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Hobson Prior is seeking a QA Engineer to join our client's team in supporting the quality operations of a multi-product facility. You will play a crucial role in ensuring that production activities meet high-quality standards and comply with regulations.

This is a temporary contract starting on the 12th of May until the 30th of September. Please note that applicants must have the right to live and work in Belgium and be ready to begin employment on the 12th of May.

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Responsibilities:

• Create and review quality documents related to projects.
• Monitor and assess project documents like risk assessments and validation plans.
• Provide quality guidance for both clinical and commercial manufacturing.
• Work on project documents to prevent errors and deviations.
• Ensure compliance with standard procedures and regulations.
• Offer on-site support for Good Manufacturing Practices (GMP).
• Collaborate with different departments effectively.
• Recognize when to report issues to supervisors.

Key Skills and Requirements:

• Master's degree in a scientific discipline or equivalent through experience
• Knowledge and interpretation of cGMP in a regulated environment
• Knowledge and interpretation of clinical manufacturing and regulations is an advantage
• Knowledge and experience with Quality Processes and Quality Assurance
• Excellent accuracy and attention to detail
• Independence and a strong sense of responsibility
• An enthusiastic team player and strong in communication
• Good writing skills
• Good knowledge of the English language

For more information, please contact Billy O'Brien.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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