Talent Pool - Capillary Electrophoresis

Quality Assistance; Town of Belgium (WI); Sur place; USD 48 000 - 74 000; Plein temps

Résumé du poste

Quality Assistance is expanding its analytical capabilities with a pool of Capillary Electrophoresis specialists. You will work in a hands-on lab, performing CE analyses, developing and validating methods, and contributing to regulatory submissions.

We value strong technical skills on PA800/Maurice, LC/HPLC knowledge, and experience in regulated environments. French fluency and strong scientific English writing are essential for success.

Qualifications

• Bachelor’s, Master’s or PhD in a scientific discipline.
• Strong Capillary Electrophoresis expertise on PA800 and Maurice platforms.
• Knowledge of LC/HPLC is a plus.
• Practical and theoretical understanding of analytical method transfer, development and validation.

Responsabilités

• Prepare standard solutions required for analysis.
• Perform analytical testing using Capillary Electrophoresis.
• Execute routine analyses based on established methods and protocols.
• Transfer, develop or validate analytical methods according to project needs.
• Review raw data in line with quality requirements.
• Interpret results and write analytical reports and documentation.
• Manage stability studies.

Connaissances

Capillary Electrophoresis on PA800

Maurice platforms

LC/ UHPLC knowledge

Analytical method transfer

Method validation

Empower software

regulated environment

Scientific writing in English

French language fluency

Formation

Bachelor’s/Master’s/PhD in a relevant science

Outils

Empower

Description du poste

As our analytical activities continue to expand, we are building a talent pool of Capillary Electrophoresis specialists to support future opportunities within our laboratories.

Capillary Electrophoresis provides critical information on the quality, consistency and stability of biopharmaceutical products throughout their development. By generating reliable analytical data, you'll contribute to the scientific evidence that supports regulatory submissions and informs important project decisions.

Working in a hands-on laboratory environment, you'll spend more than 60% of your time at the bench, applying your expertise to generate accurate results, investigate analytical questions and support pharmaceutical projects from development through to regulatory submission. Ultimately, the quality of your work helps bring safe and effective treatments closer to the patients who need them.

• Prepare standard solutions required for analysis
• Perform analytical testing using Capillary Electrophoresis
• Execute routine analyses based on established methods and protocols
• Transfer, develop or validate analytical methods according to project needs
• Review raw data in line with quality requirements
• Interpret results and write analytical reports and associated scientific documentation
• Manage stability studies

Skills you'll need to bring

To succeed in this role, you'll bring:

• Scientific degree - Bachelor’s, Master’s or PhD level
• Strong technical expertise in Capillary Electrophoresis on PA800, Maurice platforms
• Knowledge of liquid chromatography HPLC / (U)HPLC is a plus
• Practical and theoretical understanding of analytical methods including transfer, development and validation
• Experience with software such as Empower
• Working experience in a regulated environment
• Fluency in French and good scientific writing skills in English

From day one, you'll have access to a structured onboarding programme and continuous learning opportunities designed to strengthen your technical expertise in analytical sciences.

You'll also benefit from:

• State-of-the-art equipment that keeps us at the forefront of the industry
• A collaborative scientific culture where knowledge sharing is encouraged
• A working environment that supports wellbeing, flexibility and career growth
• The satisfaction of contributing to medicines that can make a meaningful difference to patients worldwide

Who we are

And why it matters

At Quality Assistance, analytical science supports one clear objective: helping innovative treatments reach patients faster.

From our site in Thuin, we work alongside pharmaceutical companies, providing analytical data that meets the expectations of international regulatory authorities, including the EMA and FDA. Supported by a team of nearly 280 experts and continuous investment in advanced technologies, we help our partners move their projects forward through reliable, high-quality data. Every analysis contributes to maintaining the safety, quality and integrity required throughout the drug development process.

Joining us means becoming part of a collaborative environment where scientific expertise is valued, professional growth is encouraged, and every contribution helps advance public health.