QA Specialist

JR Spain; Zaragoza; Presencial; EUR 35.000 - 55.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company in Zaragoza is seeking a Quality Assurance Specialist to manage quality procedures and support manufacturing facility expansion. The ideal candidate will have over 3 years of experience in a quality department, strong organizational skills, and fluency in Spanish and English. This is a crucial role ensuring compliance with quality standards during a phase of significant growth.

Formación

• 3+ years of experience in a Quality department focused on Aseptic processes.
• Strong awareness of quality issues.
• Basic knowledge of regulatory requirements.

Responsabilidades

• Support the development of projects for facility expansion.
• Manage change controls procedures and documents.
• Approve/verify documentation related to the Quality Management System.
• Support preparation of internal audits and inspections.

Conocimientos

Fluent Spanish

Fluent English

Attention to details

Organizational skills

Descripción del empleo

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Exciting Opportunity: Quality Assurance Specialist in the Pharma Sector

Job Description: We are thrilled to announce an incredible opportunity for a Quality assurance in the pharmaceutical sector. Our client a top leading pharmaceutical company is currently living an expanding moment with a new facility and Oxford is hiring dynamic individual to join our team.

Responsibilities:

• Support the development and implementation of the projects for manufacturing facility expansion.
• Ensure that the company projects objectives and policies are consistent with GMPs.
• Manage (hands on) change controls procedures and documents.
• Handle the deviations as Certified Lead Investigator or QA Approver.
• Approve/verify the documentation (specifications, sampling and control methods, QC procedures, protocols, among others).
• Guarantee the correct document lifecycle management (paper and electronic system).
• Update the lists of documents related to the Quality Management System based on the indications of the reference SOPs.
• Collaborate in drafting a new version of Site Master File and/or Validation Master Plan.
• Support the preparation and execution of internal audits and Health Authorities inspections.
• Assure the execution and the proper documentation of training activities in the site.
• Support technological and organizational interventions aimed at the improvement of manufacturing processes in terms of quality, productivity and costs and the optimization of the resources relating to the site.

Requirements:

• Spanish, English fluently, verbally and in writing
• 3+ years of experience in a Quality dept. (Aseptic)
• Strong affinity with and awareness of quality issues
• Good organizational skills including attention to details.
• knowledge of quality system (GMP)
• Basic knowledge of regulatory requirements

How to Apply: Don't miss out on this amazing opportunity! Submit your application. Join us in this exciting phase of growth in the pharmaceutical sector!

We look forward to welcoming a passionate and skilled individual to our team!