A specialized recruitment firm is seeking a Senior Regulatory Affairs Specialist in the Netherlands. The role requires responsibilities in obtaining licenses and creating packaging materials to ensure compliance. Ideal candidates will have a degree in relevant fields, at least 2 years of experience in the pharmaceutical industry, and proficiency in English. This is a full-time position focusing on Quality Assurance within Pharmaceutical Manufacturing.
Qualifications
Minimum 2 years of experience in the pharmaceutical industry.
Experience in QA or RA within pharma is a plus.
Fluent in English and good knowledge of local language.
Responsibilities
Prepare and submit dossiers for parallel trading licenses.
Create and maintain packaging materials and artwork files.
Manage and archive regulatory documentation.
Skills
Attention to detail
Proactive collaboration
Professional proficiency in English
Education
Master’s or Bachelor’s degree in Pharmacy
Degree in Regulatory Affairs or Life Sciences
Tools
Adobe InDesign
Illustrator
Photoshop
Job description
A specialized recruitment firm is seeking a Senior Regulatory Affairs Specialist in the Netherlands. The role requires responsibilities in obtaining licenses and creating packaging materials to ensure compliance. Ideal candidates will have a degree in relevant fields, at least 2 years of experience in the pharmaceutical industry, and proficiency in English. This is a full-time position focusing on Quality Assurance within Pharmaceutical Manufacturing.