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Generics International RA ¿Dónde vas a trabajar? Multinational Generic Pharmaceutical Company Descripción Reviewing Marketing Application Authorization (MAA) dossiers and liaising with the RA department at the company Headquarters in India. Supporting...

  • Generics
  • International RA

¿Dónde vas a trabajar?

Multinational Generic Pharmaceutical Company

Descripción

  • Reviewing Marketing Application Authorization (MAA) dossiers and liaising with the RA department at the company Headquarters in India.
  • Supporting existing and potential clients with regulatory/technical information on Hetero´s products.
  • Preparing and submitting dossiers to Health authorities in EU countries using national and decentralized procedures.
  • Contacting European Health Authorities to follow up on submissions.
  • Contacting European customers to elaborate RA strategies and coordinate submissions.
  • Reviewing and submitting response documents to deficiency letters of Health Authorities.
  • eCTD publishing.
  • Ensuring adequate maintenance of the dossiers: PSUR submissions, variations, renewals...
  • Keeping up to date with the latest regulatory requirements in the region.
  • Performing selected pharmacovigilance activities.
  • Providing support for the elaboration of quality agreements and for product release.
  • Proposing, elaborating and implementing new standard operation procedures.

¿A quién buscamos (H/M/D)?

  • Education to a degree level in Pharmacy or a life science.
  • At least 5 years' experience in the Regulatory Affairs Department of a pharmaceutical company, preferably with generic medicinal products.
  • Experience with European MA procedures (DCPs) will be valued.
  • Experience with procedures in European Non-EU countries, i.e. Israel, Serbia & Canada will be valued.
  • Experience with Pharmacovigilance and Quality Assurance will be valued.
  • Experience with eCTD software will be valued.
  • Good knowledge of current European regulations on the registration of medicinal products. Knowledge of GMP and Pharmacovigilance is a plus.
  • Fluency in English, both written and spoken. Computer skills at user's level.
  • Effective teamwork, with excellent communication and good organization skills; a flexible and enthusiastic approach to work, using your knowledge to solve technical issues. A customer-friendly attitude and the ability to meet demanding deadlines are also essential.

¿Cuáles son tus beneficios?

  • Contract of Employment: full-time permanent position.
  • Benefits package (health insurance, ticket restaurant, complimentary fruit/coffee/snacks).
  • Hybrid work model: 1 day/week of home office.
  • Flexible schedule (8-10am to 4-6pm)
  • Young, positive team culture & engaging interactions within a multicultural team.
  • Teambuilding activities.

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