Validation Engineer

Hyper Recruitment Solutions; Wallonië; Sur place; EUR 45 000 - 75 000; Plein temps

Résumé du poste

Hyper Recruitment Solutions is supporting a leading pharmaceutical organisation in Belgium's Walloon region to recruit a Validation Engineer. You will qualify production systems and equipment, ensuring compliance with GMP, safety guidelines, and site Validation Master Plans.

You will contribute to qualification of both computerised and non-computerised systems, manage validation activities for GMP utilities, and drive audits readiness.

Qualifications

• Proven experience in pharmaceutical validation and qualification.
• Working knowledge of GMP regulations.
• Familiarity with validation master plans and HSE guidelines.

Responsabilités

• Qualify computerised and non-computerised production or development systems.
• Oversee GMP utilities qualification and process validation.
• Maintain quality systems for qualification activities and audits.
• Develop operational qualification activities for production equipment.

Connaissances

Pharmaceutical validation

GMP knowledge

HSE guidelines

Formation

Degree in science or engineering

Description du poste

A leading organisation in the pharmaceutical industry is seeking a Validation Engineer to join their team in the Walloon region, Belgium. As a Validation Engineer, you will play a crucial role in ensuring the qualification and validation of production systems and equipment, adhering to applicable regulations and safety guidelines.

Key Duties and Responsibilities

• You will ensure the qualification of computerised and non-computerised production or development systems in compliance with applicable regulations and site Validation Master Plans.
• You will oversee the qualification activities of GMP utilities and the validation of processes, ensuring adherence to GMP, HSE rules, and the site Validation Master Plan.
• You will maintain the quality systems governing qualification and validation activities, ensuring compliance and audit readiness.
• You will develop and implement operational qualification activities for production systems and equipment, ensuring their qualified status according to initial and periodic review schedules.

Role Requirements

• Relevant degree in a scientific or engineering discipline.
• Proven industry experience in pharmaceutical validation and qualification.
• A working knowledge and practical experience with GMP regulations, validation master plans, and HSE guidelines.

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements.