Manufacturing and Supply
Wo Wunder
der Wissenschaft
für Patient*innen
Realität werden
Project Manager (FCS-05)
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Unsere Teams produzieren und liefern jedes Jahr über 4 Milliarden Einheiten an Medikamenten und Impfstoffen und sorgen dafür, dass jede Innovation die Menschen erreicht, die sie am dringendsten benötigen. Unsere hochmodernen Produktionsstätten, KI-gestützten Smart Factories und wegweisenden Automatisierungstechnologien setzen neue Maßstäbe – damit Behandlungen Patient*innen schneller, sicherer und nachhaltiger als je zuvor erreichen. Hier kannst Du mit Deinen Fähigkeiten, Deinen Ambitionen und Deiner Leidenschaft die Zukunft des Gesundheitswesens mitgestalten.
Job title: Project Manager (FCS-05)
- Location: Csanyikvölgy, Miskolc
- Hiring Manager: Zoltán Kozári
- Job Type: Indefinite, full-time
About the job
The Project Manager is responsible for directing the project and ensuring timely completion within the budget, installing a solution that meets user requirements and is accepted and understood by users. They lead planning and implementation, ensuring compliance with conditions in cooperation with Sanofi Group DP, OSD & Pack Technical division and CSA site management.
Lead and manage an end-to-end installation project of plastic free pharmaceutical packaging machines at SANOFI CSANYIK site, ensuring compliance with GMP standards, regulatory requirements, and customer specifications. This role is critical for delivering high-quality, validated packaging solutions for pharmaceutical products.
Key Responsibilities
Monitor project budget, timeline and risks (responsible for escalation to local, regional, and global program management in case of any budget issues).
Develop a detailed project organization and plan.
Define user requirements in collaboration with key users and ensure they are met.
Track project progress (prepare regular progress plans as requested and reports).
Manage project team, processes and tasks.
Ensure collaboration and communication necessary for project execution.
Handle documentation needs and documents required for project implementation.
Responsible during the project for:
Creating and approving user specifications.
Supporting tender processes for project manufacturing machines/equipment.
Approving and supporting tests, qualifications, validations, and related documents for project machines/equipment.
Overseeing installation and commissioning of project machines/equipment at the site.
Summarize and provide feedback on project lessons learned.
1. Project Planning & Preparation
Develop and manage comprehensive project plans including timelines, resource allocation, and budget forecasts.
Coordinate pre-installation activities such as site readiness checks, utility requirements, and cleanroom compliance.
Organize FAT (Factory Acceptance Test) and ensure all documentation is complete before shipment.
2. Installation & SAT
Supervise mechanical and electrical installation of plastic free packaging machines and associated equipment.
Ensure proper integration with upstream/downstream systems (e.g., blister machines, cartoners, serialization units).
Lead SAT (Site Acceptance Test) and ensure successful commissioning according to GMP standards.
3. Validation & Compliance
Manage IQ/OQ/PQ qualification processes in collaboration with Quality Assurance teams.
Ensure all activities comply with pharmaceutical regulations and customer-specific SOPs.
Maintain accurate and complete documentation for audits and regulatory inspections.
4. Technical Leadership
Provide technical guidance to installation teams and troubleshoot complex issues during setup. Manage installation team.
Coordinate with automation engineers and ITS for software configuration and system connectivity.
Ensure machine performance meets specifications for speed, accuracy, and product integrity.
5. Stakeholder Communication
Act as the primary point of contact for customers throughout the project lifecycle.
Conduct regular progress meetings and provide transparent status reports to internal stakeholders.
Manage expectations and resolve conflicts related to timelines, scope, or technical challenges or manpower needs.
Ensure proper cooperation among site project team members and stakeholders outside the site. Coordinate collaboration between site and external project members. Share information with colleagues and strive to maintain a productive work environment.
6. HSSE, Risk & Issue Management
Early identify potential risks (technical, regulatory, logistical) and develop mitigation strategies.
Respond promptly to installation delays or equipment malfunctions to minimize downtime.
·Health, Safety, Security, Environment:
Comply with occupational safety, fire safety, environmental protection, and asset protection rules and regulations. Warn colleagues and immediately report hazardous situations to superiors to reduce risk.
Regularly check personal protective equipment before starting work and use it properly. In case of malfunction, error, or unexpected situation, warn colleagues, act as expected to resolve it, or report to a superior. Report accidents or near misses immediately.
7. Training & Handover
Plan to organize operator and maintenance training sessions for staff jointly with assigned team leads.
Ensure the preparation of a detailed handover documentation; make sure to include SOPs, maintenance schedules, and troubleshooting guides by vendor.
·
Documentation:
Prepare and support project-related documentation according to regulations.
GMP (Good Manufacturing Practice)
Attend mandatory GMP training and acquire the necessary knowledge. Perform work according to valid quality assurance and GMP rules and procedures.
About You
Several years of significant experience in a Project Manager roles. Project management skills and knowledge.
Ensure the preparation of a detailed handover documentation; make sure to include SOPs, maintenance schedules, and troubleshooting guides by vendor.
Sticking to timelines and deadlines, Ability to manage multiple projects streams under strict timelines.
High affinity for using digital/IT tools.
Advantages:
Knowledge of GMP.
5+ years in preferably multinational pharmaceutical packaging machinery installation and 5 years in manufacturing project management.
Hands-on experience with plastic free packaging systems or similar modular packaging solutions.
GMP training highly desirable.
Knowledge of pharmaceutical packaging processes, serialization, and track & trace systems.
Familiarity with validation protocols (IQ/OQ/PQ) and regulatory compliance.
Technical Competencies:
Strong communication and collaboration skills. Situational leadership.
Good and fast decision-making and problem-solving ability.
Creativity and innovation.
High sense of urgency and sense of responsibility.
Commitment to continuous process improvement.
Ability and skills to properly communicate in English (with focus on project management).
MS Office proficiency.
Additional Requirements:
Willingness to travel occasionally (internationally)
Proficiency in project management tools (MS Project, SAP) and technical documentation.
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.
Why choose us?
· Join a leading pharmaceutical company and contribute to improving health outcomes worldwide.
· Be part of a company at the forefront of medical research and breakthrough therapies.
· Thrive in an environment that values diversity of thought and background.
· Work closely with global and local teams, gaining exposure to various aspects of the pharmaceutical business.
#LI-EUR
nullPursue Progress. Discovery Extraordinary.
Werde Teil von Sanofi und starte mit uns in eine neue Ära der Wissenschaft – wo dein persönliches Wachstum genauso wegweisend ist wie unsere Arbeit. Wir investieren in dich, damit du weiterkommst, schneller denkst und Dinge möglich machst, die vorher undenkbar waren. Du wirst Grenzen verschieben, Gewohntes hinterfragen und smarte Lösungen entwickeln, die direkt bei den Menschen ankommen, für die wir da sind. Bereit, die Wunder der Wissenschaft zu jagen und Leben zu verbessern? Dann lass uns gemeinsam Großes bewegen – und das Außergewöhnliche entdecken.
Bei Sanofi stehen allen die gleichen Chancen offen – unabhängig von Herkunft, Hautfarbe, Religion, Geschlecht, Nationalität, sexueller Orientierung, Alter, Staatsangehörigkeit, Familienstand, Behinderung, Geschlechtsidentität, Veteranenstatus oder anderen gesetzlich geschützten Merkmalen.
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Warum bei uns arbeiten?
- Wir stellen nicht nur Medikamente her – wir bewirken etwas. Unser globales Netzwerk modernster Produktionsstätten sorgt dafür, dass Patient*innen die Behandlungen erhalten, die sie brauchen – genau zur richtigen Zeit.
- Innovation treibt uns an. Von KI-gestützter Fertigung bis hin zu weltweit führenden Produktionsmethoden setzen wir neue Maßstäbe in Effizienz und Leistung.
- Hier wachsen Karrieren. Ob in der Produktion, Qualitätssicherung, Ingenieurtechnik oder in der Supply Chain– arbeitest Du mit erstklassigen Talenten zusammen, entwickelst Deine Fähigkeiten weiter und gestaltest die Zukunft der Pharmaindustrie mit.
- Wir tun, was richtig ist. Sicherheit, Nachhaltigkeit, Vielfalt, Gleichberechtigung und Inklusion stehen im Mittelpunkt unseres Handelns – für ein Arbeitsumfeld, in dem alle erfolgreich sein können.
All-In für Vielfalt
Bei Sanofi führen unterschiedliche Perspektiven zu den besten Lösungen für Patient*innen. Erfahre von Monique Vessey, unserer Leiterin der Supply Chain -Transformation, wie ihre persönliche Geschichte ihre Arbeit bei der Bereitstellung lebenswichtiger Medikamente prägt.
"Manufacturing & Supply bildet die Brücke zwischen der Wissenschaft in unseren Forschungslaboren und den Menschen und Gemeinschaften, die wir versorgen."
Brendan O’Callaghan
Executive Vice President of Manufacturing and Supply
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