Regulatory Affairs Officer
STADA Arzneimittel
About EGEG is a Purpose driven company: at the core of everything we do, we aim to Care for People´s Health as a Trusted Partner.EG is the largest pharmaceutical company in Belgium.With an offering for just about every therapeutic area, we are the market leader in generic medicines and the biggest OTC company in Belgian pharmacies.Most of our medicines and food supplements are produced in Belgium. We currently have 180 employees and continue to invest in:
Our culture is characterized by the strong commitment of our employees. Internally, we are called “MEP’s”: Motivation – Energy – Passion are therefore qualities that we look for in every potential new employee to help strengthen our culture.We are part of the Stada Group and share the values Integrity, Agility, Entrepreneurship and One Stada.Do you have a strong MEP level? Are you entrepreneurial and would you like to work for the largest and fast-growing pharmaceutical company in Belgium? Then EG might be the perfect employer for you.Regulatory Affairs Officer (f/m/x)Brussels | BE | Full Time | PermanentAbout the Pharmaceutical Affairs DepartmentPharmaceutical Affairs (PA) Department consists of Regulatory Affairs, Quality Assurance, Medical Affairs and Pharmacovigilance. The department ensures that our products are produced and delivered to customers according to the highest quality and safety standards and complying with the local and EU regulatory requirements.About your roleThe Regulatory Affairs Officer (RAO) is responsible for managing the lifecycle of the medicines from the preparation of the registration dossier, including the follow-up and finalization of new registrations, the preparation to market access, compilation, submission, and follow-up of variation dossiers in Belgium and Luxembourg.Also managing the lifecycle of non-medicines (e.g. food supplements and medical devices) by preparing, compiling, submitting and following up the notification files in Belgium and Luxembourg.The RAO will provide administrative assistance to internal stakeholders (including Supply Chain Department, Sales and Marketing Department) and external customers (including regulatory authorities and professionals in the medical-pharmaceutical world) to ensure a smooth launch and continuity of the products on the market and good sales.This role is part of a team of 4 Officers and reports to the Regulatory Affairs Manager.How you can make an impactFollow up of new registration procedures until launchThe RA Officer is responsible for submitting, following up and finalizing registration procedures to obtain a marketing authorization as quickly as possible to be able to commercialize the product in Belgium and Luxembourg within the set time frame.Managing and maintaining registered corporate and non-corporate proceduresManaging existing corporate (DCP, MRP, CP) and non-corporate (NAT) registrations in Belgium and Luxembourg to guarantee the continuity of the supply of the products within the legislative framework. This includes the preparation, submission and follow-up of variations, renewals and notification dossiers. Also initiating, reviewing and approving changes to packaging materials (e.g. artworks).Keeping databases up-to-date (administrative)Taking care of the correct management of various internal and external databases to ensure permanent access to necessary information regarding the products.
Legislation, procedures and work instructionsAcquiring and maintaining knowledge with regard to national and European legislation, guidelines and the application thereof in procedures and work instructions within the framework of the general EG quality systemScientific supportProviding scientific support with regard to answering pharmaco-technological questions from patients, doctors, pharmacists and/or hospitals.Work closely together with colleagues from all other departments within EG: Supply Chain, Business Development, Sales and Marketing, Finance, …What we are looking forHow we care for you
More information about EG and what is to work for us? Visit orEG values and promotes its diverse culture, regardless of gender, age, social or ethnic origin, disabilities, religion, ideology or sexual orientation. We use the strength of our uniqueness to develop creative ideas, expand our experience and increase innovative strength. Our focus is on equal opportunities, respectful cooperation and the promotion of an inclusive working environment. We are looking forward to your application and welcome applications without a pharmaceutical background.
Belgique
Thu, 08 Aug 2024 02:55:24 GMT
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