Technician – Compendial Analytics
Il y a 2 jours
Thuin, Wallonia, Belgique
QUALITY ASSISTANCE S.A.
Temps plein
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Your next challenge
Ready to contribute to the quality and safety of life-changing therapies? Here's what awaits you.
As a Technician – Compendial Analytics, you will play a key role in verifying that pharmaceutical products meet the highest quality standards. Through the generation of accurate analytical data, you will directly support the development of new medicines and help accelerate access to treatments for patients worldwide.
Within our laboratory, you will contribute to essential testing activities, ensuring that every result delivered to our clients is reliable and compliant.
Your
Key Responsibilities
Here's What You'll Take Ownership Of
• Performing routine pharmacopoeia analyses in accordance with validated methods and laboratory procedures
• Conducting physicochemical testing, including osmolality, conductivity, viscosity, appearance testing and particle analysis on pharmaceutical samples
• Preparing samples, reagents and laboratory equipment required for analytical activities
• Processing analytical data and writing analysis reports
• Applying GMP requirements together with quality and safety procedures across all laboratory activities Skills you'll need to bring To Succeed In This Role, You'll Bring
• Scientific background equivalent to BAC+2 or BAC+3 or an equivalent experience
• Knowledge of pharmacopoeial testing
• Experience within a regulated environment (GMP, ISO, HACCP or similar)
• Rigour and attention to details
• English proficiency at A2 level
• Adaptability within a fast-moving analytical environment Our commitment to you Here's why you'll love working with us. Every Test You Perform Contributes To Securing The Development Of Therapies That May Improve The Lives Of Thousands Of Patients. In Return,
We Offer
• An exposure to a wide range of pharmaceutical testing activities
• An access to cutting-edge analytical technologies through continuous investment in our laboratories
• Learning and development opportunities through our Pharma Academy
• An environment that values work-life balance and employee wellbeing Who we are And why it matters We are a Belgian contract research organisation (CRO) based in Thuin, partnering with pharmaceutical companies to deliver high‑quality analytical data in line with EMA and FDA standards. With a team of nearly 280 experts and continuous investment in advanced technologies, we provide the reliable data that supports drug development and helps bring new treatments to patients faster. Here, your work contributes to a shared goal: securing every step of the process while maintaining the highest standards of quality and integrity. Joining us means becoming part of a company that values scientific rigour, collaboration, and long‑term development, both for our projects and for your career. Company Description Team up with us Quality Assistance provides the pharmaceutical industry with all the analytical services required by the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA) regulations for the development and marketing of innovative human medicinal products. We will make you a key player in our team as we seek to develop the medicines of the future and to speed up people’s access to innovative drugs.
Key Responsibilities
Here's What You'll Take Ownership Of
• Performing routine pharmacopoeia analyses in accordance with validated methods and laboratory procedures
• Conducting physicochemical testing, including osmolality, conductivity, viscosity, appearance testing and particle analysis on pharmaceutical samples
• Preparing samples, reagents and laboratory equipment required for analytical activities
• Processing analytical data and writing analysis reports
• Applying GMP requirements together with quality and safety procedures across all laboratory activities Skills you'll need to bring To Succeed In This Role, You'll Bring
• Scientific background equivalent to BAC+2 or BAC+3 or an equivalent experience
• Knowledge of pharmacopoeial testing
• Experience within a regulated environment (GMP, ISO, HACCP or similar)
• Rigour and attention to details
• English proficiency at A2 level
• Adaptability within a fast-moving analytical environment Our commitment to you Here's why you'll love working with us. Every Test You Perform Contributes To Securing The Development Of Therapies That May Improve The Lives Of Thousands Of Patients. In Return,
We Offer
• An exposure to a wide range of pharmaceutical testing activities
• An access to cutting-edge analytical technologies through continuous investment in our laboratories
• Learning and development opportunities through our Pharma Academy
• An environment that values work-life balance and employee wellbeing Who we are And why it matters We are a Belgian contract research organisation (CRO) based in Thuin, partnering with pharmaceutical companies to deliver high‑quality analytical data in line with EMA and FDA standards. With a team of nearly 280 experts and continuous investment in advanced technologies, we provide the reliable data that supports drug development and helps bring new treatments to patients faster. Here, your work contributes to a shared goal: securing every step of the process while maintaining the highest standards of quality and integrity. Joining us means becoming part of a company that values scientific rigour, collaboration, and long‑term development, both for our projects and for your career. Company Description Team up with us Quality Assistance provides the pharmaceutical industry with all the analytical services required by the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA) regulations for the development and marketing of innovative human medicinal products. We will make you a key player in our team as we seek to develop the medicines of the future and to speed up people’s access to innovative drugs.