Zena Musoki
Process Engineer at Tessenderlo Group- Claim this Profile
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French Native or bilingual proficiency
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English Full professional proficiency
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German Limited working proficiency
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Dutch Elementary proficiency
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Spanish Elementary proficiency
Topline Score
Bio
Experience
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Tessenderlo Group
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Belgium
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Chemical Manufacturing
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200 - 300 Employee
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Process Engineer
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Dec 2019 - Present
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FAREVA
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Manufacturing
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700 & Above Employee
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Industrialization Project leader
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Feb 2019 - Aug 2019
Piloting industrial transfer of new comectics produts between sites- Coordination of different actors : production, suppl chain, quality, SHE- Reporting to the hierarchy and the clients- Exchanges with suppliers and supply management- Management of feasability tests- Adaptation of production tool with industrialization technicians- Scheduling and supervision of pilot trials until 1st commercial production
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Borealis
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Chemical Manufacturing
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700 & Above Employee
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Production engineer
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Sep 2018 - Dec 2018
In charge of implementing operational excellence in ammonia and water treatment plant units and operations follow-up.- Implementation of a process and Tools for alarms management (working with shift teams and automaticians).- Daily production balances and SAP entry. - Order and receipt of raw materials and SAP entry.- Participation to security turns on the site : exchanges with operators and subcontractors. - Preparation of works orders for the isolation of an unfunctional unit. - Participation in HAZOP
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Sanofi
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France
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Pharmaceutical Manufacturing
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700 & Above Employee
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Project leader Injectable medical devices
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May 2016 - Oct 2017
Responsible of the development of injectable drug-device combination products (mAbs pre-filled syringes) in Primary Packaging & Devices service.- In charge of design verification and validation (design control) and the associated documentation, in respect with plannings, for submission to the FDA.- Development, writing and validation of tests methods / protocols in collaboration with technicians and in respect with GMP.- Transverse work, as focal point, in interaction with Regulatory Affairs, Quality, Risk Management, Industrialization, QC and industrial site.- Exchanges with worldwide partners, suppliers and subcontractors.- Follow-up of deviations, CAPAs.- Management of changes (change controls).- Follow-up of stabilities in the frame of Life Cycle Management.- Preparation and participation in internal and FDA audits.
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Sanofi
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France
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Pharmaceutical Manufacturing
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700 & Above Employee
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Process development Engineer
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Mar 2015 - Sep 2015
Internship in industrial development C&BD service (Chemistry & Biotechnology Development)Production support and troubleshooting on hydrocortisone extraction process (DSP) following the starting of a biochemical production unit, for performances improvement.-Scale-down of biomass deactivation for the improvement of industrial performance in respect with environmental constraints.-Study of ways to control contamination in facilities.-Study of solutions to address clugging issues in membrane operations.-Setup of a data basis for a MVDA (multivariate data analysis) study in order to link USP parameters with DSP behaviours and have a better understanding and control of the process.
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Master thesis : Photodegradation of phenol in UV-LEC reactor
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Sep 2014 - Feb 2015
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R&D project
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Jun 2014 - Aug 2014
Synthesis and characterisation of polymeric nanoparticles for oral drug delivery.In Dr. Juan M. Irache team, in european project framework.
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Industrial placement (stage ouvrier)
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Jun 2014 - Jul 2014
Finishing line operator.With observation and evaluation of safety conditions at work.
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Education
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ENSIC (Ecole Nationale Supérieure des Industries Chimiques), Nancy
Chemical Engineer / Master degree, Process Engineering / chemical engineering -
Katholieke Universiteit Leuven
Master of Science in Chemical Engineering -
Lycée Lakanal, Sceaux
Classe préparatoire, Physics, chemistry, engineering sciences