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I’m wrapping up a series of studies that produced large LC-MS/MS and GC-MS/MS datasets and I need a fresh, expert eye on the numbers. The raw files are already organized in Chromeleon and MassLynx; what I’m missing is confident, defensible interpretation that I can drop straight into my reports. Here’s what you will walk into: • Fully integrated chromatograms with baseline and peak picks completed. • Method development and validation records prepared under GLP/GMP, so all audit trails are in place. What I need from you: • Re-examine the processed data, confirm the peak assignments, and deliver clear, concise interpretations that tie back to the method objectives. • Flag any integration anomalies that might compromise accuracy before I submit final results. • Provide short narrative comments (or a table, if cleaner) explaining each call you make so the reasoning is transparent for QA review. Acceptance criteria • Interpretations must align with current method validation parameters (specificity, linearity, accuracy, precision, LOD/LOQ). • Any recommended re-integration or re-analysis steps should cite the exact retention time window and ion transition involved. • Final deliverable: a single PDF report plus the updated Chromeleon/MassLynx sequence files, delivered within the agreed timeline. When you message me, focus on your direct experience handling both LC-MS/MS and GC-MS/MS datasets and your comfort working under GLP/GMP. A brief note about similar studies you’ve interpreted is enough—I value depth of experience over a lengthy proposal.
Project ID: 40598301
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4 freelancers are bidding on average ₹24,875 INR for this job

I'm an analytical chemist with hands-on experience interpreting LC-MS/MS and GC-MS/MS datasets under GLP/GMP conditions, including peak assignment confirmation, integration anomaly review, and audit-ready documentation in Chromeleon and MassLynx. I'll re-examine your processed data, confirm all peak assignments against your validation parameters, flag any integration issues with exact retention time windows and ion transitions cited, and deliver a clean PDF report with transparent QA-ready narrative commentary alongside your updated sequence files. I've done similar work on multi-analyte quantitation studies where defensible interpretation under regulatory scrutiny was non-negotiable. Ready to start immediately.
₹25,000 INR in 7 days
4.1
4.1

Hi, Your project is a great match for my background, and I’d be happy to help. I’m a former Bioinformatics Scientist at Columbia University with 5+ years of experience working with LC-MS/MS and GC-MS datasets, including data review, peak evaluation, quality control, method validation, and interpretation for biomedical research. I’ve worked extensively with targeted and untargeted mass spectrometry data, reviewing chromatographic performance, investigating peak quality, identifying potential integration issues, and ensuring results are accurate, reproducible, and ready for reporting. I’m also familiar with GLP/GMP-style documentation and understand the importance of providing clear, defensible analytical decisions that stand up to QA review. I can carefully review your processed data, verify peak assignments, highlight any integration concerns, and provide concise, well-documented interpretations linked to the relevant retention time windows and validation criteria. My goal is to deliver results that you can confidently include in your final report. I value clear communication, attention to detail, and timely delivery, and I’d be happy to review a sample dataset first so we can align on expectations before moving forward. I’d love the opportunity to work with you. Looking forward to hearing more about your study! Hanisha Udhani
₹24,500 INR in 5 days
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0.0

I would be happy to review and interpret your LC-MS/MS and GC-MS/MS datasets for final report preparation. I have experience in analytical chemistry, chromatographic data interpretation, method validation documentation, peak assignment review, integration anomaly checking, and GLP/GMP-style reporting. I understand the importance of aligning interpretations with validation parameters such as specificity, linearity, accuracy, precision, LOD/LOQ, retention time consistency, ion transitions, and audit-ready reasoning. I can re-examine the processed Chromeleon and MassLynx data, confirm peak assignments, flag any suspicious integrations or baseline issues, and prepare concise interpretation comments suitable for QA review. The final deliverable can include a clear PDF report with table-based observations, retention time/transition-specific recommendations, and any suggested re-integration or re-analysis steps where needed.
₹25,000 INR in 7 days
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