Regulatory Affairs Expert
2 days ago
Job Title: Regulatory Affairs Expert - Pharmaceutical Product Registration
Overview:
Lifelancer, a talent-hiring platform in Life Sciences, Pharma and IT, seeks an experienced Regulatory Affairs Expert to join our team. As a key member of our regulatory department, you will play a crucial role in ensuring the timely registration of pharmaceutical products with regulatory authorities.
About the Role:
We are seeking a highly motivated and organized individual with a strong background in regulatory affairs. Your primary responsibility will be to develop and implement effective regulatory strategies for new product registrations, ensuring compliance with local and global regulations.
Responsibilities:
- Develop and implement regulatory plans for new product registrations, including timelines and submission requirements.
- Collaborate with cross-functional teams, including product development, manufacturing, and quality assurance, to ensure regulatory compliance.
- Prepare and submit regulatory documents, including dossiers and labels, to relevant authorities.
- Maintain accurate records of regulatory submissions, approvals, and post-approval activities.
- Stay up-to-date with changing regulatory requirements and provide recommendations for process improvements.
Requirements:
- Bachelor's or Master's degree in a related field, such as pharmacy, chemistry, or biotechnology.
- Minimum 3 years of experience in regulatory affairs, preferably in the pharmaceutical industry.
- Strong knowledge of local and global regulatory requirements for pharmaceutical product registration.
- Excellent communication and project management skills.
- Ability to work independently and collaboratively as part of a team.
What We Offer:
- An estimated salary of $85,000 per year, commensurate with experience.
- A dynamic and supportive work environment.
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