfalt unserer Belegschaft in Hinsicht auf ihre Herkunft, Erfahrungen und Lebensweisen. Wir erkennen die Bereicherung, die diese Vielfalt birgt, und fördern Inklusion sowie
eine Arbeitsumgebung, in der diese Unterschiede sich weiter entwickeln können, zur Stärkung des Lebens unserer Mitarbeiter, Patienten und Kunden. #J-18808-Ljbffr