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Massachusetts Institute of Technology

A practical application of simulation for production planning in a flexible pharmaceutical manufacturing environment

Abstract

dc:description.abstract

In pursuit of Novartis Pharmaceutical's vision to "Make Quality Medicine-On Time, Every Time" Novartis Ringaskiddy Limited (NRL), is pursuing Class A Manufacturing (MRP II) certification. Achieving Class A certification requires production plans be established and met with great accuracy. The Multi Synthesis Production Unit (MSPU) at NRL sets rolling eighteen month production commitments on a semi-annual basis. During planning a rudimentary tool is used to allocate production campaigns for over 40 different Active Pharmaceutical Ingredients (API) and intermediate products across roughly 200 pieces of equipment. This manual tool is time intensive to operate, prone to errors, and requires extensive knowledge of the facility. To address this problem, a simulation based model was developed using the software package, SchedulePro". The aim of this project was to create a system to support more effective and reliable production planning. The approach requires accuracy in modeling, a process to deploy the tool and a connection to people who use and benefit from the process. In order to evaluate the proposed model and understand potential benefits to Novartis, five case studies are used to compare the proposed planning process with traditional methods. First, when planning a future production year the proposed planning process demonstrates a reduction in required time as well as an increase in accuracy. Second, when evaluating the response to a change in demand a user with little knowledge of the plant can attain comparable response time as an experienced user of traditional methods. Third, when faced with an unplanned equipment failure the user is able to explore alternative production plans which minimize disturbance to the established production plan. Fourth, through the evaluation of alternative resource allocation plans the user can determine the lowest cost approach. Finally, when applied to a product launch evaluation the model is shown to reduce the number of planning cycles, focusing specifically on the ability of the site to support a product launch in a previously allocated year.

Degree

thesis:*
Department dc:contributor.department
Leaders for Global Operations Program at MIT
Grantor dc:publisher
Massachusetts Institute of Technology
Year dc:date.issued
2014

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Wilson, Christopher J. (Christopher James)
Advisor dc:contributor.advisor
  • Roy Welsch and Charles L. Cooney.

Subjects

dc:subject × 3

Rights

dc:rights
Statement dc:rights
  • M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.
Language dc:language.iso
eng

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/1721.1/90750
OAI identifier oai:identifier
oai:dspace.mit.edu:1721.1/90750

Chain of custody

source
Harvested from
MIT
Base URL
dspace.mit.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Wilson, Christopher J. (Christopher James). A practical application of simulation for production planning in a flexible pharmaceutical manufacturing environment. Massachusetts Institute of Technology, 2014. http://hdl.handle.net/1721.1/90750