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: The QA Technician is responsible for the review of liquid and powder finished product manufacturing records and performing the disposition process. This work is carried out as outlined in the Integrated Management System and is performed to meet or exceed the product and service quality expectations of pharmaceutical, industrial and research customers as well as complying with the relevant standards of international regulatory authorities. The Regulations indicated here are those relevant to the manufacture of products utilised in drug manufacture, medical device applications and research as issued by ISO, EMEA and FDA guidelines.
Who You Are:
- Degree or equivalent in Biological Science or related discipline
- Previous experience working within a GMP environment would be advantageous
- Must be able to demonstrate attention to detail and apply a risk-based approach to operation
- Knowledge/experience of SAP and/or Track wise would be advantageous
- Ability to prioritise own workload
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!
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