Quality Internship

Job description

<p><strong><span>Quality Internship</span></strong></p><p> </p><p><strong><u>COMPANY BACKGROUND / CULTURE</u></strong></p><p>Nuritas’ mission is to improve the lives of billions, and our vision is to provide the hero ingredient in everyday products.

We are transforming the discovery of bioactive ingredients using AI, deep learning, and genomics to unlock peptides from natural sources like plants and food.</p><p> </p><p>Our proprietary platform, Magnifier, uses advanced machine learning and our extensive dataset of molecules to identify natural peptides with specific health benefits.

We optimize these molecules for stability and scalability, ensuring they perform in real-world applications.

Our plant peptide ingredients include PeptiStrong® for protein amplification and muscle health, and PeptiSleepTM for improving deep and REM sleep.

Through our ingredients, customers can create better products that are truly differentiated in addressing consumer needs.</p><p> </p><p>Founded in 2014 by Dr. Nora Khaldi, the company has built the world’s largest peptide knowledge base and formed high-profile partnerships with companies like Nestle, Mars, and Sumitomo Corporation.

Its team, diverse in nationality and gender, is driven by innovation and passion to bring nature’s benefits to the world.</p><p> </p><p> </p><p><strong><span>The Position:</span></strong> <br>Based in Dublin, the <strong>Quality Intern</strong> will play a key role in supporting our commitment to excellence.

Reporting directly to the Quality System Lead, this internship offers hands-on experience in maintaining and improving our quality management systems, exposure to industry best practices, and the opportunity to contribute to meaningful projects that make a real impact.

This role is ideal for a motivated student eager to gain practical experience in a fast-paced, innovative environment while learning from experienced quality professionals.</p><p> <br><strong><span>Main role may include (not limited to):</span></strong> </p><p><span>·</span><span style="font-family: Times New Roman">       </span>Review and verify the accuracy and completeness of Certificate of Analysis (COAs) and Material Safety Data Sheets (MSDSs) for raw materials and finished products.</p><p><span>·</span><span style="font-family: Times New Roman">       </span>Identify inconsistencies or gaps in documentation and communicate findings to the quality team.</p><p><span>·</span><span style="font-family: Times New Roman">       </span>Assist in the establishment of new processes and acceptance criteria.</p><p><span>·</span><span style="font-family: Times New Roman">       </span>Assist in the development, organization and updating of standard operating procedures (SOPs), work instructions and other controlled documents.</p><p><span>·</span><span style="font-family: Times New Roman">       </span>Support the implementation and maintenance of the Quality Management System (QMS), including document control and process mapping.</p><p><span>·</span><span style="font-family: Times New Roman">       </span>Help prepare documentation</p><p> </p><p><strong><span>Basic Requirements</span></strong></p><p><span>·</span><span style="font-family: Times New Roman">       </span> Currently pursing or recently completed a degree in Life Sciences, Quality Assurance, Regulatory Affairs, Pharmaceutical Science or related field.</p><p><span>·</span><span style="font-family: Times New Roman">       </span>Strong attention to detail and the ability to follow structures review process</p><p><span>·</span><span style="font-family: Times New Roman">       </span>Excellent written and verbal communication skills.</p><p> </p><p><strong><span>Preferred requirements</span></strong></p><p><span>·</span><span style="font-family: Times New Roman">       </span>Familiarity with quality systems or regulatory documentation is an advantage.</p><p><span>·</span><span style="font-family: Times New Roman">       </span><span>Proficiency in Microsoft Office (Word, Excel, Outlook), and experience with document management systems is a plus.</span></p><p><span>·</span><span style="font-family: Times New Roman">       </span><span>Self-motivated with strong organizational skills</span></p><p><span>·</span><span style="font-family: Times New Roman">       </span>Micro and laboratory experience</p><p> </p><p><span>What you’ll gain</span></p><p><span>·</span><span style="font-family: Times New Roman">       </span><span>Real world experience in quality assurance within a regulated industry.</span></p><p><span>·</span><span style="font-family: Times New Roman">       </span><span>Exposure to regulatory documentation, compliance and QMS implementation.</span></p><p><span>·</span><span style="font-family: Times New Roman">       </span><span>Mentorship from experienced quality professionals.</span></p><p><span>·</span><span style="font-family: Times New Roman">       </span><span>Opportunity to contribute to meaningful improvements in product safety and quality.</span></p>

Required Skill Profession

Business Operations Specialists