As part of a site wide modernization program, the resource will report and provide support to the local program lead. He/She will be responsible for the validation & qualification activities of shopfloor systems including data integrity. The scope includes automation systems, computer systems and equipment's linked to pharmaceutical manufacturing. All of this in accordance with our company standard processes and compliance rules.
Qualification & Validation
o Creation of validation lifecycle documents (Requirements, Design specs, FAT/SAT, IQ/OQ/PQ) according to the MSD standards
o Testing of shopfloor systems
o Execution of validation protocols
o Creation of Standard Operating Procedures
o Support operations/production at startup of project
– System Validation Lifecycle
– Pharmaceutical Industry and Standards (GDP, GxP)
– Dutch/English (Verbal/Written)
– Minimal experience and knowledge of GMP, GDP and qualification in a pharmaceutical engineering environment
Wat bieden wij?
Tormans invests in your future by offering appropriate training, personal guidance during the execution of your projects, advice and customized coaching.
Our projects are located at the most important (inter)national companies in various sectors, which means you will be introduced to the most modern techniques and the most diverse installations so that you can develop your knowledge and talent to the fullest
In addition to an open-ended contract with an attractive, tailor-made salary, we offer numerous extra-legal benefits, including meal vouchers, a daily allowance, company car with fuel card, hospitalisation insurance,..
At Tormans you can count on a professional, personal and honest no-nonsense approach.