Why Join SPGL?
A GREAT PLACE TO WORK
As a leading professional technical consulting group, we offer a friendly and dynamic environment to build your career and make an impact on the everchanging world.
Our highly respected group is powered by a diverse, innovative team who live by our ethos of quality, excellence & exceptional service. We handle multiple projects world-wide, largely through alliance agreements, for a variety of blue-chip companies including GSK, Pfizer, Estee Lauder and many others.
DIVERSE & INCLUSIVE
We think differently, taking a flexible approach when finding the brightest and most talented people to work with us. Our strength comes from our remarkable breadth of people and experience, but above all, our deep passion for quality, excellence & service
If you’re looking for a forward-thinking workplace and see yourself as a dynamic professional, who wants to be taken seriously and make an impact in today’s fast-moving world, come and be part of our success story.
YOU’LL LOVE WORKING HERE
Our people are the heart and soul of our organisation. Join our team and you can expect:
- A variety of challenging projects, with blue-chip customers such GSK, J&J, Pfizer
- A great mix of young and experience professionals
- International project assignments
- Modern offices
- Multi-cultural and caring organisation
- An equal opportunity employer
Do you have what it takes?
At SPGL we aim to attract highly motivated people, whatever their background, with a positive ‘can do’ attitude and a deep passion for excellence.
We are interested to hear from both graduates and experienced professionals. Typically, you will need to be educated to a degree level or equivalent in either mechanical/process engineering or a science discipline with at least 2 years relevant experience in the following sectors: Bio-Pharmaceuticals, Regulated Consumer Products, Chemicals or Mission Critical.
The successful candidates will be responsible for compliance with EU and/or USA cGMP requirements, preparation of engineering specifications, equipment inspections, commissioning & qualification plans, validation documentation (DQ, FAT, SAT, IQ, OQ and PQ protocols) and ultimately successful handover to the end user.