Anunciado 22 de octubre
Tipo de jornada
Completa
Tipo de contrato
Otros contratos
Salario
Salario sin especificar
Estudios mínimos
Sin especificar
Nivel
Sin determinar
Número de vacantes
1
Tags Relacionados
Descripción del empleo

We are hiring for a Scientist to incorporate to our Elemental Analysis department. The person Will be assigned the following responsibilities:



  • Management and execution of ICP-MS and AAS studies that are carried out for Quality Control and Stability Studies of pharmaceutical, veterinary, health and cosmetic products.

  • Management, execution and review of tests by ICP-MS and AAS for development studies, validation and / or method transfers and routine sample analysis.

  • Design, supervision, review and execution of method validation by ICP-MS and AAS.

  • Drafting and review of related documentation (SOP, protocols, guides, reports, etc.).

  • Direct involvement in all technical aspects related to analytical methods, problem solving, transfer of analytical methods, etc.

  • Management and writing of Incidents, deviations, OOS and CAPAs.

  • Management and organization of the qualification of the teams assigned to the department.

  • Management of studies and results through LIMS system.

  • Contact with the Quality Control and Stability departments of the company

  • Work under GMP and GLP compliance.



Requisitos mínimos

We are looking for a candidate with:



  • University degree: Chemistry or Pharmacy Bachelor's.

  • Some experience in a Quality Control department in the Pharmaceutical industry or Third-Party Analysis Company (CRO).

  • Experience in management, design and performance of physicochemical tests of active ingredients, drugs, cosmetics, ...

  • Experience in working with computerized systems.

  • Experience in working under GMP and GLP standards.

  • Knowledge of pharmacopoeias, guidelines, regulations that apply in the field of GMPs.

  • Advanced English level is a must.

  • Knowledge of the ICH Q3D guideline will be valued.



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