beeldscherm schreef op 8 november 2017 09:39:
Pharming Group N.V. Regulatory Affairs Biomedical (Senior) Specialist - Leiden
Active since 06-11-2017 Job category Quality / Health / Environment ...
Location Leiden Level Professional
Educational level Master / Post-Graduate / ... Employment type Fixed term contract with option...
Hours 32 - 40 Salary
Introduction
Pharming Group N.V. develops innovative protein therapeutics for the treatment of genetic disorders. As the Company further develops, its legal complexity will be increasing thus requiring strengthening of its legal functions.
At this moment, the company is composed for further science, technology and new product development and commercial roll-out. The company is small (approx. 130 employees, based international) and entrepreneurial. The Regulatory Affairs Biomedical (Senior) Specialistmust fit in this organizational culture where integrity, entrepreneurship and flexibility are core competencies.
Job description
Currently we are looking for a Regulatory Affairs Biomedical (Senior) Specialist. In this role, you will be responsible for your own projects. Depending on your expertise and interests, you will be involved in the interaction with the Pharmacovigilance Department, Marketing & Sales, Market Access activities, Medical/Clinical, Regulatory labelling, or eCTD publishing activities. Depending on expertise and experience, you’ll be involved in all regulatory (non-CMC) activities.
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