Pauwels Consulting

Our client, a leading pharmaceutical company, is looking for a Qualification &amp; Validation specialist to strengthen their manufacturing team. The role focuses on supporting a periodic qualification review project and various packaging-related equipment projects within a production environment.
Responsibilities
<ul>
<li>Support the periodic review of qualification status for production and assembly systems.</li>
<li>Execute qualification and validation activities for production and packaging equipment.</li>
<li>Manage assembly and packaging validation tasks for combination products.</li>
<li>Identify technical issues and propose appropriate solutions during the validation lifecycle.</li>
<li>Prepare and execute qualification and validation protocols while maintaining technical documentation.</li>
<li>Investigate deviations and technical issues related to equipment qualification.</li>
<li>Collaborate with stakeholders to ensure timely execution and follow-up of assigned activities.</li>
</ul>
Requirements
<ul>
<li>You have 3+ years of experience in Qualification &amp; Validation within a pharmaceutical manufacturing environment.</li>
<li>You bring hands-on expertise in the qualification of production and packaging equipment, specifically for combination products.</li>
<li>You possess strong problem-solving skills and a proactive, autonomous mindset.</li>
<li>You are fluent in French with technical reading and writing proficiency in English.</li>
</ul>
Nice to Haves
<ul>
<li>Experience in Computerized System Validation (CSV).</li>
<li>Additional experience within a regulated pharmaceutical environment.</li>
</ul>

Qualification & Validation Engineer - Packaging & Production

Qualification & Validation Engineer - Packaging & Production

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