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Lead QC Chemist – Chromatography Method Dev & Validation
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- Ireland
- Ireland
Über
Below covers everything you need to know about what this opportunity entails, as well as what is expected from applicants.
This role requires expertise in chromatographic method development and validation, ensuring compliance with GMP regulations.
Candidates should have 4+ years of experience in a pharmaceutical QC environment and proven leadership in analytical activities.
We offer competitive salary packages, benefits including performance-related bonuses, medical insurance, and support for career development. xcfaprz
Flexitime working arrangements are available in Loughbeg, Ireland.
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Sprachkenntnisse
- English
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