Experis Life Sciences is your partner in your research for professional opportunities.
Our expertise and our large client portfolio in the pharmaceutical, chemical and food industries allows us to make the good connections between your experience, your expectations and the needs of the market.
You will have the opportunity to enter various departments (R&D, Production, Supply Chain, QA, QC, RA, ...) according to your interests.
Interested by Documentation and Quality compliance? This position is for you.
Your responsibilities :
The worker will be part of Process Development Group and based at the Lessines Pilot R&D. He/She will organize periodic review of SOP & forms, the writing of qualification protocols and reports of Pilot equipment, manage creation and follow-up of failure events, perform/manage all necessary tests linked to these documents
In collaboration with customer, internal experts, IT, EHS, Engineering and Quality Assurance departments:
Our offer :
Do you recognize yourself in this mission and want to know more?
Contact me : or 0476/86.79.24
If you do not find yourself in this offer but are looking for opportunities in the pharmaceutical industry, feel free to send your CV and visit our website www.experis.be
Other opportunities are available and may be suitable for you.