GMP Validation Consultant / GMP Engineer (Freelance)
About this role
GMP Validation Consultant / GMP Engineer (Freelance)
An exciting opportunity is available for an experienced GMP Validation Consultant (or GMP Engineer) to support a specialist pharmaceutical manufacturing project in Japan.
This is a hands-on validation role supporting CMC and regulatory documentation activities, with responsibility for preparing, reviewing and organising critical validation documentation within a GMP-regulated environment.
This assignment is initially expected to run for approximately six weeks, with the potential for extension based on project requirements.
The Opportunity
Working alongside a highly experienced technical team, you will play a key role in supporting regulatory readiness through validation documentation, technical report writing and compliance activities.
Read the full description on TalentApply
Create a free account to see the complete job description, how well your CV matches this role, and apply in one click.
AI rewrites and formats your CV so it reads well and gets past screeners.
Get your match percentage for this exact role before you spend time applying.
Send a polished application in one click — no retyping the same details.
Follow every application in one place instead of digging through your inbox.
Free account · No card required
Your next opportunity starts here
Prepare, apply, track, interview and get hired — all from one platform, with AI in your corner.