At a Glance
- Tasks: Own the process validation lifecycle from concept to release, improving and rebuilding systems.
- Company: Growing Medical Device manufacturer focused on quality and innovation.
- Benefits: Competitive salary, hands-on experience, and opportunities for professional growth.
- Other info: Onsite role with a focus on continuous improvement and quality engineering.
- Why this job: Make a real impact by enhancing validation processes in a dynamic environment.
- Qualifications: Experience in equipment or process validation within Medical Device or pharmaceutical manufacturing.
The predicted salary is between 37800 - 46200 £ per year.
I am looking to speak with Quality Engineers who genuinely understand process validation.
Not just reviewing protocols someone else has written, but actually owning it.
From concept and design, through IQ/OQ/PQ, to final release.
I’m working with a growing Medical Device manufacturer looking for someone to take real ownership of their process validation lifecycle and there’s plenty to get stuck into.
The validation process needs a few tweaks to ensure that the risk based approach flows through properly into what actually happens on the ground, and they want someone who can come in, work out what needs improving and rebuild it properly.
Initially, around 70% of your role will be focused on validation.
You’ll be looking at
- The full process validation lifecycle
- IQ, OQ and PQ
- Risk and impact assessments
- SPC and process capability
- Measurement System Analysis
- Improving templates and documentation
- Making validation genuinely risk based, rather than a tick box exercise
The other side of the role is broader Quality Engineering.
Using data to understand how processes are actually performing and spotting problems before they become NCRs or CAPAs.
Over time, the role moves more towards oversight.
You’ll be the person setting the standard for validation and guiding teams as new equipment and processes are introduced.
They’re not looking for someone who has supported validation from the sidelines.
You need to have owned equipment or process validation yourself, ideally within Medical Device or pharmaceutical manufacturing, and be confident taking something from concept all the way through to release.
If you’ve done that and want a role where you can actually improve how validation is done, rather than inherit a perfect system and maintain it, this could be a really good one.
Please note, this role is quality within a manufacturing environment focused on improvements to processes, so naturally it is ONSITE.
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Quality Validation Engineer in Cambridge employer: Medibeam
Join a dynamic Medical Device manufacturer that values innovation and ownership in the Quality Validation Engineer role. With a strong focus on employee growth, you will have the opportunity to lead process validation improvements and set new standards in a collaborative work culture. Located onsite, this position offers a unique chance to make a tangible impact in a thriving industry while working alongside passionate professionals dedicated to quality and excellence.
