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moni_mahmuda

Moni Mahmuda

@moni_mahmuda

I will be your virtual assistant for Pharmaceutical Industry

Bangladesh
Inglés, Bengalí
Parte de la información aparece en idioma inglés.
Sobre mí
What if your business had a Virtual Assistant who thought like an Operations Partner? I am Mahmuda Moni Quality Control expert in Pharmaceutical Industry with over 8 years of experience. I offer support in preparing professional, regulatory compliant documentation. - GMP documentation (e.g. Standard Operating Procedure, Control Procedure) - Pharmacopeial Compliance (Surveillance, Impact assessment, Implementation) - Validation Protocol & Reports (Process Validation, Cleaning Validation, Analytical method validation) - Regulatory compliance - personnel training and development... Lee más

Habilidades

m
moni_mahmuda
Moni Mahmuda
desconectado • 

Revisa mis servicios

Escritura técnica
I will prepare standard operating procedures
DeUSD 50 / proyectoMás información
Asistencia general
I will manage pharmacopeial compliance for your organization
DeUSD 10 / proyectoMás información

Experiencia laboral

Nevian_Lifescience PLC

Sr. Executive, Quality Control

Nevian Lifescience PLC • Tiempo completo

Aug 2025 - Present • 1 yr

Analytical method validation/verification, process validation, cleaning validation, analytical method transfer, pharmacopeial compliance, certified GMP trainer, elemental impurity assessment, personnel training and development, Data integrity, Regulatory compliance

Novartis

Novartis

Tiempo completo • 3 yrs 4 mos

Sr. Executive, Quality Control

Mar 2025 - Jul 2025 • 4 mos

Analytical method validation/verification, process validation, cleaning validation, analytical method transfer, pharmacopeial compliance, certified GMP trainer, elemental impurity assessment, personnel training and development, Data integrity

Executive, Quality Control

Feb 2022 - Feb 2025 • 3 yrs

Raw material analysis, source development, chemical management, SOP preparation, Master control procedure preparation, Analytical method validation/verification, process validation, cleaning validation, analytical method transfer, pharmacopeial compliance, certified GMP trainer, elemental impurity assessment, personnel training and development, Data integrity