In this role, you will play a key part in ensuring robust process, cleaning, and packaging validation across the full lifecycle, from planning to shop‑floor execution
Job Summary
In this role, you will play a key part in ensuring robust process, cleaning, and packaging validation across the full lifecycle, from planning to shop‑floor execution.
Working closely with cross‑functional teams, you will help maintain GMP compliance, drive ongoing process verification, and ensure inspection readiness through strong technical expertise and high‑quality documentation.
Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world.
Matching Summary
In this role, you will play a key part in ensuring robust process, cleaning, and packaging validation across the full lifecycle, from planning to shop‑floor execution.
Skills & Requirements
Must-have
Process validation
Cleaning validation
Packaging validation
GMP compliance
Ongoing Process Verification
Nice-to-have
Quality risk management
Cross-functional collaboration
Inspection readiness
Reimagining medicine
Key Requirements
Bachelor’s degree in Chemistry, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or related field
2–3 years of experience in pharmaceutical manufacturing, MS&T, technical development, or quality
Experience with process validation and writing/reviewing technical reports
Fluent in English and proficient in the local site language