a
arooj_ehsan

Arooj Sultana

@arooj_ehsan

Biotechnologist and Cleanroom Technical Specialist

Pakistan
Anglais, Ourdou
Certaines informations sont présentées en anglais.
À propos de moi
I am a biotechnologist working in the medical instrument industry, with professional experience in cleanroom environmental monitoring and technical documentation. I can assist with cleanroom particle-count data analysis, trend analysis, Excel data organization, scientific and technical writing, proofreading, and biotechnology-related educational content. I provide accurate, well-organized and original work while respecting confidentiality and applicable quality requirements.... Plus d’infos

Compétences

a
arooj_ehsan
Arooj Sultana
hors ligne • 

Voir mes services

Consulting en analyse de données
I will analyze cleanroom particle data in excel
De10 $US / projetPlus de détails
Nettoyage des données
I will clean organize and analyze your excel data
De15 $US / projetPlus de détails

Portfolio

Expérience professionnelle

Goldstar_Medical Instruments

Cleanroom In-charge

Goldstar Medical Instruments • Temps plein

Sep 2025 - Present • 1 yr 1 mo

Responsible for overseeing cleanroom operations and maintaining controlled environmental conditions in a medical instrument manufacturing environment. My experience includes cleanroom monitoring, airborne particle-count analysis, environmental monitoring, documentation, and data review. I have developed practical knowledge of cleanroom classification, contamination control, particle monitoring, monitoring trends, deviation identification, and quality-focused documentation. I also work with data analysis and technical reporting to support informed quality decisions. Key knowledge and achievements: • Practical knowledge of cleanroom operations and contamination-control principles • Experience with airborne particle monitoring and trend analysis • Understanding of cleanroom environmental monitoring requirements • Ability to analyze monitoring data and identify unusual trends • Experience preparing and reviewing technical documentation and reports • Strong understanding of quality-focused practices in a medical-device manufacturing environment • Ability to organize technical data into clear Excel-based summaries and visual reports • Continuous development of knowledge in cleanroom practices, quality systems, and technical documentation