Related Content
Download content relating to this event and topic.
Biologics Manufacturing Korea 2025 unites global leaders to showcase breakthroughs in AI, automation, biosimilars, and supply chain excellence. Join us to shape the future of biotech in Asia’s powerhouse market.
In the fast-paced and ever-evolving world of biopharma, South Korea continues to assert itself as a global leader, driving innovation through sustained R&D investment and groundbreaking initiatives from both the public and private sectors. South Korea’s exceptional performance in public health during the Covid-19 pandemic has solidified its reputation as a biotech powerhouse on the international stage.
As we look to the future, the 14th Biologics Manufacturing Korea 2025 aims to serve as the premier platform for collaboration, knowledge exchange, and strategic partnerships. This year's conference will delve into critical topics, including advanced strategies in upstream processing, the future of biomanufacturing through automation and AI technologies, insights on regulatory pathways for biosimilars and innovative approaches to downstream processing and supply chain optimization.
Biologics Manufacturing Korea 2025 will be co-located with the CGT East Asia 2025 and ADC & Bioconjugate East Asia 2025 events, enhancing the opportunity for interdisciplinary discussions and collaboration.
Join us at Biologics Manufacturing Korea 2025 to connect with key players shaping Korea’s biopharma landscape, including leaders from Samsung Biologics, Celltrion, SK bioscience, Hanmi Pharmaceuticals, Lotte Biologics, and more. If Korea is your gateway to growth in the biomanufacturing space, Biologics Manufacturing Korea 2025 is the destination where innovation meets opportunity.
View the Key Themes for
Biologics Manufacturing Korea 2025
Register today to secure your ticket.
Our selected experts will share insights on the latest trends, challenges, and developments in this dynamic field. Engage in unique discussions, learn about cutting-edge scientific discoveries, and explore the future of biopharmaceuticals with these influential thought leaders.
Sia Pheng Tan is an agile, strategic, and accomplished Quality Leader with a wealth of experience in global GMP regulated environments such as Amgen, GSK Biologics, Lonza, Alcon (Novartis), Baxter Healthcare, Becton Dickinson & Edwards Lifesciences. A successful track record across quality operations, audits, suppliers’ management, quality management system, validation & storage & distribution. A natural leader able to mentor, develop and manage high performing teams.
Dr. Saluja is the Head of Clinical Development at International Vaccine Institute (IVI), whose mission is to discover, develop and deliver safe, effective, and affordable vaccines for Global Health. He has 20 years of experience working in industry, academia and resource-limited settings in both patient care and clinical research. He joined IVI in 2017 and his main areas of research includes epidemiology studies, pre-clinical research, and vaccine clinical trials (phase I-IV). In his current role, he is responsible for capacity building in terms of trainings and infrastructure in low- & middle-income countries, designing clinical trials, grant writing, regulatory interactions, overseeing departmental activities like medical writing, study startup, study execution, regulatory submissions, pharmacovigilance and impact evaluation. He has many publications in national and international Journals to his credit. Dr. Saluja has received many awards & recognitions from academia and industry alike.
Woo Chi is Director of Cell Line Development group at Samsung Biologics, managing multiple client and internal development projects while representing the CLD team in various settings. During his first 6 months at SBL, his CLD team had projects with a record breaking pool and clone productivity, adapted process simplification to lower the development cost. His team also embarked on ambitious internal project to develop a license free cell line development platform to reach 6g/L titer, a transient expression system with competitive productivity and scalability as well as in-house-MCB facility inititives. Woo has more than 20 years of experience in pharmaceutical industry and academic research and has held roles across CHO cell line development, platform improvement, and assay development. Prior to joining Samsung Biologics, Woo served as a principal scientist at Evotec Biologics where he led cell line development projects and established a new CDO lab with automation capability. Woo holds a doctor’s degree in Genetics from Yale school of Medicine.
Sue Marchant is the Chief Product Officer at MasterControl, where she leads the strategic direction of quality, manufacturing, and intelligence solutions, with a strong focus on innovation, efficiency, and compliance. Backed by a talented Product Management and UX team, she defines the product vision and strategy while driving the development of exceptional, user-centric solutions. With more than 20 years of experience, including a decade in AI and data-driven platforms, she brings deep expertise in building cloud-native AI driven applications for the life sciences industry.
Kyung-il Cha is the Head of MSAT at GCBiopharma and a highly accomplished professional with over 21 years of experience in the biopharmaceutical industry. He has primarily focused on New Product Introduction projects related to various plasma derivative products and has expanded his expertise to include recombinant proteins and mRNA technology. He is also experienced in diverse multicultural working environments at a manufacturing site located in Montreal, Canada. He has extensive experience in manufacturing and quality, especially in regulatory filing and inspection from agencies around the world. One of his most notable recent achievements as a project leader was the approval of an immune globulin intravenous product called Alyglo™ by the US FDA. In his current role as the Head of MSAT, he is responsible for developing innovative products in plasma derivatives, recombinant proteins, and mRNA, as well as manufacturing investigational medicinal products
Dr. Jonna Sankaraiah is a distinguished pharmaceutical scientist with over 16 years of global experience in biopharmaceutical and pharmaceutical process development. Holding a Ph.D. in Pharmaceutics, he currently serves as Tech Transfer Lead at Medytox Inc., South Korea, where he leads end-to-end technology transfer, scale-up, and validation of biologic products, including monoclonal antibodies (mabs), botulinum toxins, vaccines etc.. Dr. Sankaraiah has previously held senior roles at Celltrion, Dr. Reddy’s, and Zydus Lifesciences, contributing to successful product launches for regulated markets such as the U.S. and EU. His expertise spans QbD-based formulation design, process characterization, regulatory compliance, and lifecycle management across both biologics and complex generics (Sterile drug products). Recognized for strategic leadership and cross-functional coordination, he has played a pivotal role in product commercialization, global tech transfers, and regulatory submissions. With deep technical acumen and operational insight, Dr. Sankaraiah is a trusted expert in Manufacturing Science and Analytical Technology (MSAT) and a valuable voice in global pharmaceutical innovation
Ji Hyeong Kim is a professor at the Korean National Institute for Bioprocessing Research and Training Center, Yonsei University. He has over 12 years of experience in the biopharmaceutical and medical device industries. He has also undergone various regulatory inspections by the U.S. FDA, Korea MFDS (a PIC/S and ICH participating authority), and Medical Device Certifications (CE MDD/IVDD, ISO 13485). As a quality specialist, He contributed to several product approvals during these processes. His extensive experience with Quality Management Systems enables him to efficiently solve problems; at Hanmi Pharmaceuticals, he resolved over 300 deviations and planned corresponding CAPAs. After obtaining a Master's degree in Education, he is currently employed in the biopharmaceutical education sector. He is responsible for providing training in quality assurance and quality control to various universities and pharmaceutical companies in Korea, and conducts international collaborations, including WHO training programs.
Hyemi Kim is a seasoned expert in IT and process innovation, currently leading the Digital Innovation Office’s DX Team at SK Bioscience. She holds a degree in Atmospheric Sciences from Yonsei University and completed the CAIO program at KAIST, integrating AI technologies into her work. At Samsung Group, she spearheaded projects enhancing operational efficiency across various sectors using Six Sigma, TRIZ, and SAP. Her tenure at Samsung Biologics focused on IT strategy, ERP enhancement, data integrity, GxP processes, and digital governance. As a consultant, she collaborated with private and public entities on digital platform models. At SK Bioscience, Hyemi drives digital innovation strategies, applying AI and digital technologies in R&D, manufacturing, and business development. The next-generation ERP system is set to launch in the first half of 2025. In this conference, she will share experiences on 'Automation and Bioprocessing 4.0' in bio/pharmaceutical companies.
Heonchang Lim is the Director of Formulation Development at Samsung Biologics’ CDO division, where he leads a team dedicated to developing innovative drug formulations. With over 15 years of experience in the biopharmaceutical industry, Heonchang specializes in protein drugs and vaccines.
He has successfully managed more than 50 formulation development and non-GMP DP manufacturing projects. In September 2022, he helped launch DEVELOPICK™, a platform that evaluates target molecules. Prior to joining Samsung Biologics in 2017, Heonchang served as a scientist at LG Chem, where he conducted R&D for purification and formulation development in multiple vaccine and protein drug projects.
He holds a master’s degree in medicine from Seoul National University and a bachelor’s degree in molecular biology from Catholic University.
Dea Marsendah, a true vaccine practitioner and biotech enthusiast. With over 13 years of experience in life sciences and vaccine manufacturing, she now leads Learning & Development at PT Bio Farma; building future-ready teams through global partnerships, quality learning systems, and innovation-driven programs. With a strong background in biotechnology and a Professional MBA, Dea is passionate about turning knowledge into real impact; for people, for processes, and for public health.
Dr. Darshana Jain is a seasoned pharmaceutical professional with over 11 years of experience across research, sales, business development, and technical roles. She began her career at Cipla Ltd., focusing on innovative formulation and product development. She then joined Roquette Pharma, where she has held multiple positions, including Regional Sales, Global Account Management, and now serves as Technical Development Manager for Asia and China. In her current role, Dr. Jain leads technical project development and innovation initiatives, offering support across Roquette’s excipient portfolio for both pharma and biopharma clients. She collaborates closely with R&D teams to drive customer-centric solutions and troubleshoot complex formulation challenges. Dr. Jain holds a Ph.D. in Pharmaceutical Technology from CU Shah College of Pharmacy, Mumbai, and is a recipient of the prestigious INSPIRE-DST fellowship. She also has two patents, three book chapters, and several scientific publications to her name.
Choose a plan that fits your role, company, and industry.
Standard
Applicable to company profiles (headquartered within the APAC region):
Job Profiles: Manufacturing, Bioprocessing, Production, USP, DSP, Operations, Site Heads, Drug Substance and Product Manufacturing, Process Development, Quality, Analytics and other related technical designations
Standard
Applicable to company profiles (headquartered outside of the APAC region):
Job Profiles: Manufacturing, Bioprocessing, Production, USP, DSP, Operations, Site Heads, Drug Substance and Product Manufacturing, Process Development, Quality, Analytics and other related technical designations
Standard
Applicable to company profiles:
Job Profiles: Business Development, Marketing, and Sales
Be the first in line! Register your interest now to get exclusive access to Super Early-Bird tickets - the lowest prices available - before they go live.
Join the roster of esteemed colleagues to discuss what you or your company are bringing to the biopharmaceutical industry.
Contact the IMAPAC to learn about our sponsorship process, rates and more.
Visit the event page to view more content.
Download content relating to this event and topic.
Visit the event page to view more content.
Visit the awards page to view more content.
To stay informed about event updates, including date, venue, and agenda, please subscribe to our newsletter on our event website. You can also follow our official social media channels for real-time updates and announcements.
The conference will provide a comprehensive learning experience covering various aspects of the dynamic biopharmaceutical industry, ensuring attendees gain valuable insights and knowledge.
We are committed to ensuring the safety and well-being of all attendees. We will implement rigorous safety measures in line with local health guidelines and regulations. Specific safety measures will be communicated closer to the event date to ensure they align with the most up-to-date health recommendations. Rest assured, your safety is our priority.
Yes, we have a cancellation and refund policy in place. Please refer to our “Cancellation Policy” on our website for details on how to request a refund if you are unable to attend.
We welcome presentation submissions. If you’re interested in speaking at the event, please visit this page on our website for submission guidelines and deadlines.
Our event is designed to cater to a wide range of professionals within the biopharmaceutical industry, including researchers, scientists, executives, regulatory experts, and professionals involved in drug development and manufacturing.
Participants can expect to gain insights from industry experts, network with peers, and stay up-to-date with the latest trends and innovations in biopharmaceuticals
Yes, we have networking sessions, workshops, and social events scheduled throughout the event to facilitate connections and collaborations among attendees.
Yes, we offer sponsorship and exhibition opportunities for businesses and organizations. Please visit our this page on our website for more information.
To register for the event, you'll find multiple "register" buttons on this page to get started. You’ll find detailed instructions and options for registration, including pricing and deadlines.
Don't miss out on unique networking, speaking and sponsorship opportunities.