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Azeem
@azeemakram90
Pharmaceutical QA and ISO Documentation Specialist
Pakistán
Inglés, Urdu
Sobre mí
I hold a BS (Hons.) in Chemistry with professional experience in Quality Assurance, GMP documentation, and ISO management systems. I provide documentation and compliance support for ISO 9001, ISO 14001, ISO 45001, ISO 17025, and ISO 15189 systems. I also specialize in GMP SOP writing, pharmaceutical QA documentation, validation and qualification documents, CAPA, deviation, and change control systems. My focus is to deliver practical, professional, and compliance-oriented documentation solutions.
Habilidades
Azeem
desconectado •
Tiempo medio de respuesta: 1 hora
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Escritura técnica
I will iwill write gmp sops pharmaceutical QA and iso documentation
Experiencia laboral
Quality Assurance
Pharmacists United for Truth and Transparency • Tiempo completo
Aug 2025 - Present • 9 mos
Quality Assurance professional with 7 years of experience in pharmaceutical manufacturing, GMP compliance, and documentation systems. Experienced in SOP preparation, validation and qualification documentation, CAPA, deviation handling, change control management, document control, and QA compliance activities. Trained in Quality Management System (QMS), Integrated Management System (IMS), CAPA Management, Deviation Management, Change Control System, Environmental Health & Safety (EHS), and Laboratory Management Systems. Practical exposure to implementation support and documentation requirements for ISO 9001, ISO 14001, ISO 45001, ISO 17025, and ISO 15189 standards. Skilled in preparing professional QA/QC documents, forms, checklists, logbooks, and compliance-oriented documentation for pharmaceutical and industrial environments. Focused on delivering practical, organized, and professionally structured documentation solutions according to industry standards and compliance requirements.
