QA & Deviations Specialist

Quality Consultant – Deviation Management

📍 Brussels Area, Belgium

About Nalys

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

About the Role

We are currently looking for a Quality Consultant to join one of our pharmaceutical partners for an on-site mission focused on deviation management within a GMP manufacturing environment. The consultant will play a key role in ensuring compliance and driving continuous improvement in quality processes.

Responsibilities

• Manage deviations from end to end: identification, root cause analysis, implementation of immediate and preventive actions, and effectiveness checks
• Handle deviations of varying criticality: minor, major, and critical
• Communicate with external stakeholders regarding deviation investigations and resolutions
• Draft clear and concise technical documentation in English
• Collaborate closely with manufacturing, quality, and engineering teams
• Support audits and inspections related to deviation handling
• Promote a proactive and solution-oriented mindset within the team.

Skills & Qualifications

• You hold a Master’s degree in Engineering, Life Sciences, Pharmacy, or related field
• You have proven experience in deviation management within the pharmaceutical industry
• You understand perfectly GMP's and quality systems
• An experience in sterile manufacturing or aseptic filling is a strong asset
• You communicate fluently both in French and English
• A Lean Six Sigma Yellow or Green Belt certification is a plus
• Strong time management and organizational skills
• Team-oriented, proactive, and able to take initiative.

Recruitment Process

1. Olivia Braszko, Talent Acquisition Specialist at Nalys, will review your application and schedule an initial screening
2. A technical interview will be conducted with our Technical Director
3. Final validation will be done with our Business Unit Director, Jimmy Rousseaux, and the client.