As a Regulatory Affairs Officer you are the crucial link between the R&D department and Quality Management department. Your responsibility is to coordinate the registration of (new) products in accordance with scientific, legal and pharmaceutical regulations. You will write product licensing proposals, undertake regulatory inspections and interpret research or trial data. For this position, you will participate in different projects and will communicate with regulatory authorities and institutes on a regular basis.
This job is situated in the northern regions of the Netherlands, our client is a well-established company in the pharmaceutical industry. On site, the company develops and manufactures health care products which are marketed worldwide. It is known for its integrated knowledge centre where research and development result in specialized and innovative pharmaceutical products that enable high-quality health care.
* Bachelor’s or Master’s degree in Pharmacy or a congruent discipline
* At least 2 years work experience in Quality Management or Regulatory Affairs *
* Proficient in written and spoken English
* Additional qualities: accurate, result-driven, able to think strategically, has excellent organizational and communication skills.
Please apply with your CV and cover letter by the 'apply' button below
Education Backgrounds: |
Biomedical Science Healthcare Science |
Specialties: |
Biomechanics / Tissue Biomedical Engineering Biomedical Imaging / Modelling Life sciences Pharmaceutics |
Education Level: |
Undergraduate (Bachelors) Postgraduate (Masters) Doctorate (PH.D) |
Experience: |
2 - 5 years 5 - 10 Years |
Languages spoken: |
Dutch English |
Job Location: | , Netherlands |
Type: Job
Deadline: 25th July 2013
Job reference (ID): 6163
Loading...