Qualification Validation Engineer
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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.