Key Skills

Job Description

About the role Do you enjoy hands-on laboratory work and applying a variety of analytical techniques in a pharmaceutical environment? Join our Quality Control team as a QC Analyst and help ensure the quality of our materials and products. While your work includes routine laboratory analyses, your activities will vary as you are involved in different stages of the QC process. You will independently perform analyses, accurately review and document results, and ensure compliance with applicable quality requirements. This variety makes the role both diverse and dynamic, requiring a flexible mindset, adaptability and a willingness to switch between different tasks and priorities. What will you do Perform immunochemical analyses such as ELISA, SDS-PAGE, Western Blot and ImmunoCAP. Perform spectrophotometric analyses, including protein determination using the Bradford assay, phenol and supernatant measurements. Perform physicochemical tests such as pH, osmolality and visual quality inspections. Work with chromatographic techniques such as ultra-performance liquid chromatography (UPLC), using size-exclusion chromatography (SEC). Ensure accurate documentation, review and reporting of analytical results in compliance with GMP/GcLP guidelines and internal procedures. Support daily laboratory activities, including inventory, equipment status tracking, logbooks and documentation. Report deviations and contribute to investigations, change controls, OOS actions, CAPAs and continuous improvements. Participate in equipment and system validation, support improvements to analytical methods and help maintain or update SOPs. Share knowledge and provide training to colleagues where needed. Your profile An MLO-level education in biochemistry, biotechnology, life sciences or a related laboratory discipline. Practical experience in a biochemical laboratory is an advantage; familiarity with the listed techniques is welcome. Knowledge of GMP requirements and laboratory safety; experience with GcLP is an advantage. Good spoken and written communication skills in Dutch and English. Familiarity with the pharmaceutical industry, MS Office and LIMS. An accurate, analytical and quality-focused approach, combined with a sense of responsibility, teamwork and willingness to learn. We offer: Competitive salary, including 13th months and annual reward scheme 25 vacation days (based on a fulltime agreement) 5 additional vacation days NS business card or; Travel allowance by car or bike

Core Responsibilities

Perform and document a range of biochemical, immunochemical, spectrophotometric, physicochemical, and chromatographic analyses while ensuring compliance with GMP/GcLP requirements. Support laboratory operations, investigations, validation, method and SOP improvements, and colleague training.

Requirements

An MLO-level qualification in biochemistry, biotechnology, life sciences, or a related laboratory discipline is required; practical biochemical laboratory experience and familiarity with the listed techniques are advantageous. The role calls for knowledge of GMP and laboratory safety, good Dutch and English communication skills, familiarity with the pharmaceutical industry, MS Office and LIMS, and an accurate, analytical, quality-focused, collaborative approach.

Benefits

• 13th-Month Salary
• Annual Reward Scheme
• 25 Vacation Days
• 5 Additional Vacation Days
• Public Transport Business Card
• Travel Allowance