Qualification Validation Engineer

Hyper Recruitment Solutions; Wallonië; On-site; EUR 55,000 - 75,000; Full time

Job summary

Hyper Recruitment Solutions is seeking a Qualification Validation Engineer in the Walloon region of Belgium. You will ensure qualification of production and development systems in alignment with regulatory requirements and site validation master plans, while adhering to GMP, CFR, ICH and HSE standards.

The role requires a scientific or engineering degree and 3+ years in pharmaceutical validation, with strong GMP knowledge and ability to manage interactions with external suppliers and internal

Qualifications

• Degree in a scientific or engineering discipline.
• 3+ years in pharmaceutical validation, ideally packaging qualification/validation.
• Working knowledge of GMP regulations and validation processes.

Responsibilities

• Qualify production and development systems in line with regulations and Validation Master Plans.
• Oversee GMP utilities qualification activities per GMP/HSE rules.
• Validate processes and cleaning procedures for manufacturing equipment.
• Maintain quality systems supporting qualification and validation activities.

Skills

French/English proficiency

Analytical/problem-solving

GMP/CFR/ICH/HSE knowledge

Qualification of production systems

Education

Degree in science/engineering

Job description

Are you ready to take your career to the next level in the pharmaceutical industry? A leading company in the Walloon region, Belgium is seeking a dedicated and skilled Qualification Validation Engineer. This role offers the chance to be at the forefront of ensuring the highest standards of production and development systems, both computerised and non-computerised, in compliance with applicable regulations and safety rules.

KEY DUTIES AND RESPONSIBILITIES:

• 1. As the Qualification Validation Engineer, you will ensure the qualification of production and development systems in compliance with applicable regulations and site Validation Master Plans.
• 2. As the Qualification Validation Engineer, you will oversee the qualification activities of GMP utilities, ensuring adherence to GMP and HSE rules.
• 3. As the Qualification Validation Engineer, you will validate processes and cleaning procedures of equipment involved in manufacturing processes.
• 4. As the Qualification Validation Engineer, you will maintain the quality systems supporting qualification and validation activities.

ROLE REQUIREMENTS:

• 1. Relevant degree in a scientific or engineering discipline.
• 2. Proven industry experience in pharmaceutical validation, ideally 3 years minimum within Packaging qualification and validation.
• 3. A working knowledge and practical experience with GMP regulations and validation processes.

Skills and Experience:

• - Experience with qualification of production systems and equipment.
• - Knowledge of GMP, CFR, ICH, and HSE standards.
• - Proficiency in both French and English.
• - Strong analytical and problem-solving skills.
• - Ability to manage interactions with external suppliers and internal stakeholders.

This role is perfect for someone who thrives in a dynamic environment and is passionate about maintaining high standards in pharmaceutical production. If you are looking to make a significant impact and grow within a supportive and innovative team, this is the role for you.

Key Words:

Pharma Validation / GMP / Pharmaceutical / Validation Associate / Production Systems / Compliance / Quality Systems / HSE / Braine-l'Alleud / Qualification / Regulatory Standards