Regulatory Affairs
hace 4 meses
**Purpose of the rol**:
Asphalion is growing and we are looking for a Regulatory Affairs Officer to join our procedures team in **Portugal** with experience within pharmaceutical industry Someone who loves to take new challenges, to work in an international environment and who wants to grow with us
**Main responsibilities**:
Submissions of NA, variations, renewals and procedures national and worldwide, including EU, US, CH, Rest of the World (RoW), etc.
Pricing and Reimbursement
Request to Health Authorities
Due Diligence
Data-entry of clinical trials
Adapt the documentation to the Transparency Policy 0070
Strategic Regulatory Advice
Review of promotional material, packaging & labelling
According the project all activities can be done for medicinal products, medical devices, cosmetics, biocides, and other regulated products.
**Requirements**:
- +2 years experience experience in Regulatory Affairs Pharma departments.
- Fluent in English
- **Based in Portugal**:
- Academic Degree in Life Science.
- Advanced IT level - (MS Office). Proactive, good communication, accurate, detail orientated.
**We offer you**:
A highly, dynamic & international working environment with employees from more than 15 nationalities.
A professional, inclusive and high-performance work environment to develop your skills and grow your career.
A great company culture built around Passion, Flexibility, Commitment, Quality & Companionship.
Training and personal development program.
Flexible working schedule - Compacted workday on Friday.
Social Benefits: English lessons, wellbeing programme, flexible remuneration.
Permanent contract.
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