A career is an ongoing journey of discovery: our 52,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. For 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.
Your Role: An exciting opportunity has arisen to join our team as a Validation Engineer. Within this role you will support the site to ensure all processes and procedures are fully compliant with ISO9001; ISO13485; 21 CFR 600; IVDD 98/79/EC and other appropriate regulations and standards. You will write and complete protocols and reports, provide guidance and support to all departments/staff as needed, maintain on-going understanding and knowledge of the latest regulatory requirements for validation and support the maintenance and execution of Validation Master Plans for Site Specific Production departments and Corporate Initiatives.
Who You Are:
- Degree educated in quality or science related discipline
- Previous Validation experience within a cGMP environment is essential
- Strong analytical and problem-solving skills
- Excellent communication skills with the ability to collaborate and present at all levels
- Competent in the use of IT (Word, Excel, PowerPoint)
What we offer: With us, there are always opportunities to break new ground. We empower you to fulfill your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!
Curious? Apply and find more information at