Hikma Pharmaceuticals

Trainee, Technical Affairs Scientist

L'Oriental

CDI / Temps pleinSur site0–1 anMaster / Bac+5AnglaisProduction / IndustriePharmaceutique

L’essentiel du poste

Résumé par Postule AI

Hikma Pharmaceuticals is recruiting a Trainee, Technical Affairs Scientist for an on-site, full-time role in its Technical Affairs department. The role supports technology transfer, GMP documentation, process validation batches, deviation and CAPA follow-up, regulatory filings and routine production. Candidates should hold a Master's in Pharmaceutical Sciences, have 0-2 years of experience and be fluent in English.

Vos missions

  • Work on Quality Risk Management for the technology transfer of new products.
  • Prepare GMP documents to support the technology transfer of medicinal products (injectables).
  • Support the manufacturing of process validation and exhibit batches under Good Manufacturing Practices.
  • Support deviation reports for product-related issues and establish corresponding CAPAs.
  • Support the Regulatory Affairs team in filing new products in several markets.
  • Provide technical support to routine production and investigations.

Profil recherché

  • You hold a Master's degree in Pharmaceutical Sciences and are early in your career (0-2 years).
  • You are interested in GMP, quality risk management and injectable medicine manufacturing.
  • You communicate fluently in English and present information clearly.
  • You are responsible, proactive and comfortable working in a team.
  • You stay organized and can work under pressure to meet deadlines.

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Trainee, Technical Affairs Scientist

Hikma Pharmaceuticals is recruiting a Trainee, Technical Affairs Scientist (m/f) to join the Technical Affairs department on an on-site basis. The location listed is Hay Al Hikma II, Oriental, Morocco.

Hikma was founded over 40 years ago in Jordan with the purpose of providing high-quality and affordable medicines. In Portugal, the company employs more than 1,000 people and operates three manufacturing sites dedicated to injectable medicines.

Main Responsibilities

  • Work on Quality Risk Management for the technology transfer of new products.
  • Prepare GMP documents to support the technology transfer of medicinal products (injectables).
  • Support the manufacturing of process validation and exhibit batches, ensuring compliance with Good Manufacturing Practices.
  • Support deviation reports (product related) and establish the corresponding Preventive and Corrective Measures (CAPAs).
  • Support the Regulatory Affairs team in filing new products in several markets.
  • Provide technical support to routine production and investigations.

Candidate Profile

  • Master's degree in Pharmaceutical Sciences.
  • 0-2 years of experience.
  • Fluency in English, with strong presentation and communication skills.
  • Responsibility, proactivity and teamwork.
  • Organization and planning capabilities.
  • Ability to work under pressure and meet deadlines.

What We Offer

  • Initial and ongoing training within a dynamic and positive environment.
  • Professional development and career growth opportunities.
  • The opportunity to gain knowledge and best practices within a rapidly expanding international group.

Join us and help contribute to Better Health, Within Reach, Every Day.

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