In the position of Corporate Quality Compliance assistant, you will be mainly responsible for the handling of a variety of Good Manufacturing Practice (GMP) documents. You will check whether the documents have been created according to Synthon procedures. You will arrange that the agreed documents will be supplied to Synthon’s customers. You will also handle additional requests from customers regarding documentation. Furthermore, you will assist Corporate Quality Compliance managers with administrative tasks. You will be part of a diverse team of 10 members and report to the department head. Your profile
Your letter of motivation and CV show that you have:
preferably an mbo degree in a relevant discipline
experience in a GMP environment and/or in the pharmaceutical industry is a plus
a good command of the English language
preferably experience with communication to customers
excellent verbal and written communication skills.
In interviews you will be able to demonstrate that you are quality and customer oriented, accurate and able to work well structured. You have an analytical mind and you have excellent planning and organizational skills. Moreover you are able to work under tight timelines. Last but not least, you are a team player. Application
Contract hours: between 40 and 32 hours.
Salary (fulltime): depending on experience, salary range € 2,700 to € 4,200 gross per month.
Location: Nijmegen.
For further information, please contact Paolo Conti, head Quality Compliance at tel. +31 (0)24 - 372 77 00. If you are interested in this challenging position, we look forward to your application. You can apply via the button/link.
Important dates
Please send your application before 1 December 2023. The first round of interviews will take place on 12 December 2023 and the second round of interviews will be on 19 December 2023.
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