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BOS Basel 2025 Programme

BOS Basel 2025's scope is primarily development-stage CMC outsourcing for both Small Molecules and Biologics, as well as covering Novel Therapeutic Entities.

We have a single-track programme consisting of high-quality presentations and drawing from the diverse organisation types in the community including multinational pharmaceutical companies, speciality pharma, SME biotech, CRO/CMO and Consultants. Our programme consists of the following modules:

Outsourcing Business Process
Exploring strategies and processes driving sourcing and procurement of R&D services

Technical Operations
Exploring the technical elements of outsourcing discovery R&D, Drug Substance Outsourcing, Analytical Development Outsourcing, Drug Product Outsourcing for Biologics and Small Molecules.

Outsourcing Case Studies
Building on the Technical Operations sessions, demonstrating outsourcing approaches to real life scenarios.

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Day 1 - 11th June 2025

Time BOS Basel Programme
08:00 - 09:00
Registration and Partnering (10 min Partnering Slots)
09:00 - 10:30 Outsourcing Process and Strategies
09:00 - 09:30
Considerations for Developing and Executing a CMC Outsourcing Strategy
Mr Julius Simonelli, Executive Director, Strategic Outsourcing - Technical Research & Development, Novartis
About the speaker


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09:30 - 10:00
Sourcing and Procurement Toolkit for the Biotech Start Up!
Kirsty Keith, Director of Manufacturing & Outsourcing, Immunocore
photo of Kirsty Keith
About the speaker

Kirsty is Director of Manufacturing and Outsourcing at Immunocore. She is responsible for execution and oversight of outsourced manufacturing of GMP products for clinical trials and commercial supply.

Immunocore is a pioneering T Cell receptor biotechnology company, developing a new generation of transformative medicines addressing unmet needs in cancer, infection and autoimmune disease.

Prior to Immunocore Kirsty spent over 20 years at GSK in small molecule pharmaceutical manufacturing and supply. 15 of those years were spent leading various manufacturing operations, after which she joined GSK's External Supply Organisation to lead the European region. At the beginning of this year Kirsty joined Immunocore to expand her experience in the Biopharmaceuticals arena.

Kirsty is also a certified executive coach and is currently studying for an Executive MBA at Bayes Business School in London.





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10:00 - 10:15
Application of AI in the Pharmaceutical Outsourcing Process
Dr Frederik Deroose, VP Chemistry and CMC, Scientist.com
10:15 - 10:30
Speaker to be Confirmed
10:30 - 11:00
Coffee and Partnering
11:00 - 12:00 Outsourcing Case Studies
Chair: Dr Miranda de Jager, Owner/Principal Consultant CMC, M3 Pharma Consultancy
11:00 - 11:20
CDMO Sourcing for Clinical Stage Biotech: Strategic Dilemmas
Michel David, VP CMC, Manufacturing and Supply Chain, NOEMA Pharma AG
photo of Michel David
About the speaker

With over 25 years of experience in Pharmaceutical Manufacturing and Development, Michel leverages his broad cross functional experience covering the End-to-End supply chain, taking molecules to market, as well as managing partnership with external providers. Prior to joining NOEMA, Michel held several responsibilities in Roche Pharma, including; Leading a global small molecules Drug Product Manufacturing Site where he launched new products, Developing and implementing global manufacturing network strategies, Setting up external manufacturing operations and driving Operational Excellence. Michel started his career at Aventis as a Chemical process engineer in Pharma Development. Michel is a strategic thinker, with business acumen and a passion for driving execution and delivering safe and compliant drugs to the patients. Michel holds a MSc. in Chemistry, a Chemical Engineering degree from ENSCP, Paris and an MBA from INSEAD.
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11:20 - 11:40
Gold Sponsor Presentation: Siegfried
11:40 - 12:00
Considerations for Selecting a Data Platform to Accelerate Research
Dr Lotti Frauchiger, Head CMC, Molecular Partners
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12:00 - 13:30
Lunch and Partnering
13:30 - 15:30 Technical Operations Outsourcing
Chair: Dr Reinhard Karge, Executive President, RCJ unlimited - Karge consulting
13:30 - 14:00
Discovery and process development of the new Antibiotic Zosurabalpin
Dr Patrizio Mattei, Distinguished Scientist, Medicinal Chemistry, F. Hoffmann-La Roche Ltd.
Dr Ernesto Santandrea, Senior Principal Scientist, F. Hoffmann - La Roche
photo of Patrizio Mattei
About the speaker

Patrizio Mattei is an Expert Scientist, Medicinal Chemistry at the Roche Innovation Center Basel. Before joining Roche in 1999, he earned a Doctor of Sciences degree from the ETH Zürich and was a postdoctoral research fellow at The Scripps Research Institute in La Jolla, California.
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About the speaker


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14:00 - 14:30
Presentation to be Confirmed
14:30 - 15:00
Building Robust CDMO Selection Strategies for Biologics Development
Mr Jay Howlett, Director, External Operations, Vir Biotechnology
photo of Jay Howlett
About the speaker

Jay Howlett is the Director of External Operations for the mAb platform at Vir Biotechnology in San Francisco, CA. He has worked in the biotechnology industry for over 20 years in the small biotech, innovator company and contract manufacturing spaces. Previous to Vir, Jay spent 15 years at Genentech/Roche where for 10 years he worked on commercial product transfers (DS, DP and packaging) to support both internal and external needs world-wide and then 5 years in the development space within external manufacturing supporting CMC teams. His contract manufacturing career started at DSM Biologics in Montreal, Canada for early and late stage DS biologics manufacturing. Jay holds an undergraduate degree in chemical engineering from the University of Waterloo (ON, Canada) and a Master of Science in Biology/Biotechnology from Carleton University (ON, Canada).
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15:00 - 15:15
Gold Sponsor Presentation
15:15 - 15:30
Gold Sponsor Presentation
15:30 - 16:00
Coffee and Partnering
16:00 - 17:00 Outsourcing Case Studies
Chair: Dr Rudolf Hausmann, Partner/Consultant, Viopas Venture Consulting
16:00 - 16:20
Amorphous drug Formulations with Microporous Magnesium Carbonate. Dr Marc Willuhn, Head of Process Development, Disruptive Pharma
16:20 - 16:40
Gold Sponsor Presentation
16:40 - 17:00
In-house Manufacture or External Sourcing of Gene Editing Reagents to support the Growing Cell and Gene Therapy Business
Dr Ulrich Rümenapp, Senior Program Lead, Bayer AG
photo of Ulrich Rümenapp
About the speaker

Dr. Rümenapp is based in Wuppertal, Germany and working within the Product Supply Biotech organization of Bayer AG, where he is responsible for the transfer of Bayer’s pipeline candidates (antibodies and antibody-drug-conjugates) to external manufacturing partners and regulatory submission and launch preparations.

Prior to working in Development, Dr. Rümenapp was Head of Biotech Projects in Product Supply Biotech at Bayer, where he was responsible for contract manufacturing partnerships in the field of biotechnological drug substances and drug products and interdisciplinary project management with the goal to ensure market supply. Before it was acquired by Bayer, Dr. Rümenapp hold a similar position at Schering AG, and before that, he worked in the Production & Logistics department of Schering, where he was responsible for production aspects of in- and out-licensing deals, due diligences, and product acquisitions of small molecule products and biologics. Dr. Rümenapp studied chemistry and holds a Ph.D. in biosciences. He worked several years in academic research in the field of signal transduction and as an assistant teacher in the field of general pharmacology. Today, Dr. Rümenapp area of expertise is the set-up and management of external relationships for the development and supply of bio-pharmaceutical products. He has more than 20 years of experience in the bio-pharmaceutical industry.To correspond with Dr. Rümenapp, please contact him at [email protected].
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17:00 - 19:00
Drinks Reception
Time BOS Basel Programme
08:00 - 09:00
Refreshments and Partnering
09:00 - 11:00 Technical Operations Outsourcing
09:00 - 09:30
Early Phase to Full Scale Manufacturing. An Overview of Biocatalysis at Novartis Pharma
Florian Kleinbeck, Director of Biocatalysis, Novartis Pharma AG
photo of Florian Kleinbeck
About the speaker

Florian Kleinbeck is Director of Biocatalysis at Novartis in Basel (Switzerland). Following a PhD in natural product synthesis at ETH Zurich (Switzerland) and a postdoc in asymmetric catalysis at UC Berkeley(USA), he joined Novartis in Chemical & Analytical Development. Since his start, he contributed as
process chemist and project leader to late phase development projects and transfers into production for both small molecule and oligonucleotide projects. In addition, he extensively supported technical lifecycle management activities of established brands. In early 2024, he took on the role as team lead of the
Biocatalysis Team in Chemical & Analytical Development at Novartis.
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09:30 - 10:00
How the Biosecure Act ,and Wider Geopolitical Trends, are Shaping Manufacturing Sourcing Strategies
Dr Carl Hitscherich, Head of External Supply, Alnylam
About the speaker


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10:00 - 10:30
Antibody Drug Conjugates: Panorama, perspectives and manufacturing challenges
Dr Olivier Cochet, Head Pharmaceutical Development, Debiopharm International SA
photo of Olivier COCHET
About the speaker

Debiopharm International is a highly focused company that develops drugs and therapies with a view to bringing novel biopharmaceuticals to market. The business strategy is to create partnerships for the in-licensing of biologics and small molecules from biotechnology and pharmaceutical companies as well as academic institutions worldwide.
Lead the Pharmaceutical Development department to ensure the development and manufacturing of products tailored to the needs of patients
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10:30 - 10:45
Gold Sponsor Presentation
10:45 - 11:00
Gold Sponsor Presentation
11:00 - 11:30
Refreshments and Partnering
11:30 - 12:30 Outsourcing Case Studies
Chair: Dr Harald Hufsky, MBA, Sr. Pharma Consultant, Dr. Harald Hufsky Pharma Consulting
11:30 - 11:50
Large-Scale Synthesis of LPA1-Receptor Antagonist ACT-1016-0707. Dr Florence Masse, Senior Research Associate, Chemistry Process R&D, Idorsia Pharmaceuticals
11:50 - 12:10
Gold Sponsor Presentation
12:10 - 12:30
Case Study for CDMO Selection : Case Study for a Phase 1 Recombinant Protein Candidate
Yogeshwar Bachhav, Director (Consultant), AiCuris Anti-infective Cures AG
photo of Yogeshwar Bachhav
About the speaker

Yogeshwar Bachhav is a pharmacist by training and has PhD in advanced drug-delivery systems from ICT, Mumbai (India). He has around 16 years of post-PhD experience in Europe in the field of pharmaceutical development of investigational drugs. He has contributed to the success of the clinical candidates ranging from preclinical to phase 1, 2, and 3 trials followed by commercial launch. Yogesh has worked as a Research Scientist for around four years on a collaborative project between Pantec Biosolutions AG (Lichtenstein) and University of Geneva, Switzerland. After this, he has worked as a Formulation Manager at Debiopharm Group, Lausanne, Switzerland, for around four years in the capacity of a lab head, where he successfully developed preclinical and clinical formulations for oncology indication. Currently Yogesh is working as a Associate Director (Consultant) at AiCuris Anti-infective Cures AG Germany and responsible for pharmaceutical development of investigational drugs in the domain of innovative anti-viral and anti-bacterial drugs. Yogesh’s expertise in the field of advanced drug-delivery system comprises pre-formulation, formulation development of small molecules and/or peptides for oral, dermal, and parenteral applications. Also, he has exposure to in-house development and outsourcing these novel dosage forms. Besides several publications in the targeted formulation field, Yogesh is a well-known expert with over 30 conference proceedings and has been named Wiley-VCH in the same book series titled Innovative Dosage Forms: Design and Development at Early Stage. He is also serving as visiting faculty at reputed Pharmacy Schools in India.
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12:30 - 14:00
Lunch and Partnering
14:00 - 15:00 Panel Discussion - Navigating Geopolitical Headwinds in Pharmaceutical Outsourcing
Dr Tarita Qveflander, Head of Strategic Sourcing and Direct Procurement, Swedish Orphan Biovitrum AB
Dr Carl Hitscherich, Head of External Supply, Alnylam
About the speakers
photo of Tarita Qveflander
About the speaker

Tarita Qveflander is the Head of Strategic Sourcing and Direct Procurement at Sobi – Swedish Orphan Biovitrum AB. Tarita has 18+ years of pharmaceutical operations, supply chain, and procurement experience. She also has extensive knowledge of global API/drug substance, drug product, and finished goods supply chain, including hands-on technical expertise and a deep understanding of quality and GMP regulations.
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Carl Hitscherich     
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15:00 - 16:00
Conference Close & Drinks Reception