Job Description
As part of The Adecco Group, Akkodis has extensive industrial experience and deep expertise in key technology areas. By combining IT and engineering expertise, we offer a unique end-to-end solution through our four service areas – Consulting, Solutions, Talents, and Academy – to help our clients rethink product development and business processes, increase productivity, reduce time to market, and shape a smarter, more sustainable future.About the RoleWe are seeking a Quality Control (QC) Specialist with expertise in material analysis to join our team in Geneva. In this role, you will ensure that raw materials, intermediates, and final products consistently meet regulatory safety and quality standards. You will play a key role in analytical testing, compliance, and cross-functional collaboration, supporting our commitment to product excellence.ResponsibilitiesPerform analytical characterization of raw materials, intermediates, and finished products.Conduct QC tests including purity checks, instrumental analysis, and other analytical techniques.Ensure accuracy and completeness of documentation in line with GMP and regulatory requirements.Manage and investigate deviations, OOS (Out-of-Specification) results, and non-conformities.Support and execute analytical method transfers between internal laboratories and external partners.Provide technical expertise during method validation, verification, and troubleshooting to guarantee reliable implementation across sites.Collaborate cross-functionally with R&D, production, and regulatory teams to resolve issues and align on quality standards.Support regulatory audits and maintain up-to-date knowledge of relevant quality and compliance regulations.Contribute to the continuous improvement of QC processes and analytical methodologies.Qualifications & BackgroundDegree in Chemistry, Materials Science, Chemical Engineering or related field.Professional experience in Quality Control within chemical, pharmaceutical, or cosmetics industries.Solid knowledge of analytical methods and laboratory techniques (e.g. HPLC, GC, spectroscopy, instrumental analysis).Familiarity with GMP, ISO standards, and regulatory frameworks.Strong problem-solving skills, attention to detail, and ability to manage documentation and compliance tasks.Fluent in French (good level of English is a plus)
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