Biotechnology Jobs

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...

Je cherche un spécialiste capable de réaliser une électrophorèse sur gel de polyacrylamide (PAGE) afin de vérifier l’intégrité de mes échantillons de protéines. Les échantillons sont déjà préparés et expédiés sous glace sèche ; je fournis la composition des tampons recommandés. Ce que j’attends : • Exécution d’une PAGE adaptée (réductrice ou native selon vos recommandations) • Numérisation haute résolution du gel et transfert des images brutes (.tiff ou .png) • Rapport succinct interprétant les bandes : présence d’agrégats, pureté, éventuelles d&ea...