Company:
Our client is a leading biopharmaceutical company engaged in the discovery and development of innovative medical solutions. This company produces medicines and vaccines, including for chronic and rare diseases.
Role:
Contribute to the organizational documents by ensuring that registrations are obtained and compliance with regulations.
Responsibilities:
- Obtaining & maintaining registrations
- Responsible for optimal process control
- Contribute to PPM and PI strategy
- Responsible for the availability of the most up to date packaging and leaflet in the trade
- Problem identification and priority setting, providing relevant information for headquarters and branch office
Requirements:
- 4+ Years’ experience in Regulatory Affairs
- University degree in Medical, Pharmaceutical or Biomedical sciences
- Fluent Dutch & English
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About us
Since 2012, SIRE Life Sciences is the most innovative and engaged consultancy company for the life sciences industries.
SIRE Life Sciences is proud of its ability to adapt to changing trends while always maintaining the highest level of quality for both our clients and our candidates.
Our team of knowledgeable professionals provides customized staffing services to clients and candidates, including secondment, direct hire, temporary-to-hire, temporary staffing, brokering, Statement of Work and we approach each type with the same degree of professional assessment. Our refined and collaborative style is unmatched in the staffing industry. We’re able to see beyond the surface to create matches that result in successful careers for our candidates and valuable talent for our clients.
Effective employment solutions need to put the right person in the relevant place every time, using advanced systems to streamline costs and time-frames for clients.