Freelance Qualified Person (Qp) – Pharmaceuticals

Uniletra Spain; Madrid; Presencial; EUR 50.000 - 70.000; A tiempo parcial

Descripción de la vacante

A leading company in pharmaceuticals is seeking a freelance Qualified Person (QP) based in the EU to ensure compliance and quality standards for batches produced by Chinese manufacturers. This role involves certifying batches, reviewing documentation, and supporting regulatory interactions. Candidates should have significant experience and understanding of EU GMP guidelines.

Servicios

Remote or on-site work depending on project

Competitive compensation

Formación

• Minimum 3 years of relevant experience in the pharmaceutical industry.
• In-depth knowledge of EU GMP guidelines, especially Annex 16.
• Strong ability to work independently.

Responsabilidades

• Perform batch certification and release in compliance with EU GMP.
• Review manufacturing and quality control documentation.
• Support for audits, inspections, and regulatory interactions.

Conocimientos

Attention to detail

Communication

Educación

Legally certified Qualified Person (QP) under EU Directive 2001 / 83 / EC

Descripción del empleo

Freelance Qualified Person (QP) – Pharmaceuticals Freelance Qualified Person (QP) – Pharmaceuticals

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We are currently seeking an experienced Qualified Person (QP) based in EU to collaborate on a freelance basis . As a QP, you will be responsible for the certification and release of medicinal product batches manufactured by Chinese pharmaceutical companies in accordance with EU requirements.

We are currently seeking an experienced Qualified Person (QP) based in EU to collaborate on a freelance basis . As a QP, you will be responsible for the certification and release of medicinal product batches manufactured by Chinese pharmaceutical companies in accordance with EU requirements.

Key Responsibilities

• Perform batch certification and release in compliance with EU GMP.
• Review manufacturing and quality control documentation.
• Ensure each batch meets specifications, regulatory approvals, and quality standards.
• Provide support for audits, inspections, and regulatory interactions when needed.
• Offer expert QA guidance throughout product lifecycle stages.

Requirements

• Legally certified Qualified Person (QP) under EU Directive 2001 / 83 / EC.
• Minimum 3 years of relevant experience in the pharmaceutical industry.
• In-depth knowledge of EU GMP guidelines , especially Annex 16.
• Strong attention to detail and ability to work independently.
• Excellent communication skills (English is a must).

We Offer

• Freelance collaboration on a regular basis
• Remote or on-site work depending on project
• Competitive compensation

Please send your CV and fee expectations to Thanks a lot.

Seniority level

• Seniority level Mid-Senior level

Employment type

• Employment type Part-time
• Industries Translation and Localization

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