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ranjana sudamala

@ranjanasudamala

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Drug Safety and technical documentation professional focused on high-quality regulatory content.

India

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What I'm looking for

I’m seeking to leverage my technical communication and pharmacovigilance experience to produce high-quality regulatory and medical documentation, ensuring accuracy, compliance, and clear scientific narratives in a collaborative team environment.

I’m a detail-oriented M.Pharmacy graduate with experience in content writing and product support in the laboratory and medical equipment sector. I’m certified in Pharmacovigilance and have hands-on experience using the Argus Safety database.

In drug safety roles, I’ve worked on ICSR processing from triaging up to Medical Review, with accurate assessment of events for SmPC, CDS, IB, and PIL. I also support case processing, MedDRA coding, and adherence to global pharmacovigilance practices.

I bring strong scientific documentation skills—literature review, narrative writing, proofreading, and reference formatting—to ensure data accuracy and regulatory compliance. I enjoy collaborating across teams and taking ownership to guide content development when needed.

Experience

Work history, roles, and key accomplishments

Product Specialist-Content Writer

Labtron Equipment Ltd

Oct 2021 - Apr 2023 (1 year 6 months)

Sourced, created, and edited scientific and technical content for the laboratory and medical equipment sector, ensuring consistency in style, terminology, and formatting. Coordinated with marketing and design teams and led proofreading to ensure accuracy and adherence to editorial and regulatory requirements.

Scientific Content Writing Technical Documentation Editing and Proofreading Academic Content Development Regulatory Compliance

Trainee Scientist-Analytical Division

Vimta Labs Ltd

Dec 2015 - Aug 2016 (8 months)

Performed quality control testing of pharmaceutical samples using validated or transfer methods. Prepared validation and verification reports, protocols, and supported GMP/GLP-compliant regulatory documentation, including leachable and extractable studies.

Quality Testing Validated Methods Verification Protocols GMP GLP Regulatory Documentation

Drug Safety Process Associate

Vigi Medsafe Pvt Ltd

Supported pharmacovigilance case processing using Argus Safety and AERS databases, including triaging through medical review. Wrote clear narratives and assessed adverse event information against SmPC, CDS, IB, and PIL references.

Pharmacovigilance Oracle AERS ICSR Processing Triage Adverse Event Reporting Narrative Writing CDS