×
Regístrese Aquí para solicitar empleo o publicarlo X

LLQuality Control Scientist III

Trabajo disponible en: 08001, Barcelona, Cataluna, España
Empresa: Veg Group
Tiempo completo puesto
Publicado en 2026-02-10
Especializaciones laborales:
  • Control de Calidad
Rango Salarial o Referencia de la Industria: 30000 - 50000 EUR Anual EUR 30000.00 50000.00 YEAR
Descripción del trabajo
Puesto: LL01-251118 Quality Control Scientist III

Current job opportunities are posted here as they become available.

LL01-251118 Quality Control Scientist III

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas:
Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Quality Control Scientist III

Qualifications:

  • Bachelor's Degree in Science.
  • Minimum of 8 years of experience in direct pharmaceutical quality control areas and regulatory operations.
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Must be proficient using MS Windows and Microsoft Office applications.
  • Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
  • Strong knowledge (according to related area).
  • Technical Writing skills and investigations processes.
  • Available to work extended hours, possibility of weekends and holidays.

Responsibilities:

Evaluate compendial changes from the different pharmacopeias.

Generate trend reports of investigations based on the company’s procedures.

Evaluate global documents against site‑specific procedures and update the site procedure accordingly.

Draft technical documents such as methods, specifications, method validation protocols and reports, method transfer protocols and reports, based on corporate policies, SOPs, compendial guidelines, ICH, DEA, and FDA regulatory guidance.

Generate required change requests for analytical documents and route documents for review and approval.

Conduct laboratory event/out-of-specification/out-of-trend investigations and close them on time.

#J-18808-Ljbffr
Tenga en cuenta que actualmente no se aceptan solicitudes desde su jurisdicción. Las preferencias de los candidatos son decisión del empleador o del agente reclutador.
Para buscar, ver y solicitar empleos que acepten solicitudes de su ubicación o país, toque aquí para realizar una búsqueda:
 
 
 
Busque más trabajos aquí:
(Ingrese pocas palabras para obtener mejores resultados)
Localización
Aumentar el radio de búsqueda (millas)

Idioma de la publicación
Categoría de empleo
Nivel educativo
Filtros
Nivel Educativo
Experiencia mínima requerida (años)
Publicado en los últimos:
Salario