台灣浩鼎生技股份有限公司

Company Introduction

151 Employees
台北市南港區忠孝東路七段508號6F(台北生技園區)
Contact Person
李小姐
Phone
暫不提供
台灣浩鼎 (OBI Pharma Inc.) 是一已推進至臨床階段的全球性癌症新藥公司,除設於台灣之企業總部及研發中心外,在美國和澳洲均有子公司。它是由美國知名的成功生技創業家張念慈博士 (Dr. Michael Chang) 於2002年所創立,2012年公開發行,2015年在台北櫃買中心正式上櫃交易 (TWO.4174)。 台灣浩鼎專注於癌症療法的創新與研發,旨在開發首創型 (first-in-class) 及同類最佳(best-in-class) 的突破型新藥,希望以「台灣製造」品牌,行銷全世界,並為醫療需求尚未被滿足的患者,提供新的治療選擇。 OBI 核心價值,除了極具前景的 Globo 系列 (如 Globo H) 癌症治療疫苗外,更聚焦於提供患者一系列獨特的抗體藥物複合體 (ADC) 新藥。 這些不斷擴展的產品組合,包括以TROP2、Nectin4、HER2 等一系列癌症標靶所開發的 ADC 產品。它們均以浩鼎獨家開發的兩個 ADC 技術平台所構建。兩個平台各具特色,都可「量身訂製」各種ADC;透過抗體醣位點的修飾,可精準將小分子藥物鏈接,憑藉此「即插即用」的策略及平台放大生產之潛力,使得 ADC 開發相對簡單而有效率。 OBI 正致力於將其擁有的 ADC 技術平台商業化,並期待與生技和製藥公司合作,實現首創型 (first-in-class) 和同類最佳 (best-in-class) 候選藥物的進一步開發。 OBI Pharma Inc. (OBI) is a global clinical stage oncology company that is headquartered in Taiwan. The company also has subsidiaries in the United States and Australia. It was founded in 2002 by Dr. Michael Chang, an accomplished biotech entrepreneur in the United States. Its stocks were issued publicly in 2012. Subsequently, the company was successfully listed on the Taipei Exchange (TWO. 4174) in 2015. OBI focuses on innovative research and development for cancer therapies and aims to develop “first-in-class” and “best-in-class” ground-breaking drugs. It aspires to market these drugs worldwide with a “Made in Taiwan” branding and to provide new treatment options for patients with unmet medical needs. The core value of OBI lies in its passion to develop and deliver a portfolio of unique antibody-drug conjugates (ADC) drugs for patients, in addition to its promising Globo series (e.g., Globo H) of cancer therapeutic vaccines. This evolving portfolio includes a spectrum of cancer targets, such as TROP2, Nectin4, HER2, etc. These ADCs are built based on two distinct ADC technology platforms, each with different characteristics. Both platforms are customizable and offer a “plug-and-play” advantage through a specialized site-specific conjugation using a proprietary enzyme. With the added value of scalability, these “plug-and-play” technology platforms enable ADC development to be relatively simple and efficient. OBI is interested in commercializing its ADC technology platforms and looks forward to collaborating with biotech and pharmaceutical companies by enabling “first-in-class” and “best-in-class” therapeutic candidates for further development.

Industry Sector
生化科技研發業
Related Links
Company Website

Main Products

1. Adagloxad simolenin - Globo H 主動免疫抗癌新藥 2. OBI-833 - Globo H 主動免疫抗癌新藥 3. OBI-3424 - AKR1C3 前驅型藥物 4. OBI-992 - TROP2 ADC 抗體藥物複合體新藥 5. OBI-902 - TROP2 Glycan ADC 抗體藥物複合體新藥 6. OBI-904 - Nectin-4 Glycan ADC 抗體藥物複合體新藥 7. BsADC - TROP2, HER2 Glycan ADC 雙特異性抗體藥物複合體新藥

Benefits

「獎 金 」:生日禮金、三節獎金 「休 假 」:週休二日、陪產假、年假、有薪病假5天、第一年即享有10天(以上)特休 「保 險 」:勞、健保、意外險、壽險、員工體檢、勞退提撥金 「補 助 」:結婚、生育、教育訓練補助 「其他 」:舒壓按摩、交誼津貼、交通津貼、彈性上下班(中午休息1.5個小時),飲料點心免費提供、家庭日、春酒晚會、不定期餐敘、員工國內旅遊、社團活動(如: 空中瑜珈、Keep Fit、太極拳、羽球、桌遊等)、不定期講座 • 飲料點心免費提供

Company & Workplace

Jobs

Senior Procurement Supervisor 台灣浩鼎生技股份有限公司
Salary negotiable
台北市南港區
5年以上
1. Evaluate and compare supplier quotes and proposals. Collaborate with internal teams, such as R&Ds, Legal, Finance and PMs, to ensure accurate and timely fulfillment of offers. 2. Ensure the effective and efficient management of procurement processes by coordinating with suppliers and internal stakeholders to meet service level and cost objectives. 3. Monitor supplier performance and resolve issue impacting delivery, quality, or cost. 4. Prepare and maintain purchasing reports and records. Ensure the information within is accurate, comprehensive, and up-to-date so as to drive insightful decisions. 5. Develop and maintain strong relationships with suppliers to ensure high quality and timely delivery of goods.
Full-time
Manager/Director
English Required
9/16 Updated
R&D Senior Scientist I/II for clinical pharmacology 台灣浩鼎生技股份有限公司
Monthly Salary NT$ 47,000+
台北市南港區
2年以上
• Represent clinical pharmacology for the assigned study team to support clinical study conduct from clinical pharmacology perspectives. • Translate nonclinical data to human efficacious dose projection. • Design experimental PK or PKPD studies in animal or human to better understand the clinical pharmacology of compound in development. • Conduct Non-Compartmental Analysis (NCA) for nonclinical and clinical PK studies and writing the PK reports. • Work with vendor or perform in-house population PK and PKPD analyses. • Responsible for preparation of regulatory submissions such as IND submission, and response to health authority’s questions with respect to clinical pharmacology.
Full-time
Mid to Senior Level
English Required
9/16 Updated
R&D-Scientist II/Senior Scientist I (Formulation Development) 台灣浩鼎生技股份有限公司
Salary negotiable
台北市南港區
2年以上
1. Formulation Development: • Design/Develop and optimize Drug Substance/Drug Product formulations for dosage forms (injectables) of large molecule (mAbs, ADC, …etc.). • Conduct studies and assess the impact of formulation changes on product CQAs. 2. Process Development: • Design and execute process development studies of DS/DP formulations from the lab-scale to CDMO production. • Evaluate manufacturing processes and recommend improvements to enhance efficiency and product quality. 3. Documentation and Compliance: • Support regulatory submissions, including INDs and NDAs/BLAs, ensuring compliance with regulatory guidance. • Maintain accurate and thorough documentation of all research and development activities. 4. Cross-Functional Collaboration: • Work closely with colleagues in Analytical, Biology, Clinical, Regulatory, and Quality Assurance to support product development initiatives. • Participate in project teams, contributing scientific expertise to drive successful outcomes. 5. Troubleshooting: • Investigate and resolve formulation and manufacturing issues, applying scientific principles to develop effective solutions.
Full-time
Mid to Senior Level
9/11 Updated
Lab part-time assistant (R&D: Analytics) 台灣浩鼎生技股份有限公司
Hourly Wage NT$ 183+
台北市南港區
經歷不拘
1. Produce testing buffer and solutions for the lab. 2. Order and track lab supplies. 3. Replenish test bench supplies as needed. 4. Prepare lab sample for testing and analysis. 5. Ensure all equipment is working properly and perform minor instrumentation maintenance. 6. Complete record logs and other administrative duties as requested. 7. Follow all Standard Operating Procedures to ensure safety and quality standards. 8. Other tasks assigned by supervisor.
Part-time
Entry-level
9/11 Updated