Emplois actuels liés à Regulatory Affairs - Antwerp - Michael Page
-
Regulatory Affairs Consultant IVD
il y a 7 jours
Antwerp, Belgique Regulatory affairs Temps pleinQarad Belgium, The Netherlands Regulatory affairs Table of Contents Qarad, part of the QbD group, is a fast-growing consultancy company assisting manufacturers of In Vitro Diagnostics (IVD) and Medical Devices (MD) in coping with European and other regulations. Our objective is to provide manufacturers with practical solutions in the...
-
Associate Director/Director Regulatory Affairs
il y a 7 jours
Antwerp, Belgique Regulatory affairs Temps pleinRA The UK Regulatory affairs Table of Contents The UK team of the international QbD group, is a specialist regulatory and pharmacovigilance consultancy company. Our services consist in providing consultation throughout product development, regulatory approval, market launch, and into life cycle management. We have been offering...
-
Associate Director Regulatory Affairs
il y a 7 jours
Antwerp, Belgique Regulatory affairs Temps pleinRA Austria Regulatory affairs Table of Contents QbD Austria , part of the international QbD group, is a young and growing consulting company offering services and training on regulatory affairs, regulatory compliance, business organization and quality assurance in the pharmaceutical, food supplement and medical device industry. Our...
-
Regulatory Affairs Expert
il y a 7 jours
Antwerp, Belgique Telenet Temps pleinYour team The Regulatory Affairs Expert is a member of the Tribe Legal & Regulatory. Under the supervision of the Director Regulatory & Compliance, the Regulatory Affairs Expert provides regulatory advice, representation and support. This in relation to a broad range of regulatory topics, focused on the services and products of Telenet and companies in...
-
Medical Device/IVD Software Specialist
Il y a 5 mois
Antwerp, Belgique Software validation Temps pleinSoftware Belgium Software validation Table of Contents Do you have in addition to your passion for regulatory affairs, also an affinity with IT? Would you like to be a part of QbD’s Software & Services Division and specialize in Medical Device Software Validation? Then apply now and become a member of our growing QbD team! What do...
Regulatory Affairs
Il y a 3 mois
We are looking for a Regulatory Affairs Specialist to join an international pharmaceutical company specialised in veterinary medicines and feed additives.
Our client is a fast- moving large-scale pharmaceutical company with over 3000 employees and an international presence in more than 20 countries. They have a significant impact on the Life Sciences sector and are renowned for their commitment to innovation, development and quality. Strong growing ambitions are expected over the 5 coming years.
As a Successful Regulatory Affairs Specialist - Veterinary products and Feed Additives, you will have the following responsibilities:
- Prepare various regulatory documentation for veterinary products and feed additives.
- Prepare registration dossiers for veterinary products and feed additives.
- Submit registration documentation to competent authorities worldwide & monitor progress.
- Analyse, understand and share relevant regulatory trends related to the Veterinary medicines and the feed additives (Focus on EU & UK).
- Manage the label design of the veterinary products and feed additives.
- Support safety department in their materials preparation.
As a Successful Regulatory Affairs Specialist - Veterinary products and Feed Additives, you have the following profile
- A degree in Veterinary, Life Sciences, Pharmacy, or a related field.
- 1-3 years of experiences in a previous Regulatory Affairs position is a plus.
- Knowledge of EU & UK Regulations within the healthcare industry.
- Excellent communication skills - both oral and written - to liaise with various departments and regulatory bodies.
- A strong eye for detail, ensuring all regulatory documents are accurate and complete.
- Capacity to work independently with the ability to analyse and interpret complex regulatory documentation.
- A strong cooperative mindset to liaise and collaborate with the different departments (Safety, Clinical, Marketing ).
- Fluent in English, Dutch being a plus.
- Willingness to work at the Antwerp office most of the time.
As a Successful Regulatory Affairs Specialist - Veterinary products and Feed Additives, you will have:
- A competitive fix salary coupled with interesting benefits package
- A vibrant and innovative work culture in the Life Sciences department.
- Opportunities for professional development within a growing international pharmaceutical company.
- Working in a prominent location in Antwerp.
Veterinary, Dutch Language, Liasion duties, Attention to detail, Health & Safety, VOS, Documentation, Registration, Life Science, Communication, Regulatory Affairs, Health System, Cooperatives, Marketing, Veterinary, Safety Department, Regulatory Bodies, Regulation, Pharmacy, Design