A leading company in the pharmaceutical industry is seeking a Qualification Validation Engineer to join their team in the Walloon region, Belgium. As a Qualification Validation Engineer, you will play a crucial role in maintaining and enhancing the quality and compliance of production systems and processes.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Qualification Validation Engineer will be varied however the key duties and responsibilities are as follows:

1. As the Qualification Validation Engineer, you will ensure the qualification of both computerized and non-computerized production systems in compliance with applicable regulations and site-specific Validation Master Plans.

2. As the Qualification Validation Engineer, you will oversee the qualification activities for GMP utilities, ensuring adherence to GMP and HSE rules, and alignment with the site's Validation Master Plan.

3. As the Qualification Validation Engineer, you will validate production and cleaning processes, maintaining compliance with GMP, HSE rules, and the site's Validation Master Plan.

4. As the Qualification Validation Engineer, you will maintain the quality systems governing qualification and validation activities, ensuring continuous compliance and readiness for audits.

ROLE REQUIREMENTS:





To be successful in your application to this exciting role as the Qualification Validation Engineer we are looking to identify the following on your profile and past history:

1. Relevant degree in a scientific or engineering discipline.

2. Proven industry experience in pharmaceutical production or validation.

3. A working knowledge and practical experience with GMP regulations and validation processes.

Skills and Experience:

- Expertise in production techniques (chemical/pharmaceutical/packaging).

- Knowledge of utility and HVAC qualification.

- Familiarity with IT/Computer System Validation.

- Understanding of GMP, CFR, ICH, and HSE standards.

- Strong analytical and problem-solving skills.

- Proficiency in French and English.

Key Words:

Qualification / Validation / pharmaceutical production / GMP / validation processes / quality systems / compliance / HSE standards / utility qualification / HVAC / IT validation

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.

📌 Qualification validation engineer (España)
🏢 Hyper Recruitment Solutions
📍 España