BlueReg recrute des professionnels enthousiastes, à tout niveau d'expérience et d'expertise en Affaires Réglementaires Pharmaceutiques

Blue Reg recrute au Royaume-Uni et en France. Nous recherchons des professionnels enthousiastes ayant une expérience européenne en Affaires Réglementaires pharmaceutiques.

Rejoignez nos équipes hautement qualifiées constituées de plus de 50 consultants aux profils variés, mobilisés dans un fort esprit d’équipe pour répondre aux besoins et attentes de leurs clients. BlueReg assure des prestations à très forte valeur ajoutée pour plus de 100 clients, allant de la multinationale à la petite start-up , pour des entreprises innovantes comme pour des « génériqueurs ».
Vous souhaitez intégrer une équipe dynamique, tournée vers le succès et la croissance? Postulez en envoyant CV et lettre de motivation à ou cliquez sur le lien ci-dessous.



Pourquoi BlueReg?

Nous sommes une société en forte croissance qui, par conviction, investit dans le développement et la formation de ses collaborateurs. Chez BlueReg vous aurez l’opportunité de renforcer vos connaissances sur de multiples de domaines tout en consolidant vos expertises spécifiques. Notre équipe est chaleureuse et nous accordons beaucoup d’importance à la qualité de vie au travail ainsi qu’à l’équilibre vie personnelle – vie professionnelle. Chez BlueReg, vous travaillerez en mode projet au sein d’équipes multiculturelles, acquérant ainsi une expérience « globale ».


Que disent les collaborateurs?

‘’BlueReg is a varied team of experienced professionals, with a strong investment in the development of employees, providing a supportive and encouraging environment to continuously improve expertise, learn from one another and evolve to meet the needs of clients and the regulatory environment. BlueReg strives for excellence and it is a pleasure to be part of such an ambitious, enthusiastic and nurturing company.’’

Nicole consultant

‘’BlueReg is a dynamic and flexible company that gives excellent opportunities for consultants to develop in an enjoyable environment.’’

Justine consultant

‘’When I joined Blue-Reg, what particularly impressed me was the wide range of expertise covered by its employees. Each participant occupies a well-defined place, there is no sense of competition but solid teamwork in which all members are invested in one main goal: to permanently deliver quality services to their clients. Blue-Reg is a big family where I feel I play an important role, I am well-supported, continually trained and my work is acknowledged for its true worth. Blue-Reg’s dynamism, wide expertise, ever increasing development and good customer satisfaction are its principal strengths. I am proud to work for such a challenging company!’’

Sylvie consultant

Our offers

Director of Business Development to join our expanding international Group UNITED KINGDOM ; FRANCE - Paris and Sophia Antipolis

BlueReg Group is a consultancy organisation offering strategic advice and hands-on outsourcing solutions to life science companies
through the entire lifecycle of their products.

BlueReg was founded in 2011 and, since then, has experienced significant year-on-year growth. It today employs more than
50 full-time employees and has worked with over 100 clients ranging from large multinationals to small start-up pharmaceutical companies.

In the context of its continued growth, BlueReg is currently seeking an experienced Director of Business Development to develop
and head the BD department.


Key duties and responsibilities are summarized below:

  • Sets up and implements plans to develop new business opportunities at existing accounts, to acquire new clients and capture new business opportunities
    in line with BlueReg ambition
  • Participates in pricing and proposal activities for opportunities as appropriate
  • Leads client presentations, RFP responses and bid defence meetings
  • Closes major new project deals with clients in coordination with BlueReg CEO
  • Provides general intelligence on the life sciences environment and key competitors
  • Establishes, cultivates and grows client relationships at the appropriate levels
  • Presents and promotes the company services and participates in international conferences and meetings with clients, external vendors or advisors.



  • Minimum 10 years relevant experience in a similar role;
  • Minimum 5 years’ experience in Life Sciences (Pharma/Biotech), ideally with a CRO background and/or Consulting environment experience;


Education and skills

  • Bachelor’s degree in life sciences required. MBA preferred;
  • Fluent in English and French; ideally native English
  • Outstanding verbal and written communication skills;
  • Willingness to travel mainly in Europe and in the US
  • Strong presentation skills;
  • Strong leadership skills and ability to positively influence both customers and team members within BlueReg;
  • Ability to be a team player and/or work independently;


Please send a copy of your CV and a cover letter to


Senior Consultant, Regulatory Affairs UNITED KINGDOM – London

BlueReg Group is a consultancy company specialized in Development, Regulatory Affairs, quality management
and Pharmacovigilance for the Pharmaceutical Industry.


Based in Paris, Sophia Antipolis and London, BlueReg Group has over 100 clients ranging from large multinationals to small start-up companies,
from innovators to generic companies.


We are recruiting:
Senior Consultant, Regulatory Affairs (EU and UK/Ireland)

  • Your key duties and responsibilities:
    Is a source of regulatory expertise in the development, registration and post-licensing
    activities of pharmaceutical products
  • Project management activities
  • People management / Review of work of junior personnel and BlueReg partners
  • Ensures high quality and on time delivery of consulting services to clients.
  • Contributes to the effective functioning and to the business growth of BlueReg EU


Your profile :

  • Pharmacist, Life Sciences Graduate, ideally with post-graduate qualification.
  • Sound knowledge of pharmaceutical regulations and guidelines.
  • Significant regulatory affairs experience including a successful track record in the registration of medicinal products
  • A least 10 year experience in the pharmaceutical industry, broadly based Regulatory


Affairs experience, including a successful track record in the registration and maintenance of pharmaceutical products within Europe and UK/Ireland.

You have excellent written and verbal communication skills, good organisational and analytical skills. You are fluent in written and spoken English.

This position is based in High Wycombe, UK.


Regulatory professionals Work with BlueReg

BlueReg is recruiting and we are looking for enthusiastic Regulatory professionals with experience in EU Regulatory Affairs.

BlueReg was founded in 2011 and since then has seen significant year-on-year growth.

It comprises a team of more than 40 highly experienced full-time employees who have proven track records within the pharmaceutical industry.

BlueReg has over 100 clients ranging from large multinationals to small start-up companies, from innovators to generic companies.

If you want to join this dynamic and dedicated team whose members are committed to working together to provide clients with a high quality service,
please send a copy of your CV and a cover letter to


Découvrez notre dernier white Paper

Voir plus