Société : Start People Lieu : Geel Flanders Site source : Talent BE
The function is responsible for analytical technology transfer activities.
Our expansive portfolio covers 17 products, 5 modalities, and 3 expression systems within 12 internal and external global sites in the US and EU.
We will be supporting the launch of 20 new products in the next 5 years including monoclonal and multi-specific antibodies, fusion proteins, antibody-drug conjugate, synthorins, and nanobodies.
In recent years we have successfully established second-generation manufacturing processes with a continuous process platform.
We are pursuing future innovations such as digital labs, factory of future and advanced analytics-based process understanding and control.
In the Analytical MSAT function, we have opportunities for an MSAT Scientist who will have the following main responsibilities:
Support designing/developing/improving/validating existing analytical methods in function of existing or new production processes Independently set-up experiments and develop and carry out studies in Cell & Biochemistry-oriented teams Provide documentation through generation of scientific/technical study protocols and reports Maintain, adjust, and communicate documentation and knowledge.
Data trending and monitoring of ongoing methods, experiments, and analyses to ensure reliability, as well as have an accurate understanding of the effectiveness and efficiency of the methods Company We, at Sanofi , are there beside people in need, as a health journey partner +100,000 employees, representing 142 nationalities 90 countries where Sanofi is present, providing healthcare solutions in 170 countries 69 manufacturing sites in 32 countries 21 Research and Development sites comprising medicines, clinical research and vaccines Profile You obtained, preferably, a PhD in Life Sciences or are equivalent through experience.
You have a very good knowledge of English, both written and oral.
you are an expert in binding assays, capillary electrophoresis, spectrophotometric, plate based assays (ELISAs) etc.
and driven to execute assays in the lab.
You have excellent problem-solving skills (escalate where needed) and can handle multiple (practical) tasks at the same time.
You have good technical writing skills and are able to prepare protocols and reports.
You are accurate, result-oriented, and able to critically analyze data, draw scientifically sound conclusions, and formulate them correctly.
You have an excellent knowledge of cGMP and can convert legal requirements regarding analytical methods into effective action plans.
You are a team player and have good communication skills.
You are flexible, stress-resistant, open to change & innovation, and used to working within deadlines.
You can independently draw up a plan for projects you need to support.
Offer A position on a consultancy basis A full-time position in day shift with flexible hours.
The opportunity to make a difference in a varied position at a local level within an international and dynamic company focused on people's health and well-being.
A stimulating work environment in which you can further develop your talents and where there is room for personal growth.
A competitive salary and attractive working conditions.
