育世博生物科技股份有限公司

【About the role】 We have an exciting opportunity for motivated individuals to join our CMC team working to develop cell therapies against cancer. The successful candidate will be expected to be a good team player, work with enthusiasm to execute assignments properly. 【Position Title】 (Sr.) Research Associate 【Location】 Taipei, Taiwan 【Reports to】 Principal Scientist 【Job Type】 Full-time 【Responsibilities】 • Support IND enabling related study. • Optimize immune cell culture process. • Develop new projects generally on a yearly basis. • Manufacture cell therapy products in a GTP lab as a core team member. • Conduct QC tests to secure safety, stability, and efficacy for our valuable products. • Establish and maintain the documentation system. 【Qualification】 • Passionate about research, self-motivated, values teamwork, willing to join the international cell therapy drug development field. • Good communication and interpersonal skills. • Familiarity with flow cytometry-based experiments is a must. • Familiarity with tumor-killing assay experiments is a plus. • Familiarity with GTP Lab practice is a plus. 【Academic and/ or working experience】 • MSc (or above) in life science or related fields (pharmacology, immunology, chemistry, and biochemistry). • 2+ years of working experience with cell culture as the primary duty.

【About the role】 We are seeking a highly motivated Associate Director, Antibody-Drug Conjugates (ADC) to play a key role in our ADC and related development programs. The ideal candidate will have a strong background in conjugation chemistry and linker-payload development/optimization with a proven track record leading successful ADC programs from discovery to IND submission. This role requires exceptional leadership and communication skills and will collaborate effectively with internal and external stakeholders, driving innovative solutions to advance our ADC technology. 【Position Title】 Associate Director, Antibody-Drug Conjugates 【Location】 Taipei, Taiwan. (CA, USA) 【Reports to】 Sr. Director of R&D 【Job Type】 Full-time 【Education /Background】 • Ph.D. in life sciences (oncology, immunology, chemistry, medicine, or related field) with a minimum of 8 years of industry experience, OR • BS/MS with at least 12 years of industry experience in ADC development. 【Responsibilities include but are not limited to】 • New Pipeline Development: Support the development of new products. • Literature Reviews: Conduct literature reviews, summarize scientific studies, and provide insights and critical analyses for ongoing projects. • External Collaboration • Due Diligence and Asset Integration: Support due diligence and asset integration activities as needed. 【Position Requirements & Experience】 • Provide scientific leadership and expertise in execution of ADC pipelines, including chemistry/bio-conjugation design, linker-payload design, conjugation process development and preclinical study design. • Manage project timelines, budgets, and resources to ensure alignment with corporate goals and timely delivery of milestones. • Prepare high-quality scientific documents, including peer-reviewed publications, regulatory submissions (e.g., IND), study reports, and presentations. • Collaborate with internal teams, including clinical, regulatory, and manufacturing, to integrate ADC development efforts seamlessly. • Partner with external CROs for ADC manufacturing and scale-up processes. • Analyze and interpret experimental data, providing actionable insights to internal and external stakeholders. • Support due diligence and integration of external assets into Acepodia’s pipelines. • May supervise and mentor junior scientists and research associates.

【About the role】 Acepodia seeks a highly motivated and experienced GMP Facility Engineering Manager to join our team. The GMP Facility Engineering Manager plays a crucial role in overseeing the design, maintenance, and operation of our facility and its associated equipment and systems, ensuring compliance with all Good Manufacturing Practices (GMP) regulations. This position demands a strong understanding of engineering principles, GMP guidelines, and project management methodologies, along with excellent leadership and communication skills. 【Position Title】 (Sr.) Manager of GMP Facility Engineering 【Location】 Taipei, Taiwan. 【Reports to】 CTO 【Job Type】 Full-time 【Responsibilities include, but are not limited to】 Project Management & Compliance: • Develop and implement comprehensive project plans for facility modifications, equipment upgrades, and new installations, including scope, timelines, resources, and budgets. • Manage the design, planning, construction, and maintenance of buildings, equipment, and other facilities to ensure compliance with GMP regulations. • Ensure that all engineering projects, initiatives, and processes conform to the organization's established policies and objectives. • Oversee the equipment, facilities, and utilities validation program, ensuring that all systems meet regulatory requirements and company standards. • Manage the department's operating budget and contribute to the development of the facility's annual and long-term strategic capital investment plan. Leadership & Collaboration: • Lead and actively participate in client interactions regarding equipment, facility, and utility lifecycle management. • Provide technical expertise and guidance to cross-functional teams, including manufacturing, quality assurance, and validation. • Manage and supervise third-party contractors and other internal service providers, ensuring that all work is completed according to procedures and health and safety standards. Maintenance & Continuous Improvement: • Identify and implement continuous improvement initiatives to optimize the performance and reliability of process equipment, utilities, and facilities. • Maintain and coordinate engineering maintenance support on off hours, as necessary. • Manage the calibration program and the Planned Preventative Maintenance program. Training & Safety: • Ensure that GMP is adhered to in all areas of work and that all employees understand and follow department objectives, company policies, and procedures. • Maintain a safe working environment and ensure compliance with all relevant safety regulations. • Oversee and ensure that all employees undergo GMP training to fully understand their roles and responsibilities in maintaining compliance. • Documentation & Reporting: • Contribute to the development and continuous improvement of Standard Operating Procedures (SOPs) and Standard Work Instructions. • Manage the process for creating SOPs and other documentation for facility equipment maintenance plans, manufacturing equipment maintenance plans, calibration SOPs, and the reliability engineering program. • Support Commissioning and Validation activities as needed. • Support Development Engineers and Equipment Vendors in delivering Equipment Turn Over Packages (ETOPs). • Work closely with all functional departments to ensure the continued maintenance of a validated environment according to cGMP and other regulatory requirements. • Deliver high-level reporting to directors and other leadership. • Operational Support: • Provide a daily presence in manufacturing and facility areas to support operations by troubleshooting and resolving complex technical issues.

【About the role】 We are seeking a detail-oriented and proactive Procurement Specialist to support our internal procurement operations. The successful candidate will be responsible for executing procurement-related tasks including, but not limited to, material number creation, supplier communication, contract management, and partial laboratory administrative support. This role plays a critical part in ensuring smooth procurement processes and effective vendor collaboration across the organization. 【Position Title】 Procurement Specialist 【Location】 Taipei City, Taiwan (onsite) 【Reports to】 Lab and Procurement Manager 【Job Type】 Full-time 【Education /Background】 • B.S. or M.S. in Supply Chain Management, Logistics, Business Administration, Industrial Engineering, or Life Sciences-related fields (Immunology, Oncology, Molecular Biology, Pharmacology, Chemistry, and Biochemistry) • 2+ years of experience in ERP procurement systems. 【Responsibilities include, but are not limited to】 • Execute internal procurement tasks in accordance with company procedures. • Create and maintain material numbers in the system. • Coordinate with suppliers regarding quotations, deliveries, and order confirmations. • Support contract management and documentation processes. • Assist in monitoring procurement schedules and ensuring timely fulfillment of procurement needs. • Provide administrative support related to laboratory management. 【Position Requirements & Experience】 • Prior experience in laboratory procurement execution. • Proficiency in ERP procurement systems. • Strong attention to detail and organizational skills. • Good communication and coordination abilities. • Experience in contract management and execution of outsourced service procurement projects. • Familiarity with procurement-related regulations and vendor compliance procedures.