Thomas J Tsilionis, Pmp Email & Phone Number

Teaneck, New Jersey, Us

Consultant / GSK Smart Manufacturing Scheme Design:Consultant for the ‘Connected Worker’ Platform, as part of GSK's digital transformation program. Conducted workshops at client US site, interviewing manufacturing roles to establish ‘persona journeys’ and usage of IT/OT systems, identified gaps & opportunities, and helped develop use-cases. Technologies included ‘Guided Execution’, ‘Augmented Reality (AR)’, ‘Zero-Touch’, ‘Smart Training’, & ‘AI-enabled Digital Coach’.Team Leader-AbbVie Cyber-Attack Resiliency Program:Technical Team Leader on a Cyber-Security / Cyber-Resiliency Program for client AbbVie Pharmaceuticals, which provides a framework for disconnected plants to operate for long periods of time if disconnected from the Enterprise, and also facilitates recovery and remediation of systems within the MCN after a cyber attack.

Principal/Owner and Independent Consultant providing Engineering and IT Project Management, Industrial Automation Systems, Software Integration, and System Validation consulting services for Pharmaceutical and Consumer Products Industries. Key Clients served:NOVARTISContracted (through Insight Global) to be a Sr. IT Project Leader at Novartis in East Hanover NJ, in the Development IT group. Responsible for successfully leading three software application release deployments for the company wide document management system, over a span of almost 2 years. Responsible for interfacing, collaborating, and coordinating with a matrix of teams and management levels, managing scope, resources, timeline, and deliverables. PFIZER, INC.: Provided IT Project Management services in the Legal BT group on multiple work streams that included several enhancements to TeamConnect, development of requirements/workflow for Digital Media Governance web portal, focusing and managing implementation of Remote Access tools for external vendor, and server retirement.ACTAVIS PHARMACEUTICALS: Successfully Project Managed dozens of engineering projects for generic Pharma client (Actavis), over 5 facilities, including 3 new hi-speed packaging lines, purified water systems, compressed air systems, dust collector systems, pan coating machine & air handler, granulated powder drying ovens, QA Sampling Booths, gowning rooms, water mixing stations, and facility equipment/hardware/signage. Developed dozens of User Requirement Specifications, commissioning documents, and change controls.

I joined Actavis in May of 2013, as part of Global Engineering at Actavis Corporate headquarters in Parsippany, supporting multiple packaging sites, both US and overseas. Successfully managed multiple new packaging line implementations ($6 million, solid oral dose bottling), and packaging line equipment upgrades (cartoning and bottling), and serialization program line implementations, globally. Actavis became Allergan, and then Allergan sold off the Actavis generics business to Teva Pharmaceuticals. I became a Teva employee as part of that deal .As of the August 2016, I became part of Teva, and my role became focused on being the Americas Regional Lead for the TEVA Global Serialization Program, overseeing serialization program activities for packaging line implementations at multiple sites and on multiple packaging lines, to meet the US regulatory compliance deadline for serialization by November 2017 (which was then moved to Nov 2018 enforcement date). My role also included actively managing selected vendors, tracking of costs and timelines, developing corporate standards, and harmonizing sites to follow standards and common practices. The Serialization deadline for the US was successfully met without any significant issues nor downtime across all sites supplying the US market. In additional , my oversight included 2 EU sites that met their compliance date for FMD requirements for Feb 2019. Total scope of oversight was 89 lines, 15 sites, $43 mil, all successfully implemented with no disruption.Next phases of serialization included overseeing lines to prepare for supply to the Russia market (2020), and also the Aggregation requirement for the US Market (2023). Participated in the development/selection process of vendors, sites, and lines for the Aggregation Pilot project.

New Brunswick, Nj, Us

Post purchase of Pfizer Parsippany Site by J&J, was Site leadership for Automation and Telecommunications, in addition to IT application support (Crystal Reports, Calibration Manager), and supporting site closure activities including transfer of product lines to other J&J facilities and disposition of equipment and accounts as employees were released from the site.

New York, New York, Us

Site Automation Lead at a Manufacturing Site, leading several major projects, key strategist, standards developer, GMP compliance validation, site controls support, IT systems support. Member of 21 CFR Part 11 Team and Right 1st Time (Six Sigma) Team. Managed and implemented projects including packaging lines, manufacturing batch, facilities & environmental, IT systems, MES initiative, automation LAN, Data Historian, and infrastructure for the Parsippany, NJ manufacturing plant.

Lead project engineer and developer for multi-industry systems integrator. Project management, engineering and development for projects in various industries. Projects included packaging lines, batch manufacturing, purified water and treatment systems, and recipe systems, spanning Pharma, Consumer Products, Cosmetics, Beverage, Flavors, Petroleum, Chemical, Steel, and Cement industries. Major clients included Johnson & Johnson, Pfizer, Hoffman-La Roche, Carter-Wallace, Lipton, and Pepsi.

Electrical and Controls Systems Design, Implementation and Project Engineering for Material Handling Systems (UPS, FEDEX, RPS) and Baggage Handling Systems.

Mba, E-Commerce & Technology Mgmt

Bsee, Electrical Engineering / Maj: Digital Circuit Design