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Viatris

Comunidad Valenciana

Presencial

EUR 10.000 - 30.000

Jornada completa

Hace 30+ días

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Descripción de la vacante

An established industry player in pharmaceutical manufacturing seeks a Senior Validation Technician to lead process, cleaning, and transport validations. This pivotal role involves preparing validation protocols, ensuring compliance with quality standards, and collaborating with various departments to enhance operational efficiency. With a commitment to quality and customer care, this position offers a dynamic environment where your expertise will directly impact the success of diverse projects. If you are a proactive problem solver with a strong background in quality assurance, this is an exciting opportunity to make a significant contribution to a forward-thinking organization.

Formación

  • Minimum of 7 years in Quality Assurance Systems and Validation.
  • High level of English and degree in Sciences or Pharmacy.

Responsabilidades

  • Follow the General Validation Plan and prepare validation protocols.
  • Ensure compliance with Quality Directives and manage change control.

Conocimientos

Teamwork
Proactivity
Problem Solving
Communication Skills
Leadership Skills
Organization and Planning
Observation Skills

Educación

Degree in Sciences
Degree in Pharmacy

Herramientas

SAP
Quality Systems
Validation
Drug Analysis
Production Processes

Descripción del empleo

Senior Validation Technician (Process, Cleaning and Transport)

FAMAR is a European provider of pharmaceutical manufacturing and development services (CDMO) with a legacy of 75 years of technology expertise.

Building on its experience, FAMAR is a reliable partner to deliver flexible solutions, from development to production and distribution. Continuity and customer care are the cornerstones of FAMAR’s long-term business-oriented partnership.

Through the commitment of 1800 employees worldwide, and with a network of 6 production sites in Europe, FAMAR supplies a wide range of more than 1800 products in a variety of dosage forms, in 80 international markets.

Mission

  • Follow the General Validation Plan and the validation planning established for the Plant.
  • Undertake process, cleaning and transportation validations in accordance with the NCF and the Group's Quality Directives.
  • Prepare validation protocols and reports, as well as the necessary documentation to develop the Plant validation program.
  • Guarantee the achievement of validations in accordance with the NCF and the Group's Quality Directives.
  • Plan for each element to validate the resources, necessary actions, responsibilities and documentation to be generated for its achievement.
  • Contact the departments involved, for the correct development of the process validation, cleaning or transportation.
  • Prepare process validation, cleaning or transportation protocols for each element to be validated.
  • Prepare reports with the validation results.
  • Write, supervise and keep updated the procedures linked to your activity and ensure their application.
  • Periodically prepare reports on your area of competence.
  • Evaluate and manage change control requests in your area of responsibility.
  • Preparation and participation in audits / inspections by clients or official organizations.
  • Participate in the management of Quality aspects of Clients / Projects (as project manager or as Quality batch manager in a project).
  • Participate in the evaluation and improvement of the Quality System in the Site.

Requirements

  • Education: Degree in Sciences or Pharmacy.
  • Languages: High level of English.
  • Professional Experience: Minimum of 7 years in Quality Assurance Systems and Validation with senior role.
  • Additional knowledge: SAP, quality systems, validation, drug analysis and production processes.

Required Profile

  • Ability to work as a team.
  • Proactivity and problem solving.
  • Results-oriented capacity.
  • Communication and leadership skills.
  • Organization and planning skills, rigor in action.
  • Good observation skills.

Location

Seniority level: Mid-Senior level

Employment type: Full-time

Job function: Production, Quality Assurance, and Manufacturing

Industries: Pharmaceutical Manufacturing

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