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Our client is seeking a Qualification-Validation Engineer to join a prominent company in the pharmaceutical industry based in Belgium. As a Qualification-Validation Engineer, you will play a crucial role in ensuring the quality and compliance of the site’s systems and processes.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualification-Validation Engineer will be varied however the key duties and responsibilities are as follows:
1. Define and monitor qualification/validation strategies in compliance with Good Manufacturing Practices and safety regulations, adhering to the project’s Validation Master Plan.
2. Develop and validate cleaning processes for equipment, ensuring compliance with site-specific Validation Master Plans and safety regulations.
3. Execute and verify qualification/validation tests for installations, involving future users and following current procedures.
4. Plan, organise, and coordinate validation activities in collaboration with the project team.
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:
1. Relevant degree in a scientific field.
2. Proven industry experience in validation.
3. A working knowledge and practical experience with pharmaceutical industrial processes and IT/Computer System Validation.
Key Words:
Qualification Engineer / Validation Engineer / Pharmaceutical Validation / GMP / Cleaning Validation / Process Validation / CSV / Braine-l'Alleud / Belgium / Pharmaceutical Industry / Project Coordination / Quality Assurance
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Our client is seeking a Qualification-Validation Engineer to join a prominent company in the pharmaceutical industry based in Belgium. As a Qualification-Validation Engineer, you will play a crucial role in ensuring the quality and compliance of the site’s systems and processes.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualification-Validation Engineer will be varied however the key duties and responsibilities are as follows:
1. Define and monitor qualification/validation strategies in compliance with Good Manufacturing Practices and safety regulations, adhering to the project’s Validation Master Plan.
2. Develop and validate cleaning processes for equipment, ensuring compliance with site-specific Validation Master Plans and safety regulations.
3. Execute and verify qualification/validation tests for installations, involving future users and following current procedures.
4. Plan, organise, and coordinate validation activities in collaboration with the project team.
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:
1. Relevant degree in a scientific field.
2. Proven industry experience in validation.
3. A working knowledge and practical experience with pharmaceutical industrial processes and IT/Computer System Validation.
Key Words:
Qualification Engineer / Validation Engineer / Pharmaceutical Validation / GMP / Cleaning Validation / Process Validation / CSV / Braine-l'Alleud / Belgium / Pharmaceutical Industry / Project Coordination / Quality Assurance
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
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