Quality Control Laboratory Analyst – Pharmaceutical Industry

Nalys; Wallonië; Sur place; EUR 55 000 - 70 000; Plein temps

Avantages offerts par ce poste

Long-term assignments

Technical coaching

Autonomy & trust culture

Résumé du poste

Nalys is seeking a Quality Control Laboratory Analyst to join a major pharmaceutical organization in Wallonia, Belgium. You will be part of a large QC team focused on analytical testing, data review, and deviation management, with an end-of-year assignment and potential extension based on performance.

You will work in a structured, collaborative environment of about 50 QC colleagues across multiple sub-teams, contributing to documentation, calibration, and continuous improvement using HPLC and

Qualifications

• Bachelor's degree in a scientific field (minimum requirement).
• Around 5 years of relevant medior experience; strong HPLC skills may compensate.
• Solid hands-on experience with HPLC and physico-chemical analysis.
• Fluent in French with reading proficiency in technical English.

Responsabilités

• Perform analytical testing on pharmaceutical products following established procedures (intermediates, APIs, bulk, finished products).
• Prepare samples, reagents, and analytical equipment (HPLC, GC).
• Review analytical data and ensure compliance with specifications; contribute to deviation investigations and corrective actions.
• Ensure accurate documentation of lab activities (raw data recording) and participate in calibration follow-up.
• Organize work autonomously based on weekly planning and join regular team meetings.

Connaissances

HPLC

Empower software

GMP/ALCOA+

Autonomous / proactive

French language

Formation

Bachelor's degree in a scientific field

Outils

GC

NMR

LIMS

TopSpin

Description du poste

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:

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.