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Quality Assurance Technician – Pharmaceutical

Centrient Pharmaceuticals · Santa Perpètua de Mogoda

Junior 🇬🇧 English
SAP stability studies

Job description

About the role

We are seeking a Quality Assurance Technician to support our pharmaceutical manufacturing operations. The role involves ensuring product quality, compliance with GMP standards, and continuous improvement of quality processes.

Key responsibilities

  • Review and sign Certificates of Analysis for customers, including CSO checks.
  • Test and release preparation shipments.
  • Conduct internal quality audits and promote good housekeeping.
  • Prepare reports on quality issues of manufactured products.
  • Manage GMP training programs across departments.
  • Control documentation for investigations, process changes, and recoveries.
  • Develop and coordinate validation and re‑validation plans, supervise stability studies.
  • Track periodic calibration of plant instrumentation.
  • Prepare annual product reviews and update SOPs.
  • Maintain quality IT systems such as SAP and VMPKey.
  • Represent QA on projects, committees and sub‑committees.

Required profile

  • Bachelor’s degree.
  • Fluent in English and Spanish.
  • Minimum 2 years of experience in a similar QA role.
  • Knowledge of audit procedures and quality control, especially OOS handling.

Required skills

  • SAP (quality module).
  • Validation planning and execution.
  • Stability study coordination.
  • Instrumentation calibration.
  • Good Manufacturing Practice (GMP) compliance.
  • Out‑of‑specification (OOS) management.

What we offer

  • Local contract in a dynamic, operational environment.
  • Flat organization with high freedom and responsibility.
  • Opportunities for personal growth and cross‑functional collaboration.

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Published 2 months ago

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Centrient Pharmaceuticals

Santa Perpètua de Mogoda