Network VC is a syndicate venture fund and platform for a decentralized ecosystem of independent VC professionals that invests in early stage startups across global geographies. Network VC invests in 2-4 startups per month. We invest in technology startups at Seed to Series A stages. We invest from $100k to $500k check sizes and have LPs from 20 countries. We co-invested together with Softbank, Andreessen Horowitz, Founders Fund, Khosla Ventures, General Catalyst etc.

-Offered comprehensive guidance and solutions to assist venture-backed biotech innovators in transforming their ideas from concept to consumer, driving momentum to market.-Managed contracts and budgets with annual revenue up to $10M.-Responsible for project delivery, profit & loss accountability, and customer satisfaction through management of program and projects.

Actively sourcing, conducting due diligence, and pitching startup deal flow to GoingVC Partners, the funding vehicle of GoingVC.

- Project lead for verification and validation of Oncoguard Liver assay through execution and planning of analytical validations, material procurement, risk management, and technical problem resolution.- Evaluation, testing, and validation of secondary sources vendor materials used in lab automation workflows.- Lead in design transfer of lab instrumentation and processes for installation and validation of international lab deployment.- Integration of internal laboratory processes… Show more - Project lead for verification and validation of Oncoguard Liver assay through execution and planning of analytical validations, material procurement, risk management, and technical problem resolution.- Evaluation, testing, and validation of secondary sources vendor materials used in lab automation workflows.- Lead in design transfer of lab instrumentation and processes for installation and validation of international lab deployment.- Integration of internal laboratory processes, LIMS, external stakeholders in system validation planning and execution. Show less

-Design and architecture of LUNAR-2 assay platform using flowcharts to characterize system interactions between software, lab automation, data pipeline, and LIMS.- Standardize usage of requirements management tools for design testing, requirements management, risk management, and document generation.- Testing, design, development of assay automation system.- Decomposition of user requirements to create subsystem specifications.

- System development of Singulex Clarity System for cardiac troponin (cTnI), thyroid stimulating hormone (TSH), and clostridium difficile (C. diff.) assays- Successful submissions of Singulex Clarity System and cardiac troponin assay for CE mark and FDA approvals.- Led in design, development, and verification of liquid handling parameters for various assay processes.- Interfacing between stakeholders to gather, manage, and document product requirements and attain requirements… Show more - System development of Singulex Clarity System for cardiac troponin (cTnI), thyroid stimulating hormone (TSH), and clostridium difficile (C. diff.) assays- Successful submissions of Singulex Clarity System and cardiac troponin assay for CE mark and FDA approvals.- Led in design, development, and verification of liquid handling parameters for various assay processes.- Interfacing between stakeholders to gather, manage, and document product requirements and attain requirements acceptance.- Authored, planned, and executed complex system wide test activities on automated test system platform.- Systems support and troubleshooting on technical issues in LIMS, Tecan hardware components.- Risk management, FMEA, hazard analysis activities in regards to system workflows.- Programmed scripts/processes/methods in EVOware software for development and production applications.- Supported external customer sites by providing hands-on support on installations, instrument usage, maintenance, and designated user workflows. Show less

- System development and design verification/validation activities for the cobas s201 system, p 512, p 612, cobas 4800 platforms, which have undergone successful regulatory submissions.- Feasibility and ad-hoc/debug testing of lab automation processes, software workflows, customer workflows.- FMEAs, CAPAs to identify, recognize, and evaluate process failures.- Create technical documents pertaining to design history, design, control, test protocols, SOPs, and summary reports for… Show more - System development and design verification/validation activities for the cobas s201 system, p 512, p 612, cobas 4800 platforms, which have undergone successful regulatory submissions.- Feasibility and ad-hoc/debug testing of lab automation processes, software workflows, customer workflows.- FMEAs, CAPAs to identify, recognize, and evaluate process failures.- Create technical documents pertaining to design history, design, control, test protocols, SOPs, and summary reports for regulatory submission.- Usability engineering in accordance to ISO 62366- IQ/OQ/PQ development and deployment. Show less

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