Regulatory affairs Specialist At EVA Pharma
Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.
Job Summary
We are seeking a detail-oriented and driven Regulatory Affairs Specialist to join our dynamic team.
The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry.
Key Responsibilities:
– Prepare and submit regulatory applications and documentation to the appropriate authorities within Europe.
– Review and assess product labeling, promotional materials, and technical documentation for compliance with regulatory requirements.
– Maintain knowledge of current and evolving regulations in the pharmaceutical sector, particularly within the European Union.
– Act as the liaison between the company and regulatory authorities, facilitating communication and addressing inquiries or issues.
– Support the development of regulatory strategies for new product registrations and life cycle management.
Requirements:
– Bachelor’s degree in Pharmacy, Life Sciences, or a related field.
– 1-3 years of experience in regulatory affairs within the pharmaceutical or healthcare industry.
– Knowledge of EU regulatory frameworks, guidelines, and procedures.
– Excellent communication skills, both written and verbal, in English; proficiency in additional European languages is a plus.
– Highly organized with the ability to manage multiple projects and deadlines effectively.