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This job expired on 08/09/2026. It no longer accepts applications.
Quality Assurance Technician – Pharmaceutical
Centrient Pharmaceuticals · Santa Perpètua de Mogoda
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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Centrient Pharmaceuticals
Santa Perpètua de Mogoda
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