Duration: 6 months with possibility of extension About us
Adryan is an internationally operating services group with offices in The Netherlands and Switzerland. We specialize in providing a full range of services for the life sciences industry, focusing on Project Management, Technical Operations, CQV, and Compliance. Our teams work with top clients in the life sciences sector, ensuring the highest quality and commitment. QC Analyst
Responsibilities
Develop, optimize, qualify, and validate existing and new analytical methods for pharmaceutical raw materials, excipients, active pharmaceutical ingredients (APIs), and intermediates in compliance with cGMP requirements. Independently perform analytical testing to support pharmaceutical development and manufacturing activities. Assist in the preparation of GMP-related documentation, including analytical test methods, validation protocols and reports, laboratory procedures, and standard operating procedures (SOPs). Conduct troubleshooting activities and investigate analytical deviations, out-of-specification (OOS), and other laboratory investigations. Profile / Qualifications
Completed vocational training as a Chemical Laboratory Technician (or equivalent qualification). Minimum of 2 years of professional experience in analytical development or instrumental analysis. Experience working in a cGMP-regulated pharmaceutical environment. Hands‑on experience with common analytical techniques, with a strong focus on HPLC and GC. Reliable, team‑oriented, and resilient, with the ability to work independently in a structured and organized manner. Good command of German and technical English, both written and spoken. Proficient in standard computer applications (MS Office and laboratory software).
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Adryan is an internationally operating services group with offices in The Netherlands and Switzerland. We specialize in providing a full range of services for the life sciences industry, focusing on Project Management, Technical Operations, CQV, and Compliance. Our teams work with top clients in the life sciences sector, ensuring the highest quality and commitment. QC Analyst
Responsibilities
Develop, optimize, qualify, and validate existing and new analytical methods for pharmaceutical raw materials, excipients, active pharmaceutical ingredients (APIs), and intermediates in compliance with cGMP requirements. Independently perform analytical testing to support pharmaceutical development and manufacturing activities. Assist in the preparation of GMP-related documentation, including analytical test methods, validation protocols and reports, laboratory procedures, and standard operating procedures (SOPs). Conduct troubleshooting activities and investigate analytical deviations, out-of-specification (OOS), and other laboratory investigations. Profile / Qualifications
Completed vocational training as a Chemical Laboratory Technician (or equivalent qualification). Minimum of 2 years of professional experience in analytical development or instrumental analysis. Experience working in a cGMP-regulated pharmaceutical environment. Hands‑on experience with common analytical techniques, with a strong focus on HPLC and GC. Reliable, team‑oriented, and resilient, with the ability to work independently in a structured and organized manner. Good command of German and technical English, both written and spoken. Proficient in standard computer applications (MS Office and laboratory software).
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Quality Control Analyst Arbeitgeber: Adryan
Adryan bietet eine hervorragende Arbeitsumgebung in Basel, wo Teamarbeit und Innovation im Mittelpunkt stehen. Unsere Mitarbeiter profitieren von flexiblen Arbeitszeiten, kontinuierlichen Weiterbildungsmöglichkeiten und einem unterstützenden Arbeitsklima, das persönliches Wachstum fördert. Zudem ermöglicht die Lage in Basel den Zugang zu einem dynamischen Netzwerk in der Pharmaindustrie, was zusätzliche Karrierechancen eröffnet.
