Qualification Validation Engineer

Hyper Recruitment Solutions; Wallonië; Sur place; EUR 55 000 - 75 000; Plein temps

Résumé du poste

Hyper Recruitment Solutions is seeking a Qualifications Validation Engineer for a leading pharmaceutical company in the Walloon region of Belgium. The role focuses on ensuring qualification of production systems in line with GMP, HSE and site Validation Master Plans.

You will oversee qualification activities for GMP utilities, validate production and cleaning processes, and maintain quality systems to support audits and compliance.

Qualifications

• Degree in a scientific or engineering discipline.
• Experience in pharmaceutical production or validation.
• Knowledge of GMP regulations and validation processes.

Responsabilités

• Qualify computerized and non-computerized production systems per Validation Master Plan.
• Oversee GMP utilities qualification in line with site plans.
• Validate production and cleaning processes and support audits.
• Maintain quality systems for qualification and validation activities.

Connaissances

GMP knowledge

Validation

HVAC qualification

IT validation

Bilingual FR/EN

Analytical skills

Formation

Bachelor's degree in a scientific or engineering discipline

Description du poste

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:

• 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:

• - 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.