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Junior Pharmaceutical Consultant

PQE Group

Barcelona

Presencial

EUR 50.000 - 70.000

Jornada completa

Hace 6 días
Sé de los primeros/as/es en solicitar esta vacante

Descripción de la vacante

A leading consulting firm in pharmaceuticals is seeking a Junior Pharmaceutical Consultant in Barcelona. You will resolve compliance issues, draft validation deliverables, and ensure GMP compliance. Candidates must have a Bachelor’s Degree in Chemical Engineering and fluency in Spanish and English. Apply to join a dynamic team and work on international projects.

Formación

  • Bachelor’s Degree in Chemical engineering is a must.
  • Fluency in Spanish and English at least B2 level is required.
  • Willingness to travel is necessary.

Responsabilidades

  • Resolve fundamental Computer System Validation compliance issues.
  • Draft and review validation deliverables including Validation Plan and Test Plans.
  • Plan measures to maintain GMP compliance.

Conocimientos

Fluent in Spanish
Fluent in English
Risk assessment
GMP compliance

Educación

Bachelor’s Degree in Chemical engineering
Descripción del empleo
Overview

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. Working in a consulting reality, PQE Group will give you the chance to work on projects for the most important national and international pharmaceutical companies.

Due to a constant growth, PQE is looking for a Junior Pharmaceutical Consultant to support one of our clients in Barcelona, Spain.

Responsibilities
  • Resolution of fundamental Computer System Validation compliance issues on assigned projects
  • Drafting and review of main validation deliverables such as Validation Plan, User Requirement Specification, Functional Design Specification, Risk Analysis, Test Plans (FAT, SAT, DQ, IQ, OQ, PQ), Test & Validation Reports
  • Planning and coordinating measures to maintain GMP compliance
  • Ensure all project-related issues and deviations are recorded, approved and dispensed accordingly (including ensuring proper deviation report preparation and approval)
  • Collaboration in project teams and close interaction with clients, team members and external stakeholders
  • Performing of risk assessments
Qualifications
  • About you :
  • Bachelor’s Degree in Chemical engineering (must have)
  • Fluent in Spanish and English (at least B2)
  • Availability to travel
Next Steps

Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there is a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome from the Hiring Manager interview, the recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process.

Working at PQE Group

As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

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