MSAT Process Engineer Consultant

Job title:

MSAT Process Engineer Consultant

Company:

Start People

Job description

DescriptionThe Manufacturing Science and Analytical Technology department (MSAT) represents the scientific backbone of the company that provides commercial support, process/method optimization (lifecycle management), technology transfer of new products and processes/methods and development of innovative, robust, and cost-effective next-generation processes/methods.The focus of the MSAT Process Engineer Consultant is on the upstream cell culture part of the manufacturing process.Starting from thorough scientific and technical knowledge, this role will contribute to (small scale) Technology Transfer activities aiming at introduction of new products and processes at the Sanofi Geel biopharmaceutical manufacturing site. Additionally, you will contribute to improvement initiatives of existing processes at the Sanofi Geel site and within the broader Sanofi network. Your role will primarily involve laboratory-scale activities, so you should have a strong affinity for working in a lab environment.Tasks:

• Contribute to the introduction of new drug substance manufacturing processes by supporting the technology transfer of small-scale models, representing the large-scale process, from a development laboratory into the MSAT lab.
• Design and conduct lab experiments to achieve successful small-scale model transfer and generate reports of conducted experiments and a comprehensive data package for model qualification. Identify and drive small scale process improvements to increase model fit to large scale process.
• Generate scientific/technical study protocols and reports of the small-scale experiments to support investigations and assess the impact on the manufacturing process.

CompanyWe, at Sanofi, are there beside people in need, as a health journey partner+100,000 employees, representing 142 nationalities90 countries where Sanofi is present, providing healthcare solutions in 170 countries69 manufacturing sites in 32 countries

21 Research and Development sites comprising medicines, clinical research and vaccinesProfileRequirements:

• PhD or master in Life Sciences, with relevant experience of minimum 3 or 5 years respectively in process development or MSAT-like functions
• Oral and written fluency in English given the international context
• Experience in mammalian cell culture processes on lab- and/or manufacturing scale; experience with purification processes is a plus
• Enthusiastic about conducting small-scale studies in a lab environment
• Flexible, e.g. you agree to work occasional evenings/weekends
• Ability to adapt to changing priorities
• Strong communication, i.e. you connect, discuss and come to a compromise with people in other departments or sites
• Excellent analytical and problem-solving mindset, accurate with the necessary eye for detail
• Familiar with various statistical and data trending techniques, knowledge of or experience with JMP/Statistica/Matlab/Simca is a plus
• You have a GMP mindset, being familiar with current Good Manufacturing Practices is a plus

Offer

• A consultancy position through our consultancy supplier
• A full-time day shift position with flexible hours.
• The opportunity to make a difference in a varied position at local level within an international and dynamic company focused on the health and well-being of people.
• A stimulating work environment where you can further develop your talents and where there is room for personal growth.
• A competitive salary and attractive benefits.

Expected salary

Location

Geel, Anvers

Job date

Wed, 17 Jul 2024 22:33:56 GMT

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