FUJIFILM Biotechnologies
Qualification Engineer
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
Job Title: Qualification Engineer
Location: Billingham, UK
About the role
We’re seeking a Qualification Engineer to ensure GMP manufacturing, QC, and supply chain systems are validated, controlled, and inspection-ready. You’ll plan and execute qualification activities across equipment and utilities, project-manage asset support work, and embed best-practice operating methods that improve reliability, compliance, and performance.
What you’ll do
- Plan, schedule, and maintain the qualified status of GMP equipment and utilities across manufacturing assets.
- Deliver inspection readiness through robust qualification, documentation, and lifecycle management.
- Execute improvements to equipment and utility systems using risk- and data-driven insights.
- Lead or support investigations for deviations, QIPs, and CAPAs; author test plans, protocols, and reports.
- Act or deputise as VSP Owner for direct-impact equipment and utilities.
- Provide system expertise to promote best-practice operating methods across Manufacturing, QC, and Supply Chain.
- Interface with internal/external SMEs to stay current with regulations and technologies impacting GMP assets.
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
What you’ll bring
- Honours degree (or higher) in Engineering, Microbiology, or a related technical field.
- Strong understanding of GMP and validated state for equipment/utilities.
- 3+ years in Commissioning & Qualification (C&Q), Validation, or Compliance, with a track record delivering protocols, test execution, and reports.
- Hands-on experience with:
- Moist Heat Sterilisation, thermal mapping, biological indicators, steam quality testing.
- HVAC, LAF, MSC testing; VHP systems (e.g., Bioquell Qube isolators).
- Controlled temperature chamber mapping.
- Tools and systems: Microsoft Office, SAP, Siemens SCADA/PCS, TrackWise, Kneat, Veeva.
Get help with your application
Your very own career expert that helps elevate your application to the next level.
Why join us
- Make a tangible impact on product quality, compliance, and operational reliability.
- Collaborate with cross-functional experts and grow your CQV/validation expertise.
- Training and development opportunities aligned to regulated manufacturing environments.
- Competitive salary, with 35 days holiday (Not including Public Holidays), competitive pension: you contribute 4–9%+ and we contribute 7–12% (up to 21% total), with flexible investment/retirement options.
We are committed to providing equal opportunities in hiring, promotion, compensation, benefits, and training—regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national or social origin, disability, or veteran status.
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills