Regulatory Affairs Manager: Thrive in a Dynamic Environment

hace 3 semanas


Madrid, Madrid, España Trium Clinical Consulting Nv A tiempo completo
Company Overview

QbD Group is a knowledge-based company specializing in development, clinical, regulatory, and compliance services for the life sciences industry. Our team is dedicated to providing tailored solutions that meet the unique needs of our clients.

Salary and Benefits

We offer an attractive and competitive salary package tailored to individual needs, taking into account local laws and regulations. In addition to a generous salary, we provide a range of benefits to support your personal and professional growth.

Job Description

As a Senior Regulatory Affairs Officer, you will play a key role in ensuring compliance with pharmaceutical legislation and regulations, including GMP. Your expertise in ICH guidelines and registration dossiers, CTD format, project management, lifecycle management, price and reimbursement, and regulatory submissions will be instrumental in driving our success.

Required Skills and Qualifications
  • A Master's degree in Pharma Industry or Regulatory Affairs Management
  • Minimum 4 years' experience in the field
  • Strong analytical skills, attention to detail, and ability to manage multiple tasks and priorities
Benefits

At QbD Group, we value our employees' contributions and celebrate their achievements. We offer a dynamic and supportive work environment, opportunities for continuous learning and development, and a chance to be part of our global success story. Our promise to you includes job security, lasting connections, and a joyful community where you can be yourself.

We stand for JPEG: Joy in Partnership, going for the Extra mile to Get things done. If you're interested in this opportunity, please submit your CV and motivation letter. We look forward to welcoming you to our QbD family.



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