Technical quality specialist

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!