Regulatory Affairs Technician

  • Location: Madrid 
  • Office-based position
  • Log term contract -18 months- directly hired by the Company with options for a permanent job 
  • Junior position 1.5-2 years of experience in Regulatory Affairs across different geographical territories and experience with OTC, nutraceuticals, generics and/or natural products. 
  • Travels: Not required.
  • 40 hours per week. 8-10 a.m. to 17-19 p.m. Monday to Friday 1 hour for lunch 
Responsibilities 
  • Define strategies for regulatory submissions of homeopathic products for obtaining and maintaining approvals for products. 
  • Participate in the preparation and/or review of documents together with the technical departments. 
  • Perform regular follow-up progress on regulatory submissions.
  • Coordinate internally the answers to the deficiency letters ensuring the timelines given by the Regulatory Agencies.
  • Provide local or regional training as appropriate to comply with international regulatory requirements.
  • Respond to health authority queries.
  • Participate in Scientific Advice meetings with regulatory agencies.
Profile 
  • Education: Degree in Chemistry, Pharmacy or life sciences.
  • Languages: Fluent Spanish and English, knowledge of other languages will be an asset.
  • Experience (years/area): Junior position 1-2 experience in Regulatory Affairs
  • Specific Knowledge: Knowledge of new legislation related to homeopathic.  
  • Travels: Not required.
  • Personal skills: Ability to work under pressure and with tight deadlines. Initiative, strong problem solving and negotiation skills.
     

Application form : Regulatory Affairs Technician

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Files must be less than 3 MB.
Allowed file types: txt rtf html pdf doc docx odt.

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