Quality Trainee

Uriach; Sant Cugat del Vallès; On-site; EUR 8,928 - 13,392; Full time

Job summary

A pharmaceutical company in Sant Cugat del Vallès is seeking a Quality Trainee to provide quality control services across the Spanish, Portuguese, and Italian markets. Key responsibilities include ensuring compliance with GMP/GDP standards, drafting SOPs for the Quality Department, and monitoring product analysis and stability studies. A degree in pharmacy, chemistry, or a related field is required, while fluency in Italian is a plus. This is an internship position offering valuable experience in quality assurance.

Qualifications

• Degree in pharmacy, chemistry, biology, food science and technology or similar.
• Fluent in Italian is a plus.

Responsibilities

• Ensure compliance with GMP/GDP standards for pharmaceutical products.
• Draft and update SOPs for the Quality Department.
• Write specifications in SAP QM.
• Monitor and execute product analysis according to regulations.
• Manage stability studies of all products.

Skills

Quality control

Regulatory standards compliance

SOP drafting

SAP QM

Fluent Italian

Education

Degree in pharmacy, chemistry, biology, food science, or similar

Job description

Quality Trainee

Join to apply for the Quality Trainee role at Uriach.

The trainee will provide quality control services for the Spanish, Portuguese and Italian markets.

Key Responsibilities

• Ensure and document compliance with GMP/GDP standards for pharmaceutical products, ISO 13485 for medical devices, ISO 22716, ISO 22000, and the applicable Directives/Regulations related to Uriach CHC products.
• Draft and update SOPs (Standard Operating Procedures) for the Quality Department.
• Write specifications in SAP QM according to regulatory registration or technical data sheets.
• Perform, monitor, and execute the analysis of all products in accordance with the applicable regulatory standards.
• Open non-conformities when appropriate and implement the corresponding corrective actions.
• Inform the CMO of any non-conformity.
• Participate in the execution and monitoring of the non-conformity indicator.
• Ensure the availability of samples from all batches, their custody, and proper storage conditions in the sample archive.
• Participate in the feasibility and development phase of products, establishing pre-stability requirements and evaluating them.
• Attend inspections, audits, and requests from health authorities.
• Collaborate in the monitoring of the general budget of the Department.
• Monitor and control the stability studies of all products.
• Manage the stability budget.
• Provide necessary information to the Supply, Innovation, or CHC ROW departments.

Requirements

• Degree in pharmacy, chemistry, biology, food science and technology or similar.
• Fluent Italian is a plus.

Seniority Level

Internship

Employment Type

Internship

Job Function

Quality Assurance

Industries

Wholesale Drugs and Sundries

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