QA & RA Associate Job in Groningen, Groningen Netherlands
Interesting position at young, fast growing pharmaceutical company!
Groningen
Offer
· A challenging and diversified job;
· the opportunity to deploy all your quality management talents;
· active contribution to the further development of the QA RA department;
· inspiring team and work climate.
Organization
Our client, New Neopharm (NNP) is a fast growing pharmaceutical manufacturing company. The core business of the company is (re-)packing and export of products for human and veterinary use. The product range is broad and consists of pharmaceuticals, medical devices, diagnostics and nutritional supplements.
The office of New Neopharm is located in Denmark, the Operations department is based in a small industrial area at the east side of the city of Groningen. A highly motivated team of 14 till 20 persons works closely together to deliver the products according to the high standards and within timelines. Due to a replacement there is a vacancy for a QA RA Associate.
Position
Together with the Qualified Person you are responsible for all quality and regulatory aspects of the materials, production process and the products, including writing and reviewing procedures for the quality manual. You will perform internal audits in the production area to ensure compliance to the SOPs. You are also responsible for the control and registration of temperature recordings and other process related and recorded parameters.
Another interesting part of the job is the handling of deviations and other quality-related issues. You will define corrective actions and ensure that they are implemented. Finally, you will contribute to all quality issues of incoming and outgoing materials including labels: receive certificates, apply for product licenses and maintain registration files. In short: a broad and challenging quality position!
Profile
· life science education, for example (assistant) pharmacist or farmakunde;
· at least 2 years experience in a pharmaceutical QA position;
· preferably knowledge of regulatory affairs;
· good knowledge of GMP regulations;
· handson; self-starting; accurate; quality minded and business sense; flexible;
· good knowledge of the Office software;
· dutch native speaker, fluent in English (verbal and written);
· available for 4 to 5 days, at least 25 hours pro week. Flexible hours (e.g. 9 – 15h) is possible.
Response
Interested? Please send your resume and motivational letter by Email, with reference to WS/11-061-MB to Mrs Annelien van der Hoek of Derks Derks: info@derksenderks.nl .
For further information, please call Mrs. Van de Hoek at +31 (0)33 472 80 87.
An individual assessment may be part of the selection procedure.
Our client has chosen Derks Derks B.V. as recruitment agency for this assignment. We request therefore to send any application or other response to Derks Derks.
http://www.derksenderks.nl/nl/nieuwe-baan/vacatures/QA_RA_Associate