From tackling personal decisions to reaching important milestones, my job is to guide you on the path of success.
I have over 26 years of experience as a leader, engineer, and executive in the highly regulated industries of pharmaceuticals and medical devices. My wide range of experiences include facilities, construction, manufacturing, logistics, maintenance, safety, and IT. My extensive experience with FDA and EU regulators, as well as responsibilities for launching numerous products, can help your company on a wide variety of projects.
I am one of just over 100 professionals worldwide that have been certified by the International Society of Pharmaceutical Engineers as a Certified Pharmaceutical Industry Professional (CPIP).
To be eligible, you’re required to have a valid science or engineering degree and/or 10 years of industry experience and the program itself has rigor. It mandates that participants exhibit knowledge and skills in areas such as leadership, change management, quality and continuous improvement, as well as technical knowledge in seven categories:
1. Product development
2. Facilities and equipment
3. Information systems
4. Supply chain management
5. Production systems
6. Regulatory compliance (includes drugs, EH&S)
7. Quality systems
Additionally, JW Consulting Engineers has access to a consortium of other Life Sciences consultants and Engineers with experience in other areas such as computer systems validation, regulatory, safety, quality and project management. This consortium is working together to give their clients a “one stop shop” for all of their consulting needs.
Brief Resume` (reverse chronology)
Principal Consultant, JW Consulting Engineers
Vice President/Principal, GBA
VP Manufacturing—Atrix Labs/QLT USA/TOLMAR
Facilities Site Manager—Gambro BCT
Facility Engineering Manager— Geneva Pharmaceuticals
Maintenance Supervisor—Sundstrand Aerospace
US Naval Officer
Get in touch with me today for a consultation.