This position is no longer open for applications

Are you looking to start or expand your career path in the pharmaceutical industry and develop your scientific skills? We have a unique opportunity for you to demonstrate your pharmaceutical expertise within the leading EU institution of medicines and pharmacology based in Amsterdam!

We are the exclusive recruiters for the interim positions at the European Medicines Agency (EMA). The EMA are the medical regulatory organisation responsible for public human and animal health throughout the European Economic Area. They are now looking for a Bilingual Regulatory Affairs Officer to join one of their teams on an 18 month temporary (Interim) contract.

You will predominantly provide regulatory and procedural advice to the EMA staff, Scientific Committees and other stakeholders throughout the medicinal products’ lifecycle. This is an exciting opportunity to join an institution that provides a truly international working environment where everyone is passionate about public health. Extensive training is provided where you will have the opportunity to expand your skills.

Your responsibilities will include:

• Provide timely regulatory advice in relation to development, evaluation and supervision of medicinal products for human use
• Undertake risk-based regulatory checks of documents to ensure compliance with Union legislation prior to distribution to scientific committees and/or the EC
• Support thorough and consistent interpretation and application of Union legislation by and within operational offices
• Regulatory support in relation to legislative proposals and implementation of new legislation in collaboration with relevant EMA functions
• Develop and/or update regulatory and procedural guidance and guidelines
• Support the effective optimisation of the regulatory framework with focus on process optimisation and quality assurance
• Effectively foster early awareness of staff and management of new/complex regulatory issues
• Proactively build and share regulatory knowledge within the office and across the Agency

Profile:

• Fluency in English and another EU language
• Proven experience in regulatory affairs of at least 3 years
• Good understanding through practical experience with European legislation framework underpinning regulation of medicinal products
• Proven experience within a healthcare, scientific, pharmaceutical or regulatory environment
• Studies in pharmacy or life sciences
• Experience of working in a multicultural environment

Fluency in English and at least one other EU language –Spanish, Czech, Danish, German, Estonian, English, French, Italian, Latvian, Lithuanian, Hungarian, Maltese, Dutch, Polish, Portuguese, Slovenian, Slovakian, Finnish, Swedish, Greek, Romanian, Bulgarian, Croatian, Norwegian, Icelandic

To apply, please send your CV in English and in Word format to Jessica Lara. If you have applied for any other languagematters vacancy there is no need to re-apply, as your CV will be considered for all vacancies that match your language skills and work experience.

languagematters is a multi-discipline, multilingual recruitment agency offering a wide range of bilingual jobs in the UK, the Netherlands and beyond. Our goal is to be the most valued, knowledgeable and indispensable recruitment partner in the language recruitment field.

We work constantly to provide equal opportunities for all, regardless of age, gender, ethnicity, social background, religion, disability or sexuality.

NB: Candidates must be eligible to work in the EU or hold a valid work permit. Please note that we contact successful candidates within 3-4 working days. languagematters is acting as an employment business in relation to this vacancy.