Christopher Rasmussen Email and Phone Number
VP of Diagnostics & Bio Device Manufacturing at Zoetis Inc. | Expert in Predictable Factory Operations | Strategic Leader in Pharma Manufacturing at
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Zoetis
Christopher Rasmussen's Location
Lincoln, Nebraska, United States, United States
Christopher Rasmussen's Contact Details
Christopher Rasmussen work email
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Christopher Rasmussen personal email
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Christopher Rasmussen phone numbers
About Christopher Rasmussen
I am a pharmaceutical leader with a passion for helping people live longer and fuller lives. I do this through inspiring others within my organization to deliver the lowest cost and highest quality medicine to our patients. Over the last 25 years I have leveraged my work experience, scientific background and Duke MBA to cultivate a skillset which is broad and agile enough to solve the unique day-to-day and strategic problems facing our regulated industry.
Christopher Rasmussen's Current Company Details
Zoetis
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VP of Diagnostics & Bio Device Manufacturing at Zoetis Inc. | Expert in Predictable Factory Operations | Strategic Leader in Pharma Manufacturing
Christopher Rasmussen Work Experience Details
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Vp Diagnostics & Bio Devices ManufacturingZoetis 2024 - PresentParsippany, Nj, UsLeads all aspects of the Zoetis Diagnostics & Bio Devices global manufacturing and supply operations. Responsible for multiple internal sites located in North Carolina and California as well as Contract Manufacturing operations globally. The Diagnostics & Bio Devices business supports greater than $300 Million in revenue with an exciting growth forecast going forward.
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Vp - Site LeaderZoetis 2021 - 2024Parsippany, Nj, Us• General manager of Zoetis’ largest manufacturing site: 1,000 employees based at two manufacturing sites responsible for the ABI manufacture of monoclonal antibody, bacterial and viral derived antigens; biologics aseptic filling, inspection, lyophilization and packaging; and solid dose, creams and ointments pharmaceutical manufacturing and packaging.• The 1.4 Million ft2 site supplies 1,500 SKUs to >130 countries (supporting >$3 Billion USD revenue).• Successfully manage site through COVID pandemic while mitigating multiple critical material and consumable challenges, while fully removing supply backorders on critical medicines. Built new state of art Monoclonal Antibody facility and transferred, qualified, and registered a novel mAb therapy within the facility.
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Site LeaderPfizer 2019 - 2021New York, New York, Us• General manager of Pfizer’s largest FDA regulated combination product sites: 1,000 employees (Union Workforce) based at two manufacturing sites responsible for the aseptic filling, inspection, assembly and packaging of auto injector combination medical devices. Site is the global supplier of EpiPen (anaphylaxis) and US Department of Defense Auto-injectors (>$1 Billion USD revenue, $225M operating budget).• Responsible for Remediation of a US FDA Warning Letter and Lifesaving Product supply. -
Senior Director, OperationsPfizer 2018 - 2019New York, New York, Us• Responsible for operations at Pfizer’s largest FDA regulated combination product sites: >600 manufacturing, packaging, EHS, transformation, engineering, logistics and procurement employees based at two manufacturing sites.• Cleared the EpiPen drug shortage by implemented Operational Excellence tools to increase Manual Visual Inspection and Assembly & Packaging output by 30% with no capital investments required.
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Operational Excellence & Pmo DirectorPfizer 2018 - 2018New York, New York, Us• Designed and built transformation team from ground up to create a continuous improvement framework for the Pfizer Meridian Medical Technology, Inc. Company: Strategy & KPIs (Design), Business Analytics (Measure), Operational Excellence (Analyze), Program Management Office (Improve), and Integrated Manufacturing Excellence (Control).• Designed and built the site Program Management Office and Process Monitoring and Control programs to support FDA Warning Letter remediation commitments.
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Director Supply Chain OperationsGsk 2017 - 2018Brentford, Middlesex, Gb• Requested by VP Americas and Europe operations to mitigate a business-critical supply chain risk at the Memphis, TN production facility ($185M External (CMO) and Internal revenue).• Redesigned procurement, planning, KPI, warehousing, sales & distribution, and customer relationship management systems; and implemented a SAP ECC6 ERP system to deliver an 80% to 99% OTIF benefit. -
Site LeaderGsk 2015 - 2017Brentford, Middlesex, Gb• General manager of GlaxoSmithKline’s highest volume FDA regulated tableting site: 6-Billion tablets produced annually (120k lbs. of raw materials consumed each day). Site is the global supplier of TUMS (antacid), OsCal (calcium supplement) and Citrucel (fiber laxative) products ($213 Million USD revenue).• Increased the customer service from 35% to 96% through leadership and operational changes.
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Global Logistics Procurement HeadGsk 2012 - 2015Brentford, Middlesex, Gb• Transformed a US and UK based team managing $350 Million in logistics spend into a global organization directly managing over $1 Billion of logistics spend (team of 19 people located in 8-countries).• Delivered a logistics savings benefit of $192 Million over three years through implementation of supplier consolidation, should cost modeling, reverse auction, and supplier relationship management.
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Procurement Commodity DirectorGsk 2011 - 2012Brentford, Middlesex, Gb• Developed and implemented the global GSK green energy strategy and led a team of five commodity managers to deliver high value projects requiring specialized capability and organizational influence.• Designed, developed, and implemented a novel global spend analytics solution capable of aggregating 1.0 Billion GBP in supplier spend across the top 33 global manufacturing sites.
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Procurement Commodity ManagerGsk 2009 - 2011Brentford, Middlesex, Gb• Integrated 42 raw material suppliers into the GSK network during the acquisition of Stiefel Labs.• Mitigated a critical supplier risk by deleveraging and renegotiating a $33 Million raw material supplier contract which was capable of destabilizing $2.96 Billion of annual finished product revenue.
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New Product Introduction Project ManagerGsk 2006 - 2009Brentford, Middlesex, Gb• Managed transfer initiation, pilot and full-scale process development and optimization, process confirmation, validation & information collation, clinical trial supply, through process acceptance and commercial product launch for United States launch of pharmaceutical new chemical entities (NCE).
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Value Stream LeaderGsk 2006 - 2006Brentford, Middlesex, Gb• Led manufacturing operations for PAXIL® and COREG® product families and delivered a 40% reduction in production lead time through implementation of operational excellence tools.
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Validation & Non-Manufacturing Quality LeaderGsk 2005 - 2006Brentford, Middlesex, Gb• Requested by Global Quality SVP to support remediation of the strategically important Cidra manufacturing site under FDA consent decree ($7 Billion in revenue single sourced through factory). • Led a team of 36 people to deliver all FDA validation and systems commitments on-time and in-full.
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Lean Six Sigma Black BeltGsk 2004 - 2005Brentford, Middlesex, Gb• Leveraged Duke MBA experience and lean six sigma training to implement overall equipment effectiveness (OEE), value stream mapping and KAIZEN programs at the Zebulon manufacturing site.
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North America Contract Manufacturing Quality HeadGsk 2001 - 2004Brentford, Middlesex, Gb• Built organization of 21-people and all systems from ground up to provide quality assurance oversight for 20 contract manufacturers and packagers producing product delivering $3.8 Billion in revenue. • Consolidated supplier auditing responsibilities of five North American manufacturing sites into one program which saves GSK $535,000 year-on-year (400 North American suppliers).
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Global Compliance AuditorGsk 1999 - 2001Brentford, Middlesex, Gb• Prepared sites for and facilitated 20 Global FDA inspections in 11 countries across 13 dosage forms; including API, pharmaceutical, biologics and consumer health facilities (all FDA Inspections successful)
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Global Compliance AuditorPfizer 1997 - 1999New York, New York, Us
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Quality Control ChemistPfizer 1995 - 1997New York, New York, Us
Christopher Rasmussen Skills
Gmp
Supply Chain Management
Pharmaceutical Industry
U.s. Food And Drug Administration
Six Sigma
Procurement
General Management
Global Leadership
Global Sourcing
Regulatory Compliance
Quality Assurance
Remediation
Contract Negotiation
Statistical Data Analysis
Lean Six Sigma
New Product Introduction
Technical Transfers
Financial Modeling
Operations Leadership
Compliance Auditing
Quality Auditing
Supplier Relationship Management
Customer Relationship Management
Reverse Auctions
Organizational Design
Monte Carlo Simulation
Decision Trees
Multiple Regession Analysis
Solid Oral Dosage Forms
Logistics Management
Production Planning
Sap Implementation
Project Management
Should Cost Analysis
Project Governance
Quality Systems Design
Quality Control
Value Stream Mapping
Kaizen
Purchase Price Cost Analysis
Sustainability
Warehouse Operations
Organizational Agility
Root Cause Analysis
Problem Solving
Spend Analysis
Contract Manufacturing
Validation
Product Launch
Microsoft Excel
Christopher Rasmussen Education Details
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Duke University - The Fuqua School Of BusinessGeneral Management -
St. Olaf CollegeChemistry
Frequently Asked Questions about Christopher Rasmussen
What company does Christopher Rasmussen work for?
Christopher Rasmussen works for Zoetis
What is Christopher Rasmussen's role at the current company?
Christopher Rasmussen's current role is VP of Diagnostics & Bio Device Manufacturing at Zoetis Inc. | Expert in Predictable Factory Operations | Strategic Leader in Pharma Manufacturing.
What is Christopher Rasmussen's email address?
Christopher Rasmussen's email address is ch****@****gsk.com
What is Christopher Rasmussen's direct phone number?
Christopher Rasmussen's direct phone number is +44-2080-4*****
What schools did Christopher Rasmussen attend?
Christopher Rasmussen attended Duke University - The Fuqua School Of Business, St. Olaf College.
What skills is Christopher Rasmussen known for?
Christopher Rasmussen has skills like Gmp, Supply Chain Management, Pharmaceutical Industry, U.s. Food And Drug Administration, Six Sigma, Procurement, General Management, Global Leadership, Global Sourcing, Regulatory Compliance, Quality Assurance, Remediation.
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