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Rebecca BOLOGNINI

ROUEN

En résumé

Natural sciences degree, in chemistry, focused on organic chemistry, and analytics. Any professional experience in Cosmetic and Pharmaceutical business, Regulatory Affairs under cGMP/cGLP, EU GMP, ISO regulated environment. I have the proven capacity as regulatory affairs manager for submission DMF, SMF to various regulatory authorities, as laboratory Engineer within Quality Assurance & Quality Control for various systems. By that I mean, I am highly adaptable, due to my capacity to learn quickly. Also, I like facing challenges and don’t shy away from adversity. The through line of my professional career is continuous improvement in regulatory activities.

Specialties
- Regulatory Affairs / Quality Systems / Quality Assurance
- R&D/ Manufacturing
- Quality Control / Analytical Development
- Intellectual Property Industrial
- Equipment & Facilities Qualification
- Cleaning & Process Validation
- Internal Auditing Programs
- Suppliers Evaluation
- Technical Assessment

http://www.linkedin.com/in/rebeccabolognini

Mes compétences :
R&D
Chimie analytique
Qualité
Gestion de projet
Galénique
Industrie pharmaceutique

Entreprises

  • VALDEPHARM - FAREVA - - Regulatory Affairs Manager

    2010 - maintenant
  • ASSYSTEM - Consultant at Sanofi Pasteur

    Courbevoie 2009 - 2010
  • Council for Scientific and Industrial Research, CSIR in Pretoria - Visiting scientist

    2009 - 2009
  • ROBERTET - Trainee Engineer in Analytical Chemistry

    GRASSE 2007 - 2008
  • CENTIPHARM-AXYNTIS - Trainee Technician in Analytical Chemistry

    2006 - 2007
  • GALDERMA - Medicinal Chemistry Technician

    Courbevoie 2005 - 2006
  • L'OREAL - Research Chemical Technician

    PARIS 2001 - 2005
  • AVENTIS ANIMAL NUTRITION - Trainee Technician: Process Chemistry

    2000 - 2001

Formations

Réseau

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