Meet the Speakers

Anna Thomas

Associate Manager of Packaging


Anna is currently the Associate Manager of Packaging at SeaSpine, a spinal medical device company based out of Carlsbad, CA. She graduated from Michigan State University in 2017 with a degree in Packaging and a minor in Environmental and Sustainability Studies, where her passion and eagerness to learn about sustainability sparked. Prior to joining SeaSpine, she worked for 3 years as a Packaging Engineer at NuVasive, as larger spinal medical device company also based out of Southern California. Over the course of the past 6 years, Anna has made it a priority to spend time working with purchasing, supply chain, distribution, sales, and nurses in the field to understand the “big picture” of how SeaSpine’s products get packaged, and where sustainability can make an impact. She still performs the day-to-day job of a typical packaging engineer (design, development, testing, and implementation), but whenever there is spare time, Anna is eager to implement sustainable practices within her work. Being at a smaller medical device company has given Anna the opportunity to integrate herself into understanding the complex supply chain of “loaner set” style Orthopedics. Anna is determined to use her knowledge of the time and energy it takes to get a single use product packaged and to the market to influence other early life or end of life teams at SeaSpine, and long term, in the market overall.

Arti Roth, Ph.D.

Senior Engineering Manager

Edwards Lifesciences

Arti leads the Advanced Packaging Technology team at Edwards Lifesciences. She transformed and built a group that is focused on delivering high value packaging solutions. Her team focuses on a diverse array of difficult solutions encompassing novel designs, predictive engineering, sensors, track & trace systems, usability, and sustainable materials.

Arti believes in the power of creativity to make a positive impact on society. Her diverse breadth of experience includes developing high speed semiconductor chips and optical gas sensors for NASA. As a postdoctoral fellow at ETH Zurich, she developed femtosecond lasers using engineered semiconductor materials that she developed and characterized for her PhD work at UC Berkeley.

In her free time, Arti enjoys time with family and friends and playing board games.

Austin Liu

Senior Package Engineer

Johnson & Johnson Surgical Vision

Austin Liu is Senior Package Engineer at Johnson & Johnson Surgical Vision in Irvine, California. He acts as Secretary of The Last 100 Yards (L100) Program of the Kilmer Innovations in Packaging (KiiP) organization and is actively managing several Institute of Packaging Professional (IoPP) Medical Device Packaging Technical Committee (MDPTC) Programs. He holds a BS in Packaging from Michigan State University and has served the healthcare packaging industry through Test Laboratory, Consulting and Contract Manufacturing Organization (CMO) capacities for the past 4+ years.

Brian Farison

Technical Fellow

Network Partners

Brian Farison is Technical Fellow with Network Partners with over 38 years combined experience in packaging, medical devices and process excellence. His career expertise spans the areas of structural and medical package design, process development and validation, Six Sigma and Lean process improvement, project management, quality and compliance, risk mitigation and deployment of strategic high-visibility projects and initiatives. Brian is a published author, conference speaker, and member of ASQ and ASTM. He holds seven US Patents and multiple Worldstar and Ameristar package design awards. He is a Certified Six Sigma Master Black Belt, Certified Packaging Professional-Lifetime with IoPP, and award-winning member of Toastmasters Int’l.

Chris Kelley

R&D Packaging Engineer


Chris Kelley is the sole R&D Packaging Engineer supporting Coloplast’s Interventional Urology division in Minneapolis, Minnesota. With previous experiences in both test laboratory and medical device manufacturer R&D settings, Chris is dedicated to improving patient safety through sterile barrier packaging design and testing while promoting the core value of the Coloplast business: “serving individuals with intimate healthcare needs”. Holding a BS in Packaging, from the University of Wisconsin Stout as of May of 2021, he remains active in the packaging community that has helped expedite his professional career. He participates in local Institute of Packaging Professionals (IoPP) MN-Chapter networking/charity events, and co-leads the IoPP’s national-reaching Medical Device Packaging Technical Committee’s (MDPTC) Coaching Program which encourages career development and technical knowledge sharing for new engineers in the Medical Device Packaging industry.

Cliff Labbe

 Director of Package Development

Johnson & Johnson

Cliff Labbe is the Director of Package Development in the Johnson and Johnson MedTech Sector. He has over 20 years’ experience in materials science and package development including roles at Cymetech and Alcan in his career. Cliff’s team has the responsibility of designing and developing packaging solutions for sterile single use devices and capital equipment. He is passionate about developing his teams’ strengths and enabling them to connect problems with solutions through creative engineering. Cliff loves the outdoors and spending time hiking with his family. That hobby has fueled his passion in sustainability and in reshaping the packaging industry’s impact on the environment.

Cristina Indiveri, MS

Associate Vice President of Core Tenets


Cristina Indiveri, MS is Associate Vice President of Core Tenets at Vizient. In this role, Cristina guides the strategy of Vizient’s industry leading Environmental Sustainability Program which sets the standard for reducing our provider’s environmental impact while empowering smart, sustainable, resilient choices. In addition, Cristina provides strategic and operational leadership for Novaplus, the industry’s longest-running private label program, Vizient’s Domestic Sourcing initiative which identifies domestically manufactured products to bolster continuity plans and Vizient’s Pediatric Program which provides an exclusive product portfolio of pediatric medical supplies and equipment.

With approximately 15 years of experience, she has held various leadership roles in healthcare. Prior to joining Vizient, Cristina led a number of support departments and programs including sustainability at Yale-New Haven Hospital, a 1,541 bed non-profit medical center in New Haven, CT. Cristina holds a Master of Science degree in Health Systems Administration from Georgetown University and lives outside of Dallas with her husband, two children, and two huskies.

David DiVaccaro

Packaging Consultant

DiVaccaro Consulting Group

David DiVaccaro is a 6-sigma Certified Process Excellence Black Belt with his bachelor and master’s degrees in Packaging from Michigan State University. He has served as Ombudsman for IoPP’s Medical Device Packaging Technical Committee for over 11 years. He has worked in the Medical Device and Pharmaceutical industries for over 30 years with companies such as Edwards Lifesciences, Zimmer Biomet, Johnson & Johnson-DePuySynthes, Sanofi, Johnson & Johnson-Cordis, Baxter, and various start-ups. He has expertise in Package Design, Process Validation, Machinery Selection/Replacement, Package Risk Assessments, Remediation, and Supplier Relationships.

He has demonstrated success as a consultant, team leader, team member, as well as an Individual Contributor.  Former designs have earned 2 Ameristar Awards. Contributing author for The Medical Device Validation Handbook (1st and 2nd editions), Moderator thePACKout 2022 – “Unpacking Human Factors/Usability Engineering w/ Live Simulation”, Speaker at HealthPack 2018, 6 Steps to Successful Remediation, Panel Member at HealthPack 2019, ORTHOWORLD, BONEZONE March 2018, Interviewee, Vital Validation Considerations for Your Next Packaging Project. He is a long-term member of IoPP, former VP and co-founder of the South Florida Chapter, and former member of Drug & Pharmaceutical Packaging Committee. Member ASTM. Since 2013 he has been consulting with Medical Device firms as part of DiVaccaro Consulting Group, LLC.

David Grosse-Wentrup

Research Director

Design Science

David Grosse-Wentrup is the Research Director at Design Science, a global human factors consultancy focused on advancing healthcare technology through user research and design evaluation.

After his studies in biomedical engineering and postgraduate research at the faculty of medicine at the University of Münster, Germany, as well as work for the Centre for Global eHealth Innovation, Toronto, Canada, and GE Healthcare, Wuxi, China, he joined Design Science’s U.S. office in 2016.

At Design Science, David and his team are supporting clients in evaluating, improving, and obtaining approval for medical devices and combination products for the U.S. and EU market. He is currently leading efforts to opening Design Science’s first European office in Munich, Germany.

Deepa Rampura

Manager, Packaging Engineering

Intuitive Surgical


Dr. Megan Frost

Chief Technology Officer

Sterile State

Dr. Megan C. Frost is the Chief Technology Officer for Sterile State. Dr. Frost has worked on the development of medical polymers and their applications to devices for over 20 years. She earned a BS in Biological Sciences from the University of Notre Dame, a BS in Chemistry with a minor in Mathematics and an MS in Analytical Chemistry from Purdue University – Indianapolis, and a PhD in Chemistry with a Graduate Certificate in Cellular Biotechnology from the University of Michigan – Ann Arbor. She was a post-doctoral researcher in the Department of Surgery at the University of Michigan Medical School. Industrial experience gained prior to completion of graduate studies includes working at Dow Elanco (Indianapolis, IN) in the Technology Applications Group. Dr. Frost also has experience as an analytical chemist at Eli Lilly and Company (Indianapolis, IN).

Hanna Harris

Senior Design Engineer

Healthmark Industries

Hanna Harris is a Senior Design Engineer at Healthmark Industries, a global provider of solutions that aid in the delivery of surgical instruments and lifesaving medical devices. After starting her career in medical packaging, Hanna quickly grew passionate about ensuring product and patient safety through packaging solutions. Leveraging her diverse background in package design, regulatory requirements, and product development, she focuses on a user centered approach to drive packaging innovations. Hanna is active in initiatives to promote industry development within Kilmer Innovations in Packaging (KiiP) and the Medical Device Packaging Technical Committee (MDPTC) of the Institute of Packaging Professionals (IoPP).

Jamie Pero Parker, PhD

Sustainability Sector Lead

RTI Innovation Advisor

Jamie Pero Parker, Ph.D. is the sustainability sector lead for RTI Innovation Advisor, an innovation consultancy housed within RTI International, a global not-for-profit research institute.  Jamie has been with RTI Innovation Advisors for 13 years and has advised many of the world’s leading companies on circular plastics, sustainable packaging, green chemistry, and the emerging circular economy.  She has also written about how sustainability changes the innovation process and has collaborated or supported various consortiums in the space.  


Prior to her work at RTI International, Dr. Pero Parker was a scientist with The Clorox Company. Her published works include: 

  • From waste to value: Business opportunities in solid waste management
  • Defining sustainability and how it changes the innovation process, printed in Sustainability and eco-responsibility: Advances in the cosmetic industry
  • A maturity model for sustainability in new product development
  • How Sustainability Changes the Innovation Process
  • Practical Insights into Open Innovation for Sustainability 


Dr. Pero Parker holds a Ph.D. in analytical chemistry from the University of North Carolina at Chapel Hill.

Jan Gates

President / Advisor Packaging Engineer

Adept Group

Jan Gates has 35+ years of experience in package engineering for foods, pharmaceuticals, detergents, and medical devices, with a BS in Food Science and MS in Packaging from Michigan State University. Her work includes individual contributions and leading departments for packaging material and systems design and development to meet regulatory, product protection, and customer use requirements. Her work also includes production optimization, validation, and minimal packaging for sustainability, with cost reductions always in mind. Jan is a member of ASTM D10 and F02 committees for rigid/flexible packaging and environmental package testing. She also serves as a US representative on various ISO TC 122 committees for packaging testing, labeling, and product shipment. She has been a member of IoPP (Institute of Packaging Professionals) since before it was called IoPP and is an IoPP Medical Device Packaging Technical Committee member. She previously worked for Bristol Myers Squib, Conagra, Lever Brothers, Dade Behring, Abbott Vascular, PackWise Consulting, and Adept Group.

Jen Benolken

MDM & Regulatory Specialist, Packaging Engineering, Tyvek®, Medical Packaging


Jen has worked in the medical device community since 1991 in a variety of packaging roles – packaging, labeling, and sterilization engineer in operations and R&D, flexible packaging sales representative, and manager of packaging engineering and labeling groups. She is currently the sub-committee chairperson for ASTM F02.50, Package Design and Development, as well as co-chair for AAMI’s ST/WG 7, Packaging Working Group. Jen is an active member of the Institute of Packaging Professionals (IoPP) where she attained her lifetime Certified Packaging Professional (CPPL) certification in 2012. She is also on its Board of Directors and is Chair on its Medical Device Packaging Technical Committee (MDPTC). Jen is also a founder of and chairs KiiP (Kilmer Innovations in Packaging), an industry led group of packaging professionals interested in driving innovation through collaboration in the sterility assurance value chain. Jennifer is the editor for the upcoming 3rd edition of the Medical Device Packaging Handbook. She works with downstream customers at medical device and pharmaceutical organizations, providing education and answering questions about Tyvek® packaging and sterilization using her wide range of knowledge.

Katherine Hofmann, PhD

Sustainability Strategic Initiatives Manager


Katherine Hofmann earned her BS in polymer science engineering from Case Western Reserve University and her PhD from Virginia Tech in 2012 performing research on novel fuel cell membranes with General Motors. After completing her degree, Katherine joined Eastman in 2012 as part of the Polymers Technology Division working in front end research, product development, and applications development. During this time, she helped launch Tritan Renew, Eastman’s first molecularly recycled material, and leveraged her expertise in ISCC+ certification to assist customers across multiple industries to successfully achieve certification. In the summer of 2022, Katherine joined Eastman’s corporate sustainability team as a Sustainability Strategic Initiatives Manager supporting Eastman’s Plastics and Coatings and Inks businesses. In her current role, Katherine helps drive sustainability efforts and strategy within the organization as well as helps advance the adoption of molecular recycling externally with customers and across the value chain. Katherine actively invests in the medical plastics community through education and project leadership in organizations such as Kilmer Innovations in Packaging (KiiP) and the Healthcare Plastics Recycling Council (HPRC).

Keith Weitz

Director of the Sustainability and Resource Management Program

RTI International

Keith A. Weitz is the Director of the Sustainability and Resource Management program at RTI International, a global not-for-profit research institute. Mr. Weitz specializes in the development of data, methods, and decision support tools to support public and private sector decision makers as they grapple with waste and material management challenges. His experience in the management of medical waste sector combines life-cycle environmental assessment with economic and social impact assessments to provide a more complete evaluation of sustainability. Mr. Weitz is currently leading research to identify interventions to improve the recovery and recycling of municipal and medical waste, reusable medical device and packaging, and to characterize the technical, economic, and environmental potential for new and emerging material management technologies to enhance recycling. Mr. Weitz holds a Master of Environmental Management from Duke University and a B.A. in Economics and Business Administration from Augustana College.

Ken Karpiloff

Principal Packaging Engineer

Adept Group

Ken Karpiloff has 35+ experience in package engineering for industrial products, food, pharmaceuticals, cosmetics, alcoholic beverages, cold chain, and medical devices, with a BS in Industrial Engineering from Hofstra University. His work includes individual contributions and leading departments for packaging and production, including developing packaging materials, packaging processes, packaging equipment, and systems design and development. The packaging design and development have been completed to meet regulatory, product protection, and customer use requirements. His work also includes production optimization, validation, and the right packaging for sustainability, with a specialty for cost reductions, problem-solving and doing right the first time. He previously worked for Becton Dickinson, Guinness/Diageo, Avon, Revlon, Shiseido, Duracell and is currently with the Adept Group

Kurt Yockey


Kurt Yockey has worked extensively with physicians, hospitals, medical product manufacturers, and other healthcare professionals and entities for over 40 years. He is preferred counsel in complex litigation involving employment matters, orthopedic surgery, emergency medicine, obstetrics and cardiology, and medical device matters. Kurt has been general counsel for innovative medical product development companies including Zip Pak Inc., J.M. Longyear, Pioneer Surgical, Frontier Medical Products, Samaritan Medical and Sterile Spaces LLC. In 2005, Kurt was named a Michigan “Lawyer of the Year” by Michigan Lawyers Weekly for his role as hospital counsel in finding a defect in a medical device, leading to the manufacturer making a design change which avoided patient injury. He is AV rated by Martindale-Hubble. He received his undergraduate degree from Michigan State University in 1977 and graduated with honors from the Detroit College of Law in 1981. He has been a member of the State Bar of Michigan since 1981, and has been admitted Pro Hac Vice to handle matters in Ohio, Maryland, Texas, Oregon, Washington, Illinois, California, and Florida. Mr. Yockey has served as a panel member of the Attorney Discipline Board since 1988.

Lisa McTigue Pierce

Executive Editor

Packaging Digest

Lisa McTigue Pierce is Executive Editor of Packaging Digest“The Voice of the Packaging Community.” She has been a packaging media journalist since 1982 and has worked on several different packaging publications during her career, including as Editor-in-Chief of Food & Drug Packaging. In her current role, Pierce tracks emerging trends, new technologies, and best practices across a spectrum of markets for the publication’s global community.

Mathias Romacker

Executive Advisor


Mathias Romacker has more than 30 years of experience in injectable drug-delivery devices on the pharmaceutical and packaging supplier sides. Romacker joined Kymanox as an Executive Advisor in October 2022, where he is part of a team of seasoned former executives who share their experience and insights with pharmaceutical and medical device companies. Previously, he was Principal of Romacker Injection Device Strategy LLC, having retired from corporate life in December 2019. As a consultant, he stayed connected to the industry through speaking engagements and in advisory roles. And in January 2020, he joined the Board of Directors of the Parenteral Drug Association (PDA).


He has held various executive positions at various manufacturers, lastly as Senior Director, Device Strategy, for Pfizer, at its headquarters in New York City. He joined Pfizer in March 2015. In this role within Pfizer Global Supply, Romacker focused on the front end of device technology. He worked with multiple functions and sites across the organization to develop a device strategy for Pfizer’s pipeline and inline products. Before that, Romacker held positions in sales and marketing, as well as in operations at Becton Dickinson (BD), Gerresheimer, and Amgen. He has extensive international experience from his positions in the US, Germany, and South Africa, in both domestic and global positions. Romacker has a solid understanding of the markets for pre-filled syringes, handheld injection devices, and wearable devices. He has been involved in multiple successful product launches with combination products. In addition, he has chaired many high-profile industry conferences focused on the increasing interest in device technology and the need to differentiate drug products and enhance patient adherence. Romacker was the co-chair for PDA conferences “Universe of Pre-filled Syringes and Injection Devices” in Basel in 2013, Vienna in 2017, and in Gothenburg, Sweden, in 2019. In 2018, the PDA awarded him the “Edward Smith Packaging Science Award” for his contributions over the years. Romacker holds the equivalent of a master’s degree in economics from the University of Freiburg, Germany.

Matt TerBush

Senior Laboratory Packaging Engineer

Packaging Compliance Labs 

Matt TerBush serves as the Senior Laboratory Packaging Engineer at Packaging Compliance Labs (PCL) within the Innovations Department. Matt has over 8 years of experience in packaging engineering. By leveraging his packaging engineering knowledge, Matt served as the Director of Operations for PCL for 4 years. He led key initiatives for growth within the laboratory and created the foundation for all of PCL’s current testing offerings. Through this process he became intimately involved in lab operations and developed into his current role as he discovered an opportunity to enhance the harmonization between lab procedures and engineering. Matt also serves as PCL’s leader within the Usability program for being data driven and an expert within ISO 11607, Section 7 as well as serves as PCL’s ear to the industry by serving on the ASTM F02 and D10 committees. 

Michael Johnston

Packaging Engineer

MicroAire Surgical Instruments

Michael Johnston is a Packaging Engineer for MicroAire Surgical Instruments located in Charlottesville, VA.  Michael attended the University of Wisconsin, Stout in Menomonie, WI where he majored in Packaging and minored in Business Administration.  When he was 13 years old, Michael was diagnosed with a cancerous brain tumor.  While in the hospital, Michael experienced several different types of packaging and was fascinated with the packaging.  After learning more about packaging in general, he made it his goal to become a packaging engineer to improve the packaging that he encountered while in the hospital, not just for the hospital staff, but for the patients as well.  Michael is now in remission and he wants to use his experiences to bring industry awareness to the observations he made about the medical packaging he encountered and hopes that the industry will think of the patient when designing packaging, not just the end user.

Nancy Battaglini

Sr. Principal Packaging Engineer


Nancy Battaglini is the Sr. Principal Packaging Engineer supporting Medtronic’s Sustainability Development Center. She has over 13 years of packaging experience in the consumer goods, food, and medical device industries. Throughout her career, Nancy has been focused on sustainability driven initiatives through material reductions, implementing alternate structures, and improving packaging footprints across these industries. She is currently focused on driving Medtronic’s externally facing Sustainability goals of reducing packaging and paper waste. Nancy actively participates in employee resource groups within Medtronic and enjoys coaching aspiring technical leaders. Outside of work, Nancy is an avid yogi and rock climber and enjoys spending time with her spouse and 2 fur babies.

Nick Packet

Healthcare Industry Vertical Manager


Nick joined the medical device industry in 2004 as a packaging engineer at Boston Scientific. He worked as an engineer for several years and had the opportunity to lead a packaging team in 2013. During his time as an engineer, he gained a wide range of experience in package development, testing, and process qualification. In 2017 Nick joined the DuPont™ Tyvek® healthcare team supporting medical device manufacturers, and in August of 2022 he moved to his current role as the Tyvek® Healthcare Industry Vertical Manager. With a broad perspective of the market, he strives to provide technical support, insights on sustainability, and works across the value chain to identify opportunities that demonstrate how packaging can play a positive role in the lifecycle of a product. Active in industry groups, Nick has had the opportunity to join and lead projects and efforts within the Healthcare Plastics Recycling Council (HPRC), Kilmer innovation in Packaging (KiiP), and the Sterilization Packaging Manufacturers Council.

Nora Crivello

President & CEO


As the President & CEO of Westpak, Nora Crivello leads of team of over 85 at two locations in Northern and Southern California. Westpak is an independent and accredited testing laboratory serving a variety of industries in product and package validation work. Through her 20 years at Westpak, she has been “boots on the ground” as a Test Engineer, Quality Manager and Vice President, making her uniquely qualified to now serve as the CEO. Nora is also the Vice Chairman of the ISTA Board of Directors and sits on numerous industry committees including Kilmer Innovations and ASTM. Nora holds a BS from California Lutheran University and an MBA from Pepperdine. Outside of Westpak, Nora’s volunteerism and Board involvement revolves around promotion of educational opportunities for women and disadvantaged communities. She lives near the Central California coast with her husband and two teenagers and enjoys any activity involving the outdoors and National Parks. Together, the family raises guide dog puppies for Guide Dogs for the Blind.

Paul Nowak

Executive Director


Paul Nowak, the Executive Director of GreenBlue, brings 30+ years of experience to the table through a variety of roles across the supply chain including, vice president of sustainability at Quad, general manager of manufacturing, senior director of client experience, and vice president of enterprise solutions for brands. Nowak’s passion for sustainability and embodiment of GreenBlue’s core pillars are demonstrated through his career accomplishments, including the creation of the first Quad Sustainable Packaging Public Report, the Annual Client Sustainability Symposium, and the development of the Quad Community Education Program. During his career, Nowak has highlighted the importance of diversity and inclusion in the industry by serving as a diversity, equity, and inclusion (DEI) leader, founding the first Quad Business Resource Group for LGBTQIA+ teammates.

Peylina Chu, PE

Senior Vice President, ESG Business Strategy

Antea Group

Peylina Chu is a master at helping companies manage the multiple business aspects of ESG and Sustainability, from materiality to stakeholder engagement, to strategic investment for business value and positive impact. With her 20+ years of experience, she understands that in addition to traditional regulatory drivers, today’s companies must meet public and customer expectations, investor concerns and non-governmental organization demands. Peylina leads the Healthcare Plastics Recycling Council (HPRC), a private technical consortium of industry peers across the manufacturing, healthcare, and recycling industries seeking to improve the recyclability of plastic products and packaging used within healthcare.

Rod Patch

Senior Director, Package Engineering

Johnson & Johnson Vision

Rod Patch, Senior Director, Package Engineering, Product Labeling & Digital Product Information at Johnson & Johnson Vision. Rod has led package engineering and product labeling teams in multiple J&J MedTech businesses spanning joint reconstruction, spine, trauma, sports medicine, cardiovascular, electrophysiology, gynecology, ENT, bariatric, biosurgery, energy, endo-mechanical, wound closure, breast reconstruction, and now surgical vision and vision care solutions.

Rod is a graduate of Michigan State University School of Packaging with an MBA from Regis University. Rod is a designated US Expert for ISO / AAMI Technical Committee 198, Working Group 7, primary J&J voting member in ASTM F02/D10, a member of IoPP Medical Device Packaging Technical Committee (MDPTC), a founding member and Vice Chair of Kilmer Innovations in Packaging (KiiP), and a Founding Expert for the[PACK]out™ Conference.

Samantha Smith

Director of Product Stewardship


Samantha Smith has 20 years of packaging design and development experience with companies such as Medtronic, Schick, BIC, P&G, and Honeywell. Samantha has also led packaging design teams, as well a test lab. She spent 4 years in Procurement leading the packaging category strategy for Medtronic.

Currently Samantha is the Director of Medtronic’s newly created Sustainability Design Center. In this role she is responsible for supporting the Medtronic Sustainable design projects that directly impact the published packaging and IFU reduction goals.

Samantha received her B.S. in Packaging from Michigan State University.

Seema Momin

Global Account Manager


Seema Momin, CPP is a Global Account Manager at PAXXUS, a vertically integrated manufacturer and provider of flexible barrier packaging products to medical device, pharmaceutical, and diagnostic companies. Prior to this role, she had 3 years of packaging engineering experience in the healthcare industry, and worked with Class I, Class II, and Class III medical devices, combination products, and various temperature sensitive pharmaceuticals. She has experience leading design verification projects, process validations, stability studies, test method validations, remediation projects and supporting CAPAs and large-scale site transfer projects. Seema earned her undergraduate degree in Packaging from Michigan State University. She serves as the Events Chairperson of IoPP’s Medical Device Packaging Technical Committee (MDPTC) and is part of the Membership Committee for Kilmer Innovations in Packaging (KiiP).