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annajamesq

Anna J

@annajamesq

GMP Compliance Support

Verenigd Koninkrijk
Spaans, Frans, Nederlands
Sommige informatie wordt in het Engels weergegeven.
Over mij
Hello, I’m Anna James. I’m detail oriented, organized, and passionate about quality, structure, and doing things the right way. I enjoy helping people bring clarity to complex work and turning messy information into clear, reliable results. I value professionalism, communication, and delivering work people can trust. When I take on a project, I treat it with responsibility and care from start to finish. Outside of work, I enjoy learning new skills and continuously improving myself.... Lees meer

Skills

a
annajamesq
Anna J
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Gemiddelde reactietijd: 1 uur

Bekijk mijn diensten

Technische teksten
I will create professional gmp sop for pharma or medical devices
Technische teksten
I will prepare you for gmp or fda inspection with mock audit questions

Portfolio

Werkervaring

Fiverr

GMP / Regulatory Compliance Sop Writer

Fiverr • Freelance

Mar 2024 - Present2 yrs 5 mos

Author Standard Operating Procedures (SOPs) and regulatory compliance documentation for pharmaceutical and life sciences processes, including GMP frameworks aligned with 21 CFR Part 210/211 requirements. Developed a comprehensive SOP establishing a Pre-Approval Inspection (PAI) readiness framework for New Product Introduction (NPI), covering cross-functional responsibilities, RACI matrices, phase-based process workflows, and inspection preparation timelines. Skilled in translating complex regulatory requirements into clear, structured, audit-ready documentation including guiding principles for data integrity, risk-based inspection preparation, and coordination with external manufacturing and testing partners (CMOs/CTLs). Experienced in supporting quality assurance teams with documentation that withstands regulatory scrutiny and mock inspection review.