Hire the Best Biotechnology Specialists

I am a biomedical researcher and scientific consultant with 7+ years of experience in infectious diseases, public health and biology. I have contributed to international projects, including collaborations with the Centers for Disease Control and Prevention (CDC), and specialize in scientific writing, research support, and data analysis (R). I can support you with: - Scientific writing and editing - Literature reviews - Data analysis - Public health documentation - Improving your understanding in biology matters (teacher) Reliable, detail-oriented, and committed to delivering high-quality work on time.

I am a scientific consultant with an M.S. in Molecular & Cell Biology and more than 14 years of experience supporting biomedical research, scientific operations, technical writing, and evidence-based content development. My research background includes molecular biology, virology, antiviral drug screening, cell culture, transfection, reporter assays, Western blotting, ELISA, immunofluorescence, and primary cell culture. I previously worked at Boston University’s National Emerging Infectious Diseases Laboratories (NEIDL), where I supported research programs focused on high-consequence viral pathogens and laboratory operations. I am also a published scientist and co-first author on peer-reviewed research publications, including development of an Ebola virus minigenome system used for antiviral drug screening. My consulting work focuses on translating complex scientific information into clear, accurate, and evidence-based deliverables for research organizations, healthcare companies, biotechnology firms, educational platforms, and AI developers. Areas of expertise include: • Scientific literature reviews and evidence assessment • Scientific and medical writing • Systematic reviews and research synthesis • Manuscript development and publication support • Regulatory and compliance-focused scientific content • Dietary supplement and wellness content review • Technical editing and fact-checking • Clinical research documentation and study support • AI training, evaluation, and scientific content auditing • Grant, proposal, and report development Technical expertise includes: • Molecular biology and virology • PCR, RT-PCR, cloning, transfection • Western blotting, ELISA, immunofluorescence • Mammalian and primary cell culture • Experimental design and data interpretation • Scientific communication and publication development • Research operations and laboratory management Whether you need a scientific manuscript refined, a literature review conducted, regulatory-conscious content developed, or complex biological concepts translated into clear and accurate language, I bring both hands-on research experience and strong scientific communication skills to every project. Let’s discuss how I can support your project!

I'm a biochemical engineer who builds reactive HTML modelling calculators that tell food, supplement, cosmetic, and botanical founders what their next decision should actually be, instead of what a spreadsheet someone else built says it should be. Ten years as a free agent. 200+ projects shipped. $1.5M in direct contracts. ~$10M in documented client value across CPG, nootropics, frozen desserts, ingredient extraction, herbal and botanical formulation, and cosmetics. MSc in Biochemistry, six years in academia before that. That's how I know the difference between math that decides and math that impresses. Where my work tends to land: 🧊 Popsicles, frozen desserts, ice pops. Stabilizer system balance (xanthan, guar, LBG), sugar and syrup ratios, freezing-point depression, ice-crystal control, freezer-cabinet stability windows. Reactive formulators with every range hard-stopped to published literature. 🥤 Protein bars, protein beverages, protein isolates. Whey, casein, pea, soy, and hydrolysate selection. Sweetener and bitterness profiles, per-serving cost, label-claim feasibility, extraction yield, COGS per kilo, and breakeven curves across production scales. My protein-isolate model is used by clients across the agro-extraction industry to size processing lines before committing capital. 🌿 Botanicals and herbal products. Ingredient quality, MOQ math, supplier vetting, label compliance, formulation stability, extraction methodology. I also run a small herbal business myself, so I've felt every margin squeeze and ingredient-quote shock that clients bring to me. 💊 Supplements and nootropics. Claim feasibility, dose math, cost engineering, co-manufacturer scoping, channel-margin modeling. ✨ Cosmetics. Ingredient compatibility, parameter constraints, process simulation, scale-up math. 🛠️ What I actually deliver: A reactive browser-based calculator built around your real product, your real ingredient costs, your real production scale. Sliders for every variable that matters, with hard-stopped ranges grounded in published research. Plus the Excel back-end so your CFO can audit every formula. Plus a written diagnosis of what the numbers actually say. Plus implementation docs you can hand to your team. Typical turnaround: 5 business days for a tuned single-product engagement, 2 to 4 weeks for multi-product strategic models. Past custom engagements have run from $850 to $10,000, most landing in the $3,000 to $5,000 range depending on how many moving parts there are. 📊 Case study. David at Mora Cué Alimentos came to me with an equipment-selection question for a chia protein line. Three weeks later, with three product directions and three production scales modeled against real ingredient costs, channel margins, and capacity constraints, the answer was specific: protein concentrate at mid-scale, 41% gross margin. They built it. It works. 💬 What operators say: "Andres is very knowledgeable with great ideas and outstanding organizational skills." Cecilia Shepherd, CEO, Sound Science Nutrition "Andres was extremely helpful. I had a recipe emergency which he solved same day. I could go back to production with minimal disruption. Definitely will work again with him." Ismar Toromanovic, CEO, 3D Desserts "Andres is an outstanding chemist. I often cross-verify our models with his fundamental knowledge. I strongly recommend anyone looking for chemistry tutoring or overseeing complex calculations." Vishy Karri, CEO, Expert 365 "Congratulations on building this tool. It's really useful." David Olson, CEO, Mora Cué Alimentos ✅ A fit if you're a CPG, supplement, nootropic, cosmetic, or botanical founder at $1M+ in revenue or capital, making a real decision in the next 60 to 90 days. A co-man trial, an SKU launch, an ingredient swap, a scale-up. People tired of vibes-based pricing who want numbers they can defend in front of a board, a co-man, or a buyer. ⚠️ Probably not a fit if you're pre-revenue with a generic plan, shopping for the cheapest spreadsheet on the market, or looking for a formulator rather than a strategist. (I can refer you to good formulators if that's what you actually need.) Send me the decision you're sizing. If a model would help, I'll tell you. If it wouldn't, I'll tell you that too, in the first ten minutes.

Hello! I'm Dr. Hina Manzoor, a PhD in Biochemistry with over 10 years of experience in the pharmaceutical industry and extensive expertise in computational drug discovery, pharmaceutical documentation, and scientific research. I have successfully worked with pharmaceutical companies, research organizations, and international clients, delivering high-quality technical and scientific solutions remotely. My background combines pharmaceutical quality systems with advanced computational biology, allowing me to provide both regulatory documentation and research-based services. My Areas of Expertise Pharmaceutical Documentation GMP/cGMP Documentation Regulatory Dossiers (CTD/eCTD) Standard Operating Procedures (SOPs) Specifications & Methods of Analysis Batch Manufacturing Records (BMRs) Validation Protocols & Reports Process & Method Validation Equipment Calibration Documents Certificates of Analysis (COAs) Stability Study Documentation CAPA, Change Control & Risk Management Documents Training Manuals and Quality Documents Policies, Protocols, Forms & Log Sheets Artwork Review (Labels, Cartons, Leaflets & Packaging Literature) Computational Drug Discovery & Bioinformatics Molecular Docking Molecular Dynamics (AMBER & GROMACS) MM/GBSA Binding Free Energy Analysis Virtual Screening Pharmacophore Modeling Structure-Based Drug Design ADMET Prediction Protein-Ligand Interaction Analysis Drug Repurposing Studies RNA/miRNA Modeling QSAR and Machine Learning for Drug Discovery Scientific Research Research Paper Writing Literature Reviews Systematic Reviews Data Analysis Publication Support Manuscript Editing Journal Formatting Figure Preparation Thesis and Dissertation Support Programming & Data Analysis Python R Programming RDKit Pandas NumPy Scikit-learn Scientific Data Analysis Automation Scripts Business & IT Solutions Excel Automation & Inventory Management Company Profiles & Presentations Custom Software Solutions Technical Documentation Web-Based Applications Ongoing Technical Support Why Work With Me? ✔ PhD in Biochemistry with specialization in Computational Drug Discovery ✔ 10+ years of pharmaceutical industry experience ✔ Published author in high-impact international journals including Scientific Reports and PLOS ONE ✔ Practical experience in pharmaceutical quality systems, regulatory documentation, and analytical method validation ✔ Experience serving international clients through Upwork ✔ Strong communication, timely delivery, and complete confidentiality Whether you need pharmaceutical documentation, scientific writing, molecular docking, molecular dynamics simulations, computational drug discovery support, Python/R-based data analysis, or regulatory documentation, I am committed to delivering accurate, professional, and high-quality work tailored to your project requirements. Feel free to contact me to discuss your project. I look forward to helping you achieve your goals.

Medical & Scientific Writer with 6+ years of academic experience and proven freelance success. I specialize in biomedical research, literature reviews, and evidence-based scientific writing, helping clients turn complex data into clear, accurate, and engaging content.

As a PhD biochemist with over 40 years of experience in the biotechnology and pharmaceutical industries, I offer comprehensive consulting services in biotech project management, regulatory affairs, and process development. My expertise spans: Leading complex pharmaceutical projects as Projects Director at Biotechnology General for 14+ years Managing regulatory affairs (RA) for multiple biotech companies including Omrix Biopharmaceuticals and InterPharm Laboratories Developing and validating biotechnology processes at Kamada Ltd Evaluating innovative biotech projects at the Israel Innovation Authority I excel at bridging the gap between research and implementation, having worked across the entire pharmaceutical development pipeline - from basic research to regulatory compliance. I'm particularly skilled in: Project portfolio management Regulatory compliance and validation Process development and optimization Technical evaluation of biotech innovations I'm fluent in English , enabling me to work with international teams and documentation. As your consultant, I can help with regulatory strategy, process optimization, or project evaluation needs in the biotech/pharma space. I pride myself on delivering thorough, scientifically-sound solutions while maintaining compliance with industry regulations.