As Principal Scientific Affairs, Dr. Bettine Boltres is supporting the scientific exchange between West and the pharmaceutical industry. This is complementing work as Product Manager for Schott Pharmaceutical Tubing, where she provided scientific consulting for glass primary packaging.
Since 2015 Bettine is an active member of the USP Packaging and Distribution Expert Committee as well as the ISO TC76/WG 4 on elastomers. Additionally, in 2018 joined the European Pharmacopoeia Commission Group of Experts 16 (elastomers and plastics) and the GLS Working Party (glass).
Since January 2019 she is also a member of the PDA Board of Directors, actively supporting the role of PDA in the global pharma world. She is active in the PDA Glass Handling Task Force and co-chairing the European PDA Interest Group Packaging Science as well as the Pharmacopeia Interest Group.
In 2015 she published the book ""When Glass Meets Pharma"".
She is a frequent speaker at industry conferences and has chaired and moderated several conferences for the PDA and other formats. This is adding to numerous trainings and publications that she has provided.
Dr. Boltres is a (bio)chemist by training, with a diploma in chemistry and a PhD in biochemistry.
YongHua Gao is Deputy Secretary-General at the China National Pharmaceutical Packaging Association. Graduated from West China Medical University, pharmacy chemistry is the major profession. 8 years work experience of pharmaceutical research, producing, and quality management in pharmaceutical factory. Since 2002, working in China National Pharmaceutical Packaging Association, responsible for the technology and research project on Pharmaceutical Packaging.
Sinue Gomez, Product Development Manager for Corning Pharmaceutical Technologies, currently leads the design and development of products for parenteral packaging that meet customer and industry requirements at Corning’s Research and Development facility, Sullivan Park. Sinue specializes in glass composition, processes, and properties that deliver needed product performance attributes.
Sinue earned her B.S. in Materials Science from Universidad Simon Bolivar, Venezuela, and her Ph.D. in Materials Science from The University of Connecticut. She has co-authored 14 peer-reviewed articles and has over 50 granted patents.
Jacqueline (Jacquie) Hollands leads and develops MilliporeSigma’s initiatives and programs that meet the sustainability needs for customers. She has implemented product recycling options, such as the Biopharma Single-Use Product Recycling Program and the ech2o™ Lab Water Cartridge Recycling Program. Currently she is working on developing innovative recycling solutions for the life science industry.
Jacquie has more than 25 years of experience within the life science industry, holding positions in biological research, training, sales and sales support, as well as serving as program manager on several product development projects for detection instrumentation platforms.
Throughout her career, Jacquie has demonstrated an ability to communicate technical material clearly and effectively to all levels of audience, and to develop and implement initiatives that create positive change, efficiency and increased profitability.
Prior to her tenure with MilliporeSigma, Jacquie spent seven years in various roles in the life science industry—managing customer relationships, serving as a technical specialist and developing programs and products related to imaging and detection systems.
Jacquie holds a bachelor’s in biological sciences from Hood College and has nine years of lab experience, having performed multiple techniques in the fields of molecular and protein biochemistry, immunology and cell biology at Johns Hopkins University, Northwestern University and Oxford University.
Dr. Klein is a regulatory, scientific, CMC Expert with 23 years (1995 – 2017) of experience as a Senior Review Chemist of new drugs in CDER/FDA where he received upon retirement the FDA Distinguished Career Service Award (2017) from the FDA Commissioner. While at the FDA, Don significantly contributed to developing FDA policies for pharmaceutical packaging, comparability protocols, and drug master files. With respect to post-approval changes, his last 12 years were dedicated to the CDER CMC post-marketing division where he was a Senior Review Chemist and a CMC Lead (2013 – 2017). In addition, Don worked with fellow FDA Experts and Industry to resolve drug shortage issues from 2005 to 2017. Prior to starting a Consulting Company (7/2019) with his wife, Lynda Taskett, Dr. Klein was a CMC Consultant at parexel (9/2017 – 6/2019). In his professional career he has either reviewed or drafted applications in the following therapeutic areas: Oncology, AIDS, Neurology, Psychiatric, Metabolic/Endocrine, Dermatology, Pulmonary, Analgesic, Radiopharmaceutical; and OTC. Don has been an invited speaker at AAPS, PDA, and RAPS Conferences and had presented several seminars (1999 – 2017) within the FDA as well as representing the FDA. He received a B.S. in Chemistry from Allegheny College (1982) and a Ph.D. in Synthetic Organic Chemistry from Emory University (1988).
Brett Marshall is the Corporate Head, Quality Assurance for Zuellig Pharma based in Singapore, the largest healthcare services group in Asia. Based in Singapore, Brett has reporting lines from Quality Assurance Heads in 13 Countries and oversight of Clinical Reach Operations in another 4 Countries. Brett is passionate about Quality 4.0 and how the QMS of the future, enabled by digitization, will bring more effective Quality Risk Management in increasingly complex life science supply chain and regulatory landscape.
Originally from Melbourne, Australia, Brett has a Bachelor Degree in Transport & Logistics Management from RMIT. He has over 25 years’ experience in positions of Executive Management, Logistics & Supply Chain, Business Process Transformation and Quality Assurance, more than 15 years in the Pharma Industry, and has spent nearly 25 years in Asia living in Indonesia, Thailand, the Philippines, Bangladesh and now Singapore.
Roman Mathaes is Head of Pharmaceutical Services at Lonza DPS. In this role, he is responsible for primary packaging development and testing as well as device testing, tox and technical batch drug product manufacturing and the Lonza DPS lab automation group.
In his previous role at Lonza DPS, he was a Sr. Group leader in the Analytical Department performing drug product stability studies and leading the Lonza particle core facility.
Before his assignment Roman, worked within the Roche/Genetech network Basel/San Francisco.
Roman is a pharmacist by training and holds a PhD in pharmaceutical technology.
Roman is a adjunct member of the Pharmaceutical Department University Basel and authored 30 research papers in the field of Biotech Drug Product Development.
Corinne Ondo leads the sourcing of Innovation and the sourcing strategy of glass primary containers for Merck Healthcare.
Through her team, she also coordinates the procurement of secondary packaging activities for various manufacturing sites in Europe and Latin America.
Before joining Merck in 2015, she had over 20 years of international experience in the luxury business, consumer goods, automotive and oil & gas industry.
She is an engineer, graduated from French ESIGELEC Graduate School of Engineering.
Dr. Yusuf Oni is a Principal Engineer at Bristol-Myers Squibb Company where he is involved in all aspects of primary packaging & device development in the parenteral product development space. Prior to joining BMS, Yusuf was a Senior Engineer with the Materials Science and Technology group at BD Medical. There, he led the design and development of material solutions for various medical products and packaging applications. Yusuf is also involved in academic instruction. He was a visiting professor at the African University of Science and Technology (Nigeria) and the University of New Haven. He currently serves as an Adjunct Faculty in the Biomedical Engineering department at New Jersey Institute of Technology. Yusuf received his Bachelors of Science degree in Chemical Engineering from New Mexico Institute of Mining and Technology and a PhD in Mechanical and Aerospace Engineering (with a concentration in Materials Science) from Princeton University.
2019 - today
Head of Product Management
Seidenader Maschinenbau GmbH, Germany
2015 – 2019
Senior Analyst Strategic Marketing
Körber Medipak Systems AG, Switzerland
2013 – 2015
Master of Science in Business Administration
FH Wedel – University of Applied Science, Germany
Jennifer L. Riter is Senior Director, Analytical Services and Integrated Solutions for West Pharmaceutical Services, Inc., Exton, PA. She joined West in August 1996 as an Associate Chemist in the Quality Control group. Jennifer has held many roles within the West organization and has experience and expertise in several areas from Technical Customer Support, Business Development, Sales and Marketing and Quality. Her most recent role is Senior Director, Analytical Services in the Scientific Affairs and Technical Services organization. Jennifer is responsible for the Analytical Services organization which has four primary areas of focus and thought leadership in Extractables & Leachables, Container Closure Integrity, Packaging and Device/Combination Product Performance and Particle Analysis.
Her experience blends knowledge of West’s components, containment and delivery systems with hands-on experience of providing technical support and analytical solutions for packaging, delivery systems and combination products to West’s multi-national customers. Ms. Riter has also spoken at several symposiums on analytical testing of parenteral packaging components, devices and combination products as well as on extractables and leachables analysis.
Ms. Riter is a member of the Board of Directors for the Lock Haven University Foundation, American Association of Pharmaceutical Scientists, Parenteral Drug Association, and Healthcare Businesswoman Association. She earned a Bachelor of Science Degree in Biology/Chemistry from Lock Haven University, Lock Haven, PA and an MBA in Pharmaceutical Business at the University of the Sciences in Philadelphia, Philadelphia, PA.
Georg Schick is the Strategic Product Manager at Uhlmann Packaging Systems in Germany and therefore responsible for the global strategic product management for Track & Trace. Georg Schick started his career as an electrical design engineer for cartoners and end-of line equipment at Uhlmann in 1999, after he successfully graduated in electrical engineering. A further task he took over was the project management for automation of customized packaging lines. His long-term experience at Uhlmann in various fields of automation and working intensively in projects with customers are the basis for his tasks in sales and product management today. The customers trust in the wide range of Uhlmann products as well as in our experts with fundamental knowledge and that leads to long-term partnerships. One of these reliable experts with the know-how from many customer projects in automation and digitalization is Georg Schick.
Oliver Stauffer received his Bachelors of Science degree from the University of Michigan and completed his MBA at Georgetown University. He began his career in analytical and R & D laboratories, with a focus on sensory technologies, physio-chemical measurement and test method development specific to package testing. Stauffer joined PTI in 2005 as a member of the research and development team working on non-destructive testing of high-risk pharmaceutical packaging. In 2006, he joined the sales team as applications engineer for PTI Inspection Systems. He held the position of International Business Development Manager for PTI through 2010, followed by COO through 2015, focusing on global quality solutions for package inspection that provide the highest level of measurement accuracy and reliability. During his time with PTI he has developed several technology platforms, measurement methodologies, and technology patents. In 2016, he was appointed as CEO.