新北市新莊區3年以上碩士以上待遇面議
Dazzeon develops the world’s highest-purity acemannan (MannanPRO®, ≥90%) from Aloe vera for applications spanning immunity, mucosal/wound repair, oncology adjuvancy, and drug delivery. We operate ISO-22000/HACCP facilities and are building toward ISO-13485/GMP for devices and botanical drug pathways.
The Opportunity
We have a rich dataset (cell assays, organoids, RNA-seq, ROS/ferroptosis, wound healing, antiviral ALI models, nanogels, SHIME gut model data, etc.) and several commercialization tracks (B2B ingredient, medical device, oncology adjuvant). We need a creative, independent, and critical thinker who can connect the dots, propose smart next steps, and execute.
What You’ll Do
• Synthesize evidence: Audit and integrate internal datasets (HCT116 anti-tumor/ROS, ferroptosis signals, 5-FU co-treatment wound-healing rescue, NHBE ALI antiviral/TEER, RNA-seq DEGs, nanogel DLS/loading) into clear narratives and decision docs.
• Design & run experiments: Plan and coordinate in-vitro (cell culture, wound healing, viability, flow cytometry, RT-qPCR, western blot, etc), organoid studies, and small animal pilots via CROs/academia or internally as needed.
• Translate science to product: Convert findings into specifications for (a) oral MannanPRO® supportive-care use (e.g., 10 mg/10 mL/day), (b) mucosal medical device claims (ISO-10993 strategy), and (c) oncology adjuvant positioning.
• Regulatory & documentation: Draft protocols, statistical plans, reports, white papers, and submission-ready materials (e.g., device technical files, literature reviews, risk/benefit rationales).
• IP & publications: Scout prior art, support patent claims, and prepare manuscripts/abstracts with clean figures and reproducible methods.
• External partnerships: Source, brief, and manage CROs/academic labs; negotiate timelines, QC data, and budget.
• Data hygiene: Stand up an electronic lab notebook (ELN) and a lightweight data room (protocols, raw data, scripts, COAs).
What You’ll Bring
• MS/PhD (or equivalent experience) in Biomedical Science, Pharmacology, Biotech, or related.
• Proven independence in experimental design, critical analysis, and hypothesis generation.
• Experience interfacing with CROs/academia; comfortable writing SOPs, protocols, and reports.
• Excellent scientific writing (English a must; Mandarin a plus). Clear slides and figures.
• Bias for action, ownership, and pragmatic problem-solving in fast, changing contexts.
Nice to Have
• Oncology or mucosal biology background; familiarity with 5-FU models and adjunctive care.
• Organoid systems, RNA-seq analysis, DLS/zeta for nanomaterials, or device biocompatibility (ISO-10993).
• Regulatory familiarity (ISO-13485/QMS, TFDA/FDA device files, botanical drug pathways).
Success in Your First 90 Days
• Deliver a gap analysis that maps current evidence → near-term claims for (1) oncology supportive care and (2) medical device.
• Run/coordinate one confirmatory experiment (e.g., 5-FU + MannanPRO® wound-healing rescue with stats and visuals) and one translational pilot (e.g., palatability/PK-adjacent marker readouts for 10 mg/day oral use).
• Produce a publishable white paper (sales-ready) and a CRO workplan with timelines, budgets, and success criteria.
Contract & Compensation
• Project-based retainer or milestone structure; competitive and negotiable.
• Option to convert to full-time with equity participation.
• IP/confidentiality assignment required; occasional travel to partner labs.