Another Job Interview, another unhappy with myself

Today I attended an interview for a science role. I prepared. I researched. I got questions I’d not expected.

Despite my preparation using examples based around the STAR method, my answers were week, being generalisations, or examples that were not fresh in my mind.

The position I was being interviewed for today was basically a team leader role for a bunch of process validation staff. Something I think is suited to my skills, would be sufficiently challenging and keep me busy. My preparation focused on my strengths, how I motivate and lead teams, how I’d developed teams through training. I also focused on my GMP and QMS knowledge, but nothing about that was asked. I’m thinking I should spend a day a week reviewing this sort of stuff so the next time I get an interview, I handle it like a pro. I think I put in a better performance than my last interview, but it was still lacking.

So, here are the questions I was asked, but had to wing…

Q: Give us an example of how you have influenced people and brought them around to your way of thinking…

A: I used some example about how my manager was a chemist and I am a microbiologist. Chemists deal in absolutes, microbiologists deal in probabilities. A weak example of test results, repeat testing and the eventual result being in line with my original expectations and how, over time, my manager was more likely to take on board my advice.

Thinking back, I could have adapted my “how do you motivate people” answer, but that would have still been poor as it is a general answer and not specific.

Q: Give us an example of working on a project team. What was your role and what input did you provide. Who were the other members?

A: I used a site consolidation example I winged. I did not give a strong answer as to what my role was (it was as a microbiology consultant). My contributions were stated more or less and I emphasized how I’d proactively provided microbiology floor plans. I could have been clearer about the other member’s role. I then threw in how I’d lead a regional group of microbiologists through method harmonisation.

Q: Give us an example of when you have mentored and developed staff…

A: I used some example related to an assay falling over. I should have used an example of observing an analyst, suggesting improvements to their technique and how I’d share my scientific knowledge with them. I would have still needed proof that any of that helped them improve.

Q: Give us an example of how you have made process improvements.
A: More weak examples with some specific examples about micro identification methods of assay methods being improved being dragged out of me.

I used “I” a hell of a lot more than “we” to show I did things (as that is what the last interviewers wanted). Applicants will be contacted next week with a yay or nay.

I think the only thing that impressed the two interviewers was how I’d developed a 12 month training plan for my team with a training session each month.

The ABC’s Catalyst and Dodgy Science

Catalyst, a science digest program on the ABC, for the last three weeks has been running stories on the evils of sugar. I suspect a recent push by some nutritionists is the root cause. Not having the program constantly run stories about climate change is a nice change though – there is far much more science going on in the world than studies into humans increasing the mean global temperature over time.

Here’s a summary:

  • 3 weeks ago – diet and tooth decay
  • 2 weeks ago – how sugar is the new evil
  • 1 week ago – how energy drinks are dangerous

Continue reading

Finally Dabbled with Moodle

For a while now I have had the idea to turn a power point presentation I developed a number of years ago into an online learning module. A couple of weeks ago, I set up a domain specifically for playing with Moodle and installed it. I then had to uninstall it as my host’s server’s version of SQL is a bit long in the tooth to support the current version. Once I found a compatible version I unzipped it on my server, set up a database with a couple of test users and had a click around the installation.

I had no troubles creating a course directory structure, but how one went about adding content boggled my mind (it was probably 3 am when I did all this).

This evening, I thought I’d have a fresh look at things and after about 3 hours of referring to my old power point presentation, I’d ported enough information from it to make a fairly decent, but basic and no frills training package on how to control microbes in the home.

Looking at things, if (and when) I have a go at developing some more training modules, most of the fancy formatting will probably be done in Dreamweaver and then copied across to Moodle as I’m not too keen one the provided text editor.

If you want to check it out, click here to learn a little about microbiology. (link’s dead as I’ve removed the site – Jan 2016)

Cover Letters & Resumes

In my quest for employment, I’ve been submitting boring old cover letters to the roles I apply for. The general advice for designers is to send in a fancy pants cover letter. That’s not something I’ve been doing until recently. This week I figured I would start doing that, both for design and science roles.

This last week, I sent off two job application with themed cover letters. One for a design role, one for a science role. I received a call back for the science role (no botching the interview answers this time I hope).

For some “fun” I’ve redacted some information on the doccos. The design role was written and designed as a press release. The science role was created as a controlled document.

Science role cover letter

 

Design role cover letter

Design role cover letter

In addition to creating themed resume’s I redesigned my scientific resume into a controlled document format which can be customized for the role being applied for. Check out the redacted version here.

Did you find this informative or useful? Please consider a small donation so I can expand and improve on what I deliver.

Anti Ageing Docco

This evening on SBS I watched a documentary about “the truth about” skin ageing. Half of the program appeared to be a plug for Unilever. They had conducted a study into a pill they say rejuvenates skin. This study included a few hundred women (so a fairly small sample size) and made some pretty weak claims based on the good old “before and after” photo. Nobody has independently reproduced or verified the study.

Another section of the docco detailed how “Loreal is the leader in producing artificial skin”. Even without looking up any info, I can tell you that is crap. There are a number of medical companies who are working on creating artificial skin, and most of them use discarded skin as a starter (so grow skin, even if the end product is termed artificial).

In the end, the docco did not deliver. Pleasingly, it did treat the viewer like they had an attention span and told four stories in order, with no jumping all over the place or summarising the entire program after the ad break.

I got the impression the presenter was relaying press releases from cosmetic companies, rather than providing real science. They did mention small sample sizes and whether or not the studies had been peer-reviewed.

Job Interviews Are Not My Forte

Today I attended an interview for a science role. I’m never happy with my interview performances, so I like to prepare. This takes the form of researching a little about the company and working out likely interview questions. Despite this, normally a question or two gets that asked is not one that I have prepared for, so there is a little winging it, but not too much. For those questions I expect, if it calls for it, I have my answers already written down in STAR format. In the absence of notes, I tend to deviate from the pre-packaged answers so they do not sound rehearsed.

Today, I get to the interview and rust starts falling off me. The standard questions ‘tell us about your(self) career so far’, ‘what are your strengths and weaknesses’, ‘how do you make difficult decisions’ etc were asked. I have prepackaged answers for all of these which are good. Did I provide competent answers? Umm, no.

Three questions I also did not prepare for were ‘tell us about a time you dealt with a (customer) complaint’, ‘what sort of manager do you prefer’ and ‘what do you expect to be the greatest challenges in this role’. For that last one, that is a question I like to ask the interviewers, so being asked it myself through me for a loop. I also used “we” a lot in my answers, indicating I was giving a hypothetical answer, rather than “I”. That stems from my collaborative work style.

So, instead of my el crappo in a hatto answers, here’s how I should have answered.

Q: Why do you want to work in QA when you have a microbiology/QC background?
A:
I see the role of QA as being proactive while QC is reactive. In life I like to plan and be proactive in what I do so a QA role is more suited to my personality than the reactive QC role. Besides that, I see a QA role as a good opportunity to use my auditing skills, increase my knowledge of pharmaceutical processes and enact positive change (whether it be improved documentation, processes or other).

Q: Tell us about your strengths…(here I came up with one or two of them, but did not answer very well IMO)
A(a): I am quick learning
The most recent evidence of this is the DaVinci Award I received as part of my Diploma of Commercial Arts. It is given to the individual who improved the most over the duration of the studies. It shows I can take on new knowledge and apply it effectively.

A(b) I am flexible
In my previous role, my work day was not set in stone. When an unexpected sample arrived or I needed to attend to something unplanned for the day, I was able to rearrange things and not feel put out. As a scientist, I am flexible in my beliefs. I may believe faster than light travel is impossible now, but prove to me otherwise and I’ll update my beliefs. When I was studying part time, I needed to balance my study commitments with my full time work and my leisure time. Show me why your way is better than mine and I’ll adopt your practices, or modify them to improve my own. (Bit of a hodgepodge of answers, but it gets the point across).

A(c) I am good at planning and organising
Having been involved in many projects over the years and not having access to a program such as Microsoft Project, I took it upon myself to create my own gannt chart. This enables me to track what I am working on and assign dates for completion. This has come in handy in the case of test process validation as one can see that certain steps need to be completed before others. By using a chart, it is also easy to see where a step takes longer than planned or predicted and one determine if such as step can be hastened. Eg for some non priority reports, it may take months to get final signoff. The use of SMART goals also helps with planning. If there is no clear output from a task, then there is no real point in the task. As a cyclist, I have an annual training plan I develop each year which incorporates SMART goals.

A(d) I am great at checking documentation
When I am checking other’s paperwork, I pick up errors and omissions like a hawk and feed this back to the originator for correction.

Q: Tell us about your weaknesses…(only came up with one of them).
A(a): If it is my own paperwork, it needs to be put aside for about a day before I proof read it
Thanks to having good visualisation skills, when writing documents, my mind can race ahead of my fingers. This can lead to some strange wording. If I proof read a recently written section of text I’ll also see what I remember writing, not what is actually there. I find putting the work aside for about a day and proof reading it then leads to a quality document.

A(b): If I have imagined it happened, then I think it has.
Due to my visualisation skills, often if I think of doing a task, I’ll swear I actually did it. To address this, I like to keep a to do list and check it off when tasks are complete. That way I can document that I have done something, rather than remembering (incorrectly or not) that I did it.

The customer complaint question was tricky as I’ve not dealt with these directly. The only exposure I have had is with testing samples from complaints and reporting back on the results as well as proof reading customer complaint reports and suggesting additional investigations or text clarifications. In reality, if there was a complaint, then it would be dealt with according to established procedures (which if they did not exist, I would research what to do and then document it)…

Q: How Have You Dealt With Customer Complaints?
A: I have not dealt with these directly, however I have examined and tested samples from complaints and reported back on the results as well as made recommendations as well as proof read customer complaint reports and suggested additional investigations or text clarifications. In reality, if there was a complaint, then it would be dealt with according to established procedures (which if they did not exist, I would research what to do and then document it).

Examples of my role in the customer complaint investigation process include: a) I tested black spots on a disintegrated tablet that had been returned from Brazil. The spots were found to be Penicillin which I determined probably came from the user’s environment. I provided a report of my investigations to the customer complaint officer in QA.  b) More recently, I was consulted with regularly  by a member of the lab who had been seconded to deal with customer complaints. I would regularly proof read their reports and suggest improvements in grammar or information flow.

Q: When have you made a difficult decision (this one started out ok, but degenerated).
A: I never make difficult decisions as once all factors have been examined, the only possible decision of the logical one
Once I gather all available data, it is weighed against the regulatory requirements, internal requirements, risk assessment tables and any other relevant spec and then a decision is made.

An example would be when I was on an interview panel for a new microbiologist for my team. Two of the candidates appeared equally suited for the role. Whoever scored more highly on our list of essentials got offered the role.

The actual answer I gave dealt with needing to retest a buggy sample and deciding on what to do, which was not difficult (as demonstrated by the “good” answer).

As well as these, there was the standard ‘where do you see yourself in the future, job wise’ question which I tend never to answer well as long as I am learning and applying my knowledge and skills, I am have no preference for what I am doing or how much responsibility there is.

Q: What sort of manager do you prefer
A:
One that appears to be trustworthy, has a clear direction for their team and ensures the team has the skills, training and resources in order to get the job done. They support their team’s decisions and provide direction (but not solutions) to issues that arise. The best leaders are those that on the face of it, do nothing while in reality, they are behind the curtains, pulling the strings and keeping their team on target.

So, that’s how I should have answered. Worse case is I do not get a second interview. At least I get to add/modify my list of interview questions and answers.

Notes on International Standard ISO 13408-1: 1998(E)

One of the main International Standards used as a reference document in a sterile pharmaceutical microbiology laboratory is ISO13408 – Aseptic Processing of Health Care Products .  Long ago, I reviewed the 1998 edition.  The 2008 edition of the standard was last reviewed and confirmed in 2011 as current.  Part 1 details the general requirements.  The 2008 edition is edition 2 and is a techncial revision of the 1998 document.  The guts of the standard are not dissimilar to version 1.

My review of the 1998 edition follows.  When I get my hands on the 2008 edition, I’ll review that with reference to this review.

The use of italics is my way of emphasising points. Continue reading

Notes on USP31-NF26 <1116 - Microbiological Evaluation of Cleanrooms and Other Controlled Environments>

Modified 20181212 – minor typos corrected. minor updates.

The USP is the United State’s Pharmacopeia.  If you are selling pharmaceuticals in the USA, you need to follow the USP and are subject to FDA regulation.  For the layperson, a pharmacopeia is an official publication containing a list of medicinal drugs with their effects and directions for their manufacturing, testing and use.

I last reviewed USP 1116 in 2009 when it was version USP31–NF26.

Where one does not have direct access to the USP (it is behind a pay wall),  there are plenty of sites that review changes and publish their considered opinions.  The USP itself publishes Revision Bulletins, IRA’s (public comment documents showing proposed changes) and Errata.  From these one can build up a fairly accurate picture of the USP.

The latest iteration is USP 41–NF 36 — this became official on May 1, 2018.  The last version I managed to get my hands on was USP36 NF31.  What follows is my original review. Continue reading