Ecy-810 - Quality Control Technician

AL Solutions; Sevilla; Presencial; EUR 30.000 - 40.000; Jornada completa

Descripción de la vacante

A leading Contract Development and Manufacturing Organization located in Spain is looking for a QC Technician. The role involves ensuring that raw materials and finished products meet quality standards, conducting laboratory analyses, and maintaining documentation in compliance with regulatory requirements. The ideal candidate has a degree in a scientific discipline and 1–3 years of experience in a GMP-regulated laboratory, with fluent Spanish being a requirement.

Formación

• 1–3 years of experience in a GMP-regulated QC laboratory, preferably within a CDMO or pharmaceutical environment.
• Hands-on experience with analytical instrumentation.
• Working knowledge of GMP and regulatory guidelines.

Responsabilidades

• Perform routine and non-routine analysis of raw materials and finished products.
• Conduct microbiological testing including bioburden and endotoxin.
• Accurately document all laboratory activities.

Conocimientos

HPLC

GC

Strong organizational skills

Documentation skills

Fluent Spanish

Educación

Degree in Chemistry, Pharmacy, Biotechnology, or related field

Herramientas

LIMS

Descripción del empleo

I am working with a leading CDMO (Contract Development and Manufacturing Organization) located in Spain, offering end-to-end services in the development and manufacturing of pharmaceutical and biopharmaceutical products. Our mission is to deliver high-quality, compliant, and innovative solutions to our clients across the globe.

Position Summary :

As a QC Technician, you will play a critical role in ensuring that raw materials, intermediates, and finished pharmaceutical products meet established quality standards and regulatory requirements. You will conduct laboratory analyses, maintain accurate documentation, and support continuous improvement in QC processes.

Key Responsibilities :

• Perform routine and non-routine analysis of raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV-Vis, FTIR, and wet chemistry.
• Conduct microbiological testing (if applicable) including bioburden, endotoxin, and environmental monitoring.
• Prepare reagents, solutions, and mobile phases as per SOPs.
• Ensure all testing is conducted in compliance with GMP, SOPs, and regulatory requirements.
• Accurately document all laboratory activities in logbooks, LIMS, and batch records.
• Participate in out-of-specification (OOS) investigations and support root cause analysis.
• Calibrate, maintain, and troubleshoot laboratory equipment.
• Support method transfers and validations as required.
• Assist in the review and revision of SOPs and QC documentation.
• Collaborate with cross-functional teams including QA, Production, and R&D.
• Maintain a clean and safe laboratory environment.

Qualifications :

Degree in Chemistry, Pharmacy, Biotechnology, or related scientific discipline. 1–3 years of experience in a GMP-regulated QC laboratory, preferably within a CDMO or pharmaceutical environment.

• Hands-on experience with analytical instrumentation (e.g., HPLC, GC).
• Working knowledge of GMP and regulatory guidelines (EMA, ICH, EU GMP).
• Strong organizational and documentation skills.
• Basic English proficiency (reading / writing technical documentation); fluent Spanish required.

Preferred Qualifications :

Experience in microbiological testing or biologics QC is a plus. Familiarity with LIMS and electronic laboratory systems. Knowledge of method validation and ICH guidelines.

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