Raboid Ruhsatlandırma Bilişim Hizmetleri ve Danışmanlık Ltd. Şti.

Ad/Name: Cansu

Soyad/Family Name: Dal Kaynak

Eposta/E-mail: cansu@raboid.com

Firma Adı/Company Name: Raboid Ruhsatlandırma Bilişim Hizmetleri ve Danışmanlık Ltd. Şti.

Pozisyon Adı/Position Name: Digital Regulatory Affairs Specialist

Pozisyon Tipi/Position Type: Sürekli/Tam Zamanlı

Alınacak Kişi Sayısı/Number of Employee to be Recruited: 1

İş Alanları/Fields: Ruhsatlandırma / Licensing

Adayın Çalışacağı Şehir / City: İstanbul(Asya)
İstanbul(Avr.)
Diğer

İş Tanımı ve Genel Nitelikler /Job Description and General Qualifications: Digital Regulatory Affairs Specialist

Location: Remote, Turkiye

About Raboid
We are an international RegTech company dedicated to driving innovation in global regulatory affairs for pharmaceutical companies through artificial intelligence-powered automations. Our solutions monitor official communications, conduct compliance analysis, provide data-driven insights, and generate customized regulatory affairs files for international submissions. We operate under the belief that in the rapidly advancing medical world, eliminating international boundaries & increasing compliance is essential to ensure quick and secure access to medicine for everyone. So, we're looking for someone who shares same passion with us.

Position Overview:
The Digital Regulatory Affairs Specialist will play a crucial role in enhancing our current AI powered RA automations, ensuring continuously AI integration for regulatory submissions, and maintaining RA compliance in the pharmaceutical industry. This position is open to candidates who are in Turkiye and are fluent in Turkish.

Key Responsibilities:
 Being responsible in development and maintenance of AI-powered RA automations.
 Utilize digital solutions for regulatory submissions, ensuring compliance with relevant regulations.
 Review documents of regulatory files generated by AI.
 Ensure that AI generated RA datasets are accurately produced and provide feedback to the development team for AI RPA enhancements or exception handling as necessary.
 Maintain and update databases, ensuring files are stored securely and reliably.
 Project management in RA projects for clients, adhering to set deadlines.
 Recommend process improvements to optimize semi-automated workflows.
 Collaborate effectively with both internal and external stakeholders.
 Stay updated on the latest regulatory changes and updates.

Qualifications:
 A bachelor’s degree in pharmacy, chemistry, chemical engineering, or a related field; an advanced degree is preferred.
 More than 2 years of experience in regulatory affairs.
 Excellent command of written and spoken English; proficiency in other foreign languages is a plus.
 Proficient in MS Office applications.
 Exceptional problem-solving skills with the capacity to adapt in a dynamic digital setting.
 Effective communication and collaboration capabilities.
 Detail-oriented with the ability to manage regulatory information and submissions accurately.
 A positive attitude and a flexible approach to teamwork.
 An organized and analytical mindset, focused on achieving results, ideally suited for a fast-paced and challenging entrepreneurial setting.
 Ability to plan multiple priorities concurrently and deliver high quality outcomes.
 A growth mindset, eager to acquire new skills, especially related to AI and RPA in regulatory affairs.

Why Join Us?
 Opportunity to be part of an innovation in pharmaceutical sector.
 Competitive salary and benefits package.
 Continuous learning and growth opportunities.
 A collaborative and inclusive work environment at an international organization.

Deadline for applications: 10th of May 2024

Raboid is an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees.