Help the refugees

If you move around the world by choice, consider helping those forced from their homes by conflict. Donate to the UN Refugee Agency today.

Back

Cadre de développement des procédés de purification H/F

Visit website

Sanofi Vitry-sur-Seine est l’un des sites les plus innovants du Groupe, avec plus de 2 000 collaborateurs.​

Doté d’un outil de production ultramoderne, le Biolaunch, le site maitrise à la fois les activités de recherche, de développement et de fabrication de produits de biotechnologies.​

Les pathologies que nous traitons ? Le cancer, les maladies neurodégénératives et les maladies cardiovasculaires.​

Le contenu du poste est libellé en anglais car il nécessite de nombreuses interactions avec nos filiales à l’international, l’anglais étant la langue de travail.

DEPARTMENT DESCRIPTION

The Global Manufacturing Sciences and Technology (MSAT) is a center of excellence in manufacturing and process sciences and as such is the keeper of the body of manufacturing process knowledge. It is a multi-disciplinary function that provides expertise in process and analytical sciences; manufacturing sciences, process modelling, trending and statistical analysis; process validation and technology transfer.

The Global MSAT organization is the seeding ground for technical and scientific talent that executes their work in matrix organization. Furthermore, the Global MSAT is providing cross-functional training and development and is the portal for collaboration with many different organizations including process development and operations.

In that scope, Global MSAT is responsible for

  • Providing on-the-floor technical and scientific support
  • Providing expertise in process/product-related investigations
  • Overseeing and leading data management, monitoring and statistical analysis
  • Owning technical transfers and process validation
  • Defining and maintaining the product control strategy
  • Owning comparability and product characterization
  • Identifying commercial process/product life cycle improvements
  • Identifying and driving implementation of improvements to maximize throughput and capacity utilization

Within the Vitry-sur-Seine local Manufacturing Sciences and Technology (MSAT) organization, we are looking for an experienced Downstream Process Engineer to join our expanding team.

KEY RESPONSIBILITIES

  • Manages process fit-gap assessment in tech transfer team for purification, formulation and filling processes and identify areas requiring mitigation via process adaptation or facility modification
  • Leads process validation including strategy definition, the execution follow-up and documentation management
  • Defines and maintains the process control strategy for DSP
  • Routinely monitors DSP manufacturing process and identify trends and resolves using her/his expertise and site resources, where possible, or escalate to MSAT governing body requiring additional expertise and resources
  • Leads DSP process related complex problem investigation at the site by using solid process understanding and use of scientific and engineering principles and practices and facilitates generation of practical solutions
  • As a downstream processing SME, provides technical support during health authority inspection
  • Drives continuous process robustness and improvement in order to make processes more cost effective at the same time maintaining quality and HSE requirements
  • Develops connection within global MSAT in international context

Basic Qualifications

  • Master’s Degree or PhD in engineering or science with minimum 5 years of experience in cGMP manufacturing environment or biologics process development

Referred qualifications

  • Strong experience in process development, process characterization, technology transfer and process validation in bio-manufacture industry (8-10 years)
  • Knowledge of purification technologies and operations
  • Knowledge of viral clearance of purification processes
  • Experience with automated protein purification chromatography and UF/DF
  • Experience with DeltaV Process Control system
  • Experience in cGMP and good understanding of regulatory requirements for biologics manufacturing
  • Strong knowledge in data management and statistical analysis
  • Proficiency with MS Office (Excel, Power Point, Word)
  • Ability to make a significant contribution to cross-functional project teams through technical expertise and scientific creativity
  • Team player, ability to work effectively in a highly collaborative and dynamic environment
  • Excellent communication skills
  • Fluent in French and English

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

Summary

  • Location: Vitry-sur-Seine
  • Type: Full time
Apply now