Quality Control Laboratory Analyst – Pharmaceutical Industry

Quality Control Laboratory Analyst – Pharmaceutical Industry

Is your CV ready If so, and you are confident this is the role for you, make sure to apply asap.

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:

1. Olivia Braszko, TA Specialist, will analyze your resume and schedule a first screening.
2. You will have a second interview with one of our technical experts
3. 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