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Quality Control Analyst

CHEMO pharmaceutical group

Castellón de la Plana

Presencial

EUR 30.000 - 45.000

Jornada completa

Hace 5 días
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Descripción de la vacante

A leading pharmaceutical group is seeking a Quality Control Analyst to perform physicochemical analysis of injectable products in Castellón de la Plana. The ideal candidate will have a strong educational background in chemistry and experience in laboratory settings, particularly with injectable products. This full-time position offers opportunities for professional growth and collaboration in a dynamic team environment.

Formación

  • 2+ years working in a laboratory, ideally with injectable products.
  • Fluent Spanish; medium level English is a plus.
  • Basic training in GMP.

Responsabilidades

  • Perform analysis of raw materials, intermediate products, and final products.
  • Collaborate in the transfer of analytical methods.
  • Carry out daily checks on the laboratory equipment.

Conocimientos

Analytical skills
Accuracy and reliability
Teamwork

Educación

FP II Chemistry
Basic Studies in Chemical Analysis

Descripción del empleo

Chemo Villaquilambre, Castilla and Leon, Spain

Quality Control Analyst

Overview :

Perform physicochemical analysis of injectable products.

Responsibilities :

  • Perform analysis of raw materials, packaging materials, intermediate products and final products.
  • Collaborate in the transfer of analytical methods.
  • Manage reagents, laboratory material, chromatographic columns, etc.
  • Sampling raw materials and starting materials.
  • Carry out the necessary daily checks on the equipment of the Physico-Chemical laboratory.
  • Contribute in the training of the new incorporations in the specific activities and functions of the position in which you are an expert.

Qualifications :

  • Education : FP II Chemistry or Basic Studies in Chemical Analysis.
  • Languages : Fluent Spanish, medium level English is a plus.
  • Experience : +2 years working in a laboratory, ideally with injectable products.
  • Specific knowledge : basic training in GMP.
  • Travels : not required.
  • Personal skills : Good analytical skills, accuracy and reliability, team worker.

Seniority level : Not Applicable

Employment type : Full-time

Job function : Quality Assurance

Pharmaceutical Manufacturing

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