Laboratory Analysis II (Analyst HPLC/UPLC)
Location – Antwerp
Job content:
- Perform a wide range of laboratory analyses within a pharmaceutical manufacturing environment.
- Ensure accuracy and compliance with applicable standards, procedures, and work instructions.
- Carry out routine and specialized tests (HPLC, UPLC, CGE, ELISA, particle analysis).
- Work in accordance with Standard Operating Procedures (SOPs).
- Support process development and root cause investigations according to established protocols.
- Maintain the laboratory environment and ensure compliance with safety regulations.
- Manage the maintenance and calibration of laboratory equipment required for process development.
- Depending on the assignment, tasks may also include support with analytical method validation, management and processing of samples, inventory control of reagents and consumables, participation in improvement projects, and execution of administrative tasks.
- Ensure that laboratory Key Performance Indicators (KPIs) are achieved.
Profile:
- Bachelor’s or master’s degree in Life Sciences, or equivalent through experience.
- Good command of Dutch and English.
- Strong analytical skills, attention to detail, and a results-oriented mindset.
- Ability to follow written and verbal instructions accurately, with strict adherence to safety procedures and GLP guidelines.
- Proficiency in laboratory information management systems (LIMS), MS Office, and other relevant PC software.
- Strong problem-solving skills, with the ability to investigate the root causes of issues and deviations and develop appropriate solutions.
- Excellent interpersonal and communication skills for smooth collaboration with internal teams and external stakeholders.
- Experience as a laboratory analyst in the biochemical or medical sector, or within Quality Control, is an advantage.
- Experience with at least one of the following techniques is required: UPLC/HPLC (preferably on the Empower platform), capillary gel electrophoresis, or ELISA.
- Flexibility in working hours is required; for senior profiles, experience in coaching junior colleagues and in method validation or instrument implementation is an asset.
What can you expect?
You will join an international and innovative working environment where safety, quality, and collaboration are central. You will receive a competitive salary package and extensive fringe benefits, along with plenty of opportunities to further develop your technical knowledge and contribute to challenging projects.