Proactively seek out ways to improve individual and team-wide scientific processes and operations.Onboard new staff to the lab, including training in standard operating procedures, equipment-specific requirements, and ordering.Quality assurance assisstance:Management and preparation of the laboratory to work under GLP standards.Writing of procedures, protocols, and working templates - Manuals, SOPs, and Working instructions.Study director:Developmental NeuroToxicity (DNT) testing project management, as part of an international consortium. IATA Case Study coordinated by OECD.

Laboratory designer and LIMS manager:Structure new spaces as work areas, in a changing environment of both equipments and staff. Develop LIMS implementation, configuration and maintenance of it.Product management:Procurement and maintenance of supplies, chemicals, and biological inventories - ensure that consumables, buffers, reagents, samples are stocked, created, and shipped as needed.Collecting, receiving, labeling, and storing samples or reagents.Management of the lab ordering system - including placing orders, tracking of shipments.Equipment management:Including cataloging, surveillance, routine maintenance, and lead to ensure any required equipment repair.Develop and implement quality assurance programs for maintenance and calibration of equipment.Act as point of contact for Health and Safety Department.

Performe laboratory-based scientific investigations by carrying out routine technical tasks and experiments. Use of zebrafish larvae (Danio rerio) for screenings of novel chemical molecules.- Organotoxicity assays: Acute toxicity, teratogenicity, cardio-, neuro- and hepato-toxicity.- Efficacy assays: Neuro- and cardio-protection.- Genotyping of genetically modified larvaes and gene expression assays.- Validation project assistance.

Protein purification processes in manufacturing departement under GMP standards.Shift manager.Co-work with QA, QC and Technical service departments.Scale-up procedure design for a tech-transfer project.

My first industrial experience was at a Biopharmaceutical company. I began working in Downstream Process Development Department on Characterization and Validation Processes. At the end of the project, I was relocated to Downstream Manufacturing Department.· Proteins purification process.· Work under GMP environment.· Scale-Down Characterization and Optimization Processes.· Chromatographic techniques: TLC, RP-HPLC, FPLC (Akta Avant, Pilot, Ready, Process): affinity, ion exchange, hydrophobic, gel filtration, protein A· Solubilization and refolding of proteins. · Protein concentration and diafiltration by tangential filtration (TFF). · Virus removal by nanofiltration.

Co-create a solution as a member of an interdisciplinary team:-Facilitate the monitoring of the work of research groups.-Develop a systematic assessment of the groups.

Freshwater (Chlorella vulgarius) and saline (Nannochloropsis) micro-algae growth and study. Its immobilization to magnetic nanoparticles for biotechnology use.

Support for the preparation of university entrance examination.

I have gained valuable experience in the field of Biochemistry research acquired in the Master's thesis andfollowing months that I continued working in the lab. In the enzymatic technology group, I learned tosynthesize paramagnetic nanoparticles and immobilize them to protein and microalgae.· Biodiesel scaled up production catalyzed by magnetic cross-linked enzyme aggregate (mCLEAs).· Synthesis and functionalization of magnetic CLEAs of commercial lipases. · Second-generation biodiesel. Biofuels production from nonfood crops and waste cooking oil.