Qualification Validation Engineer

Hyper Recruitment Solutions; Waals-Brabant; On-site; EUR 60,000 - 90,000; Full time

Job summary

Hyper Recruitment Solutions Ltd in Belgium is seeking a Qualification Validation Engineer to qualify production and development systems in line with GMP, CFR, and ICH standards. You will contribute to maintaining robust quality systems and collaborate with internal teams and external partners.

The role requires at least 3 years of pharmaceutical validation experience, including packaging qualification/validation, plus strong analytical skills and ability to work with diverse stakeholders.

Qualifications

• Relevant 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

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

Skills

GMP CFR ICH knowledge

Bilingual French & English

Analytical skills

Stakeholder management

Quality mindset

Education

Bachelor's degree in science or 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

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

• 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.
• As the Qualification Validation Engineer, you will oversee the qualification activities of GMP utilities, ensuring adherence to GMP and HSE rules.
• As the Qualification Validation Engineer, you will validate processes and cleaning procedures of equipment involved in manufacturing processes.
• As the Qualification Validation Engineer, you will maintain the quality systems supporting qualification and validation activities.

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:

• Relevant degree in a scientific or engineering discipline.
• Proven industry experience in pharmaceutical validation, ideally 3 years minimum within Packaging qualification and validation.
• 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. Don't miss out on this chance to advance your career in the pharmaceutical industry.

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

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