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Regulatory Affairs Manager
hace 2 meses
We are seeking a highly experienced Senior Regulatory Affairs Officer to join our team at QbD Group in Spain. As a key member of our regulatory affairs department, you will be responsible for ensuring compliance with pharmaceutical legislation and regulations.
With a strong background in regulatory affairs, you will have expertise in ICH guidelines, registration dossier, CTD format, and lifecycle management. Your experience in project management roles will also be valuable in this position.
As a Senior Regulatory Affairs Officer, you will work closely with our team to develop and implement regulatory strategies that meet the needs of our clients. Your excellent analytical skills, attention to detail, and ability to manage multiple tasks and priorities will make you an asset to our team.
The ideal candidate will have a Master's degree in Pharma Industry or Regulatory Affairs Management and a minimum of 4 years' experience in the field. You will be both client-oriented and results-driven, with a strong commitment to delivering high-quality work.
What We Offer- A competitive salary package tailored to individual needs, considering local laws and regulations: €60,000 - €80,000 per annum
- A sustainable career with job security, lasting connections, and continuous learning opportunities
- A chance to be part of our global success story as an award-winning company
- A joyful community where you can grow and develop as a unique individual
