Quality Control Laboratory Analyst – Pharmaceutical Industry

Quality Control Laboratory Analyst – Pharmaceutical Industry

Wallonia, Belgium (On-site)

About Nalys

Nalys is a fast-growing consultancy company specialized in high-tech engineering and life sciences. Founded 15 years ago, we partner with leading organizations to deliver innovative solutions and expert support across a wide range of technical domains. At Nalys, we believe in combining deep expertise with a human-centric approach, empowering our consultants to thrive and our clients to succeed.

Joining Nalys means becoming part of a collaborative, agile, and forward-thinking team that values excellence, innovation, and continuous growth.

Job Description

As a Quality Control Laboratory Analyst, you will join the QC department of a major pharmaceutical organization, within a large, structured team dedicated to analytical testing. The assignment starts as soon as possible and runs until the end of the year, with a possible extension based on performance.

The Role & Responsibilities

• Perform analytical testing on pharmaceutical products (intermediates, APIs, bulk and finished products) following established procedures
• Prepare samples, reagents, and analytical equipment (HPLC, GC)
• Launch, monitor, and process analytical runs
• Review analytical data and ensure compliance with specifications
• Contribute to deviation investigations and corrective actions
• Ensure accurate documentation of lab activities (raw data recording)
• Participate in lab maintenance, calibration follow-up, and housekeeping
• Organize your work autonomously based on weekly planning
• Join daily or regular team follow-up meetings.

Skills & Qualifications

• You hold a Bachelor's degree in a scientific field (minimum requirement)
• You have around 5 years of relevant experience for a medior profile (more junior profiles considered if strong HPLC skills)
• You have solid, hands-on experience with HPLC (critical requirement) and physico-chemical laboratory analysis
• You have a strong command of Empower software
• You understand GMP requirements and quality standards (e.g. ALCOA+)
• You are autonomous, proactive, and comfortable working in a large team
• You are fluent in French, with good reading comprehension of technical English
• A plus: experience with GC and/or NMR, familiarity with LIMS, TopSpin, or similar lab systems.

Your Team

You will join a large Quality Control organization of around 50 people, structured into 5 teams of 8 to 10 members each, covering bench work, data review, and deviation/documentation management. You may be assigned across different teams depending on workload and training progress.

What We Offer

• A human‐scaled consulting company focused on expertise, partnership, and career development
• Long‐term assignments with leading pharmaceutical players
• Continuous learning through technical coaching, training, and knowledge sharing
• A supportive culture that values autonomy, trust, and impact.

The Recruitment Process

By applying for the \"Project Scheduler\" position, you will go through the following steps in our recruitment process:

• Olivia Braszko, TA Specialist, will analyze your resume and schedule a first screening.
• You will have a second interview with one of our technical experts
• The last interview will be with our Business Unit Director, Jimmy Rousseaux.

Interested? xlxgzvr

Apply directly via this post and let's discuss your motivation through a first teams meeting