16 jobs voor regulatory affairs manager gevonden

As the successful Regulatory Affairs Specialist, you will have the following responsibilities:

• Play a key role in the regulatory information flow and follow-up on registration & compliance projects focussing on Europe
  
  
• Collect needed scientific data, prepare regulatory & risk assessments, registration dossiers, MSDS, and support label instructions for new and existing products within the aftermarket portfolio
  
  
• Follow-up on legislation and guidelines related to BPR, veterinary medicines and hygiene aftermarket in Europe
  
  

In This Role You Will Have Regular Contacts With

• Aftermarket Product Management, Regulatory Affairs & R&D colleagues (internal)
• Regulatory Authorities (external)
• Quality departments (internal)
• Contract labs and consultants (external)

As the successful Regulatory Affairs Specialist, you will have the following responsibilities:

• Play a key role in the regulatory information flow and follow-up on registration & compliance projects focussing on Europe
  
  
• Collect needed scientific data, prepare regulatory & risk assessments, registration dossiers, MSDS, and support label instructions for new and existing products within the aftermarket portfolio
  
  
• Follow-up on legislation and guidelines related to BPR, veterinary medicines and hygiene aftermarket in Europe
  
  

In This Role You Will Have Regular Contacts With

• Aftermarket Product Management, Regulatory Affairs & R&D colleagues (internal)
• Regulatory Authorities (external)
• Quality departments (internal)
• Contract labs and consultants (external)

Functieomschrijving.Nitto Belgium zoekt een medewerker Regulatory Affairs die zich specialiseert in chemical substance management.

De Regulatory Affairs Officer werkt mee in het Regulatory Affairs team, bestaande uit 13 personen dat verantwoordelijk is voor de ondersteuning van de global registration activiteiten...

In een full continue productie proces produceren zij verschillende chemische producten die worden gebruikt in uiteenlopende industrieën, zoals de productie van rubber, kunststoffen, coatings,.Voor hen zijn wij op zoek naar een master chemie die zal instaan voor de "Regulatory Affairs".

In this role, you will oversee quality assurance and regulatory affairs activities within our QARA department, staying ahead of regulatory changes, managing registrations, engaging with authorities, implementing ISO standards, and overseeing our quality management system You will provide strategic leadership to our team, ensuring compliance with relevant regulations and standards while driving continuous improvement initiatives..

Je assisteert het regulatory team bij het opstellen en opvolgen van product veiligheidsinformatiebladen en gerelateerd datamanagement..Je rapporteert aan de Manager Regulatory Affairs EMEIA. .

Door groei, willen zij hun gemotiveerd en competent team van de registratieafdeling versterken met een Regulatory Affairs Officer. Nauwe samenwerking met verschillende afdelingen op de hoofdzetel (Sales, Quality, Finance, Logistiek).

In this position, you will join our Regulatory affairs team and report to the Regulatory affairs manager:

• You are participating to the elaboration of risk assessments for human health, environment, animal health, dietary risk mainly for biocidal products.
• You are responsible for preparing, submitting and following up the registration dossiers for biocides, detergents… throughout the world.
• You stay up-to-date regarding new registrations, legal requirements and procedures.In addition, you manage our database and documentation.
• You maintain close contacts with authorities, external and internal stakeholders such as distributors, sales department, marketing, R&D, microbio ad phys-chem lab…

Company:

Science Talents is part of House of Talents, an international HR services group specialized in bottleneck professions.You will be working in a no-nonsense environment where team spirit, drive and learning moments are key.

We are very open and communicative go-getters who are keen on results and quality.

To further strengthen our growth, we are constantly looking for new colleagues within Project Staffing.

Rapportage aan de Regulatory Affairs Manager.Beheer van de database en documentatie.Verantwoordeljik voor de voorbereiding, indienen en opvolgen van productregistratie.Je volgt nieuwe registraties, wettelijke vereisten en procedures op.

Je werkt samen met R&D, wereldwijde regelgevende collega’s.Volgende taken liggen binnen jouw verantwoordelijkheid:Het samenstellen, aanvullen en actualiseren van registratiedocumentenNauwe samenwerking met Sales, Marketing en QA om de wettelijke verplichtingen na te levenBij de opstart van een nieuw product hou je mee de regelgeving in het oogJe gaat confidentieel te werk en zorgt dat alle verplichte info voorzien isUp to date houden van (toekomstige) veranderingen inzake medische toestellen en het voorzien van pro actief advies om de procedures en systemen aan te passen

Taken en verantwoordelijkheden:..

De verantwoordelijkheid dragen over laboratoriumontwikkelingen, zoals het creëren van testmethoden en het verkennen van nieuwe technologieën..Sterke relaties opbouwen met Sales, Regulatory Affairs, Productie en collega’s verspreid over heel Europa..

As a Sustainability Manager you’ll be supporting the development and implementation of the organizations’ corporate Sustainability strategy;.You’ll be leading and coordinating strategic sustainability assessments such as the double materiality assessments, EU Taxonomy assessment, carbon modelling exercise, etc..

Conduct internal audits and provide guidance regarding best practices and continuous improvement..Support core quality systems including root cause analysis, CAPA, non conformance, chance control, and risk management, as well as control of documentation and records..

Onder leiding van de Director Product Development werk je samen met collega's die zich richten op Product Management, Packaging Design en Regulatory Affairs.Jouw focus ligt op de ontwikkeling van de chocoladeproducten zelf.