Offre spontanée – Soins
Veröffentlicht:
01 April 2024Pensum:
100%Vertrag:
Festanstellung- Arbeitsort:Vevey
<div class="basic-layout__main"><div class="block__title hidden--from-l">job details</div><div class="body-copy hidden--from-l"><p> </p><p>An exciting new opportunity has arisen to join us as Quality Assurance Qualification & Validation Engineer for our Biotech drug substance plant in Corsier-sur-Vevey.<br/>As an integral member of the Quality Unit, you provide QA expertise for Process Validation and Analytical Validation:</p><p> </p><ul><li>You elaborate the qualification/validation strategies, review and approval of protocols and reports, participates to risk analysis, identifies gap and purposes remediation plan</li><li>You act as Quality Subject Matter Expert on specific topics and participate in risk assessments and handle deviations on these topics </li><li>You review and/or approve qualification/validation documents, risk assessment, SOPs and take quality decisions according to company standards</li></ul><p> </p><p>The activities of the QA Expert cover all qualification/validation phases from Basic Design until 1st use of equipment/raw material.10. You ensure GMP compliance during all phases of qualification/validation.</p><p> </p></div><ul class="link-list link-list--single accordion no-overflow-anchor" id="jd-accordion"><li class="link-list__item"><div aria-label="" class="collapsible__trigger" data-rs-collapsible="filter" data-rs-toggable="true" role="button" tabindex="0"><h3 class="link-list__link">qualifications</h3><span class="hidden--from-l toggle-arrow icon"><svg><use xlink:href="/themes/custom/bluex/dist/assets/image/icons.svg#chevron-down"></use></svg></span><span class="hidden--until-l toggle-arrow icon icon--l"><svg><use xlink:href="/themes/custom/bluex/dist/assets/image/icons.svg#chevron-down-30"></use></svg></span></div><div class="body-copy collapsible__content rich-text" data-rs-collapsible-content=""><div class="collapsible__content--wrapper"><ul><li>You have a university degree with at least 5 years of experience in pharmaceutical quality environment </li><li>Proven experience in analytical methods validation and manufacturing process validation </li><li>Strong communication and strong team spirit</li><li>Good stress resistance</li><li>Fluent in French and English (oral & written)</li></ul></div></div></li></ul></div><div class="person__info"><h3 class="person__name text-transform--none">Andreia Lourenço</h3><ul class="contact-details"><li class="contact-details__item"><span class="contact-details__link"><span class="icon fill-brand--dark-blue icon--inline"></span><span>Randstad Merck Aubonne</span></span></li></ul></div>
Kontakt
Ensemble hospitalier de la Côte