HCi Journal of Information Development

The manager, his assistant, the QA manager, the accountant, and the multi-national analyst

By Onno van Ewyk

This is the true story of a transformation that took place in the manufacturing operation of a multi-national pharmaceutical company. This transformation took it from being an efficient, well-run, and people-centric operation to an even more efficient and better-run people-centric operation.

It is a story with happy beginnings but a sad ending. There are two heroes - a recently appointed young manufacturing manager and his assistant - and three villains - the QA manager, an accountant, and a multi-national strategist.

Under threat

The story begins when the manufacturing manager and his assistant decide to radically upgrade the way they manage the operation. Although the plant was already running efficiently by world standards using traditional conservative bureaucratic methods (including a benevolent and supportive attitude to staff), it was under threat of closure because of a world-wide rationalisation of manufacturing operations that was taking place.

The manager and his assistant felt that the best way for them to respond to this challenge was to make their plant not only good, but the best in the world. They planned to do this by introducing a continuous improvement approach that bolstered teamwork and encouraged creativity moderated by disciplined measurement and analysis. The aim was not to overturn or replace what they were currently doing, which was working well enough, but to boost it and if possible raise performance to a higher level.

Designing the program

The manager engaged a consultant to help design a program for introducing the new approach. They decided to group the staff into ‘natural work teams’, that is, those who performed particular functions together, and to appoint team leaders from the supervisor-level staff. This meant that the new approach would align, and therefore not conflict, with existing authority and organisational reporting lines. Time was set aside during regular working hours for the teams to meet and discuss how their teams were performing and how they would make improvements.

Having set up this operating framework, a training program was designed and implemented to give the staff the necessary skills. All 50 staff members attended two days of training, which covered small-group skills (teamworking), analytical methods (customer supplier mapping, flowcharting, pareto analysis, cause and effect diagrams, statistical process control) and creativity tools (nominal group technique, brainstorming).

The manager decided that the program should have a name, so it was called SCIP. The S stood for the company name, let’s call it Summer Pharceuticals, and the CIP for Continuous Improvement Program.

From the outset, the QA manager was involved in the program. The manufacturing manager and the consultant argued that quality assurance could only benefit from the program because it would focus all staff in a direct and practical way on quality issues. Outwardly the QA manager agreed, but it subsequently became apparent that his support was not whole-hearted.

The teams

After the training, the teams began their work in earnest. They met, talked, analysed, agreed, and acted. Not everyone displayed the same level of keen-ness and commitment. Each SCIP team comprised 6-7 people. Of these, typically, there was:

Even with this level of participation, which could be expected to improve as team leaders grew more skilled over time, the impact of the SCIP teams was immediate and impressive. It is worth looking in detail at some of the things they achieved during the first year.

The buckets

The output of the tablet compression machine had always been collected in 18 Kg plastic buckets. These were heavy and awkward to handle, particularly for the women who comprised most of the workforce in the area. These buckets could not be lifted up to the hopper of the packaging machine. This hopper was so high off the ground it required a step ladder to reach it. As a result, tablets had to be transferred using a scoop. This was slow and often caused damage to the tablets, which were easy to chip or break.

Another problem was that the bucket size had naturally become the de-facto unit of measurement for production runs. This meant that smaller packaging runs were often wrongly estimated, requiring already packaged tablets to be unpacked and repacked in other boxes to satisfy orders.

The SCIP team involved with this process examined the problems and proposed that 10 Kg buckets be used instead. They put their arguments to management, who agreed and gave their approval to replace the buckets. This cost less than a thousand dollars.

The packaging operation was speeded up (no precise measurements were taken because the advantages were so obvious), damage to tablets dropped to virtually nil, there was now a significantly lower risk of injury to workers handling the buckets, and smaller packaging orders were now consistently accurately filled.

There was an unexpected benefit after the smaller buckets began to be used. Each bucket was normally weighed after filling from the compression machine. A metal detector on the compression machine required a minimum drop distance. The smaller bucket allowed the weighing machine or balance to be placed under the bucket. Previously the larger bucket had to be transferred to the balance after filling. With the smaller bucket being filled on the balance, handling was reduced and workers were able to fill each bucket with a consistent weight of tablets.

Dust extraction

The plant had a new dispensary for ingredients that was fitted with high volume dust extraction in order the keep the air clean. The system was so efficient it was extracting 500 Kg of raw material each year, worth $10,000. The SCIP team achieved a 60-70% reduction in this waste by designing and fitting a collar to the raw material bins to change the air flow, and by experimenting with the extraction settings to achieve the required air cleanliness while minimising raw material losses. The cost of making the collars was approximately $100.

Hand packing of ampules

300,000 packs of ampules were received in bulk form each year. These packs were then packed into boxes by hand. It occurred to the SCIP team that the blister line's high-speed packaging machine could be used to pack the ampules automatically. It was previously not thought possible by management to use this machine for ampules. After some discussion and experimentation by the team, they decided to fit a new detector. This was done using in-house designed and manufactured tooling . The cost was approximately $2000.

The changes made were successful. By automating this previously manual packaging task, 2000 hours of direct labour time was saved, which translated into $40-50000 dollars in cost (casual labour was used, so no full-time jobs were endangered by the change). Throughput was six days quicker.

Capsule counter

Two different machines were traditionally used to count tablets and capsules. The 'tablet' counter was much quicker than the 'capsule' counter. The 'capsule' counter was brought out whenever the capsules were to be packaged. This was relatively infrequent - 4 times per year, requiring 9 days on the packaging line per occasion at the rate of 130 packs per hour.

In factory parlance the two machines were known as "the tablet counter" and "the capsule counter" but they were essentially the same in function. With the introduction of SCIP, current practice was no longer taken for granted. A new franchise for change opened up the possibility that both machines may be thought of as "counters" and the most efficient one should be used as much as possible. (SCIP not only affected mindsets, but mobilised changes which had previously been mooted but were never followed up.)

For a cost of $8000, a new set of slatts was purchased for the newer machine to allow it to handle capsules. This increased packaging speed for capsules from 130 per hour to 2000 per hour. The saving in direct labour costs was $12000 per packaging run. This was a significant saving, but the principal benefit was that packaging run times were reduced from 9 days to one. This made the packaging line free for an additional 32 days of production per year. The quicker turnaround also meant that tablet orders no longer had a potential additional 9 day wait (when capsules were being produced), so tablet inventory could be reduced with affecting order fulfillment.

Tablet coating

There was a high level of variability in tablet coating times. For average 10 day runs, the time taken could be plus or minus 3 or 4 days. This meant scheduling other processes dependent on coating was very difficult. Tablet coating runs took place only 4 times a year but they were very disruptive to packaging schedules.

Efforts were made to trace the sources of variation but these proved elusive. Times could not be traced back to either ingredient variations or machine settings. The variation could not be reduced.

The only benefit resulting from the exercise was that they found that scheduling was more accurate if modal rather then average coating times were used in production time estimates.

RF terminals in the warehouse

RF (Radio Frequency) terminals for use by warehouse picking staff had been considered for some time. The warehouse staff decided to use SCIP tools to implement the project and formed a special team. It took two months to implement the new system. Going on previous experience, it would have taken 6 or 7 months without the use of the SCIP team approach.

This project was an example of process re-engineering. Prior to the RF terminal introduction, orders were entered into the computer system to produce a picking slip. This was placed in a vacuum tube and sent to the warehouse. The warehouse operator would then take the picking slip into the warehouse and pick the goods listed, ticking off each order line as it is picked, and noting any "out of stock" adjustments on the slip. The slip was then returned for invoice generation. The picking slip was easy to misread, and pharmaceutical goods are notoriously difficult to pick because products often only differ in terms of pack sizes and concentrations. Names of products also tend to be very similar.

Any adjustments slowed invoice printing, so in many cases goods had to be shipped without invoices, delaying payment times and incurring additional mailing, handling, and reconciliation costs.

With the RF terminals there is no delay between order entry and despatch of information to the warehouse. Warehouse operators are able to pick goods line by line from the terminal display and confirm that the correct goods have been picked using a bar code reader. Any "out of stock" adjustments are entered there-and-then by the operator, adjustments are made instantaneously by the computer and invoices printed immediately. As a result invoices are always sent with the goods.

Prior to the RF terminals, picking errors were 3-5% in the worst months. These errors were reduced to an average of 0.1% per month, and these were restricted to quantity errors only (incorrect goods errors were completely eradicated).

Packaging room

A proposal was put to management to re-arrange the packaging room and refurbish it by installing different feed mechanisms. The cost of this was estimated at $80,000 and the projected savings were estimated at $50,000 per year (half a person and increased throughput times).

Head office approval was required for all capital expenditure over $10,000. Approval could not be secured, not because the proposal was unsound, but because there was a blanket ban on capital expenditure.

Overall results

In overall terms the results of the program were spectacular. Easily measured cost savings on initiatives taken in the first six months totalled $70,000 per year on total outlays of only $10,000. Further savings of $50,000 per year were identified but required capital expenditure to realise them. In addition, very significant other benefits were secured in terms of difficult-to-measure savings, quality improvements, and reduced risk of accidents or damage. Consulting and training cost $24,000.

Benefits could be expected to increase significantly as the program matured. Most of the initiatives were reported as coming from the combination of new teamwork skills, observation, and being given a franchise to change things. The hard-edged analytical tools, including statistical process control, were yet to make an impact.

A sad end

SCIP achieved its success despite some internal resistance. The QA manager, although outwardly cooperative towards the manufacturing manager and the consultant had, it appeared later, always been anti the program. His view was that anything to do with quality was his preserve and that the idea of engaging staff to help improve processes was "a wank". Despite his antagonism, his staff, who had all been through the training, were enthusiastic. They were assigned to various teams and wanted to continue to work with them. The QA manager resisted at every turn; "I do not want to see anyone doing anything that there is not an SOP for", he was often heard to say.

The warehouse manager left the company a few months after program implementation. He was replaced by, "an accountant with a chip on her shoulder", as she was described by one staff member. She was interested only in cost-cutting and analysing the numbers. She had no time for teamwork, SCIP, or its aims, which ironically was her best strategy for achieving what she was looking to do.

But these negative forces did not bring about the end of SCIP. It had built up enough momentum to carry on through this resistance and would probably eventually have overcome it through its demonstrative success and enthusiastic champions. The end came when a multi-national strategist decided that, at 0.2% of international production capacity, Summer Pharmaceuticals could afford to do without its Australian plant so it was shut down at a de-commissioning cost of $11M.

The above story unfolded some years ago. If the company had acted on the basis that it had a high-quality, efficient, and productive pharmaceutical manufacturing capability in Australia and asked, “What is the best use we can make of this?”. rather than, “We need to reduce some costs – what can we easily chop out?”, then Summer might now have captured a high proportion of the Australian pharmaceuticals manufacturing market, to its own and Australian consumers’ benefit. We may well have been saved the economic and social cost incurred by the less scrupulous and cynical operators that subsequently moved in to fill the vacuum that was created.

First published 2003

This article may be reproduced only with the permission of HCi . Copyright HCi, 2001-3.

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