Qualification Validation Engineer

Il y a 2 jours

Wallonië, Belgique Hyper Recruitment Solutions Ltd Temps plein 60 000 € - 80 000 €/an

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.

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.