Technician – Compendial Analytics

Quality Assistance Ltd.; Henegouwen; On-site; EUR 28,000 - 36,000; Full time

Benefits offered by this job

Pharma Academy

Work‑life balance

Career development

Cutting-edge tech

Job summary

Quality Assistance Ltd. is seeking a Technician – Compendial Analytics to verify that pharmaceutical products meet high quality standards. You will generate accurate analytical data to support development of medicines and accelerate patient access to treatments worldwide.

Within our laboratory, you will contribute to essential testing activities, ensuring every result is reliable and compliant. You will work under GMP and ISO/HACCP guidelines in a fast-moving environment.

Qualifications

• BAC+2/BAC+3 or equivalent experience.
• Knowledge of pharmacopoeial testing.
• Experience in regulated environments (GMP, ISO, HACCP or similar).
• Rigour and attention to detail.
• English proficiency at A2 level.
• Adaptability in a fast-moving analytical environment.

Responsibilities

• 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

GMP/ISO awareness

Attention to detail

Analytical testing

Adaptability

English A2

Education

BAC+2 or BAC+3

Job description

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.

• 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

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.