Technical Quality Specialist (Deviation)
Walloon Brabant, Belgium
Introduction
At Nalys, we are passionate about engineering, technology, and life sciences. As a fast‑growing consultancy company, we support leading pharmaceutical organizations across Europe by providing high‑value technical expertise and a human‑centered approach.
For one of our trusted partners in the Brussels area, we are looking for a Technical Quality Specialist to strengthen technical quality activities within a GMP‑regulated environment. This role offers a great opportunity to contribute to meaningful quality processes while growing within a dynamic and supportive engineering community.
Responsibilities
As the new Technical Quality Specialist, you will have to :
Manage technical deviations from initiation to closure, ensuring timely and compliant documentation
Support CAPA and Change Control processes linked to technical, maintenance, and engineering activities
Create, review, and update quality documentation (SOPs, work instructions, forms, checklists)
Provide administrative and quality support to technical teams, including supplier requests, purchase coordination, and documentation archiving
Prepare and consolidate KPIs related to quality, safety, performance, and technical activities
Contribute to internal and external audits by ensuring accurate and compliant documentation
Collaborate with cross‑functional teams such as Quality, Production, Engineering, Maintenance, Purchasing, and HSE.
You Profile
You hold a Degree in a technical, scientific, or pharmaceutical field
You have minimum 2 years of experience in a GMP/ISO‑regulated environment (pharma, biotech, medical devices…)
You Demonstrate experience managing deviations, CAPA, and quality documentation
You act as a specialist of MS Office usage; experience with TrackWise, EDMS, SAP, or similar tools is a strong asset
You are details oriented, with an analytical mindset
You are are to manage priorities autonomously and work efficiently with different stakeholders
You are fluent in both English and French.
Why Join Nalys?
A people‑focused culture built on trust, development, and technical excellence
Personalized career development paths and regular follow‑up with our technical leaders
Access to a broad range of projects within the pharmaceutical and life sciences industry
Internal training opportunities, communities of practice, and a strong knowledge‑sharing environment.
Recruitment Process
By applying for this position, you will go through our standard Nalys recruitment journey:
First conversation – Olivia Braszko, Talent Acquisition Specialist, will review your application and schedule an initial introduction call
Second interview – Meeting with the Business Unit Director, Jimmy Rousseaux, to validate your fit with Nalys’ culture and mission.
How to Apply
Ready to grow your career in pharmaceutical quality?
Send us your CV — we’d love to meet you!