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Facility Design review for
a new large-scale biopharma and pharmaceutical sites.
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Developed the
integrated timelines
from facility design to product launch for a
major $1 billion Start up.
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Developed and implemented site
project management process.
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Transferred a tabletting
facility from Japan to Ireland.
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Compliance review of Automation
for a large highly automated facility.
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Managed the front-end design of a control system upgrade,
which involved the upgrade of the existing PLC and
batch
control systems
and the integration with the site ERP system.
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Downsized and turned around solid dose
operations for leading
European Pharma Company.
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Rationalised solid dose
manufacturing and packing operations of major generic
manufacturer doubling throughput
in the process
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Re-engineered topical cream & ointment sterile manufacturing
process to reduce the cycle time
from 16 hours to 8 hours
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Undertook process mapping on a medical device manufacturing
facility to convert existing process to
cellular manufacturing and eliminate NVA
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Undertook product development review of powder handling,
granulation and tabletting operations for a large
multinational solid dose manufacturing facility. The
assignment included the redesign of the powder handling and
granulation processes with an
improvement process robustness that saved $1m
annually.
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Designed and implemented a bar code
data collection system to automate inventory
control and dispensing in a paste/tabletting facility.
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Managed and implemented Irish site’s implementation of
corporate enterprise trading system that linked all site
customers to 50+ customers globally. This involved the
refining of processes on site and the
validation of the system to GAMP4
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Facilitated the development of all
Process Designs for an ERP implementation based on
SAP.
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Improved the
Operational Performance
of packaging operations of a Generic Pharmaceutical
Manufacturer
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Re-engineered the assembly
operation for a medical device manufacturer to provide
yield improvements of 25% per batch on
upstream packing operations