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Jyotsna Salijamula

@jyotsnasalijamula

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I maintain audit-ready quality documentation, SOPs, and controlled records in regulated environments.

United States

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What I'm looking for

I'm looking to contribute to quality documentation, document control, audit readiness, SOP management, CAPA tracking, and process improvement in a regulated environment.

At FreshRealm, I maintain quality documentation systems for regulated manufacturing, including SOPs, work instructions, batch records, quality logs, and compliance forms.

I manage 200+ controlled records with full audit-trail integrity and achieved zero documentation errors across reviewed records. I also supported three internal audits and one regulatory inspection with zero critical findings.

I investigate 30+ monthly quality issues, document deviations and corrective actions, and track CAPA closure to reduce recurrence by 25%. I work closely with Operations, Procurement, and Management to communicate quality findings and keep supplier and training records audit-ready.

Previously at Task Impetus, I managed documentation for 50+ analytical and manufacturing runs in ELN and LIMS systems with zero data integrity findings. My M.S. in Bioengineering supports my documentation, compliance, and process-standardization work.

Experience

Work history, roles, and key accomplishments

Current

Quality & Food Safety Specialist

Current

FreshRealm

Sep 2025 - Present (1 year)

Manage quality documentation systems, author and version-control SOPs, and maintain 200+ controlled records with zero documentation errors. Support compliance audits, investigate non-conformances, and track CAPA closure reducing recurrence by 25%.

Document Control SOP Development Version Control Audit Readiness CAPA Root Cause Analysis Quality Metrics Supplier Documentation Training Records Excel Microsoft Word Outlook PowerPoint

Bioprocess Engineer

Task Impetus Inc.

Apr 2025 - Sep 2025 (5 months)

Managed documentation for 50+ analytical and manufacturing runs, including SOPs, validation protocols, and batch records, with zero data integrity findings. Authored and revised quality documentation and coordinated cross-functional documentation activities.

Document Control SOP Development ELN LIMS Deviation Management CAPA Cross functional Coordination Microsoft Office

Graduate Researcher

Stevens Institute of Technology

Jan 2023 - Jan 2025 (2 years)

Maintained research documentation and controlled records under GMP-like and ISO 10993 conditions, authoring technical reports and protocol updates. Achieved 25% improvement in process outcomes through systematic documentation and standardization.

Documentation Data Analysis Microsoft Office ISO 10993 GMP Process Improvement