Biyoteknoloji Jobs

## **Project Title** **BIRAC BIG Grant Application – Proposal Writing & Technical Expert Required** ## **Project Description** We are a healthcare-focused deep-tech startup preparing our application for the **BIRAC Biotechnology Ignition Grant (BIG)**. We are seeking an experienced freelancer/consultant with **prior hands-on experience in BIRAC BIG or other BIRAC/DBT grant applications** to support us in drafting and refining a **submission-ready proposal**. The freelancer will work closely with the founder to structure the application in line with **BIRAC evaluation criteria**, ensuring scientific accuracy, feasibility, regulatory alignment, and strong commercialization logic. --- ## **Scope of Work** 1. **Innovation & Problem Understanding** * Understand the core i...

I need an experienced biochemist to help me create a brand-new, small-scale purification workflow for monoclonal IgG isolated directly from human plasma or serum. The objective is not to follow a routine protocol but to design, test, and document a method that improves yield, purity, or turnaround time over existing approaches. What I bring: • Access to screened human plasma/serum samples and basic downstream analytics (SDS-PAGE, ELISA, UV-Vis). • Laboratory space equipped for column chromatography and standard buffer preparation. What I count on you for: • Critical review of current monoclonal IgG purification literature and identification of process gaps. • Step-by-step experimental design tailored to my lab’s equipment, including detailed buffer composi...

I need a publish-ready narrative review that examines how the latest genomic technologies are reshaping cancer research, with a sharp eye on where the knowledge still falls short. Rather than cataloguing every study, the manuscript should weave together key findings—next-generation sequencing, single-cell analyses, CRISPR screens, long-read platforms—and critique the blind spots these tools reveal (or sometimes create) across tumour biology, diagnosis and therapy development. The central thread must be highlighting the unanswered questions and methodological limitations that deserve future funding and lab time. Scope • Roughly 5,000–7,000 words, written for a high-impact oncology journal. • Current primary literature only (2018-2024 preferred) sourced from ...

I am preparing to sell research-grade peptides and related bioregulators and need solid, practical guidance to ensure full compliance with regulations worldwide. My key focus is regulatory compliance; I am not looking for contract drafting or IP work at this stage. What I need from you • A clear map of the governing bodies that regulate peptides in the United States (FDA, DEA, state boards), European Union (EMA, customs), Australia (TGA, customs) and any other major markets we identify together. • An analysis of how these agencies currently classify peptides and bioregulators, including the grey areas that often trigger enforcement. • Step-by-step guidance on what I can legally say on my website, labels and marketing materials, plus any required disclaimers for a &ldquo...

I am preparing to sell research-grade peptides and related bioregulators and need solid, practical guidance to ensure full compliance with regulations worldwide. My key focus is regulatory compliance; I am not looking for contract drafting or IP work at this stage. What I need from you • A clear map of the governing bodies that regulate peptides in the United States (FDA, DEA, state boards), European Union (EMA, customs), Australia (TGA, customs) and any other major markets we identify together. • An analysis of how these agencies currently classify peptides and bioregulators, including the grey areas that often trigger enforcement. • Step-by-step guidance on what I can legally say on my website, labels and marketing materials, plus any required disclaimers for a &ldquo...

I am preparing to sell research-grade peptides and related bioregulators and need solid, practical guidance to ensure full compliance with regulations worldwide. My key focus is regulatory compliance; I am not looking for contract drafting or IP work at this stage. What I need from you • A clear map of the governing bodies that regulate peptides in the United States (FDA, DEA, state boards), European Union (EMA, customs), Australia (TGA, customs) and any other major markets we identify together. • An analysis of how these agencies currently classify peptides and bioregulators, including the grey areas that often trigger enforcement. • Step-by-step guidance on what I can legally say on my website, labels and marketing materials, plus any required disclaimers for a &ldquo...