About us
Introduction
Nalys is a Belgian recruitment and consultancy firm specialised in the pharmaceutical, biotech and life sciences industries. With deep expertise across quality, regulatory affairs, manufacturing, engineering and clinical development, we support both large international groups and innovative scale-ups in building the teams that drive their projects forward. When we place a professional, we stay by their side — before, during and after the mission.
Today, we're looking for an experienced Compliance Support Specialist to join a QA Operations team within a sterile injectable manufacturing environment in the Brabant wallon area. This is a full replacement role — you'll be fully operational from day one, owning deviation management end-to-end in a demanding, high-standard GMP setting.
Job Description
Your Responsibilities
As the future new Compliance Specialist, you will:
Own the full deviation management cycle in a Fill & Finish sterile manufacturing environment — from initial detection through to closure
Conduct product and process impact analyses with a structured, scientific approach
Lead root cause investigations, including on-the-floor Gemba walks in production areas
Write and document deviations with precision, clarity and full GMP compliance
Review batch records directly in production zones
Coordinate investigations with Production, QA and Microbiology teams
Provide supporting input during audits and regulatory inspections.
Required qualifications
Your Profile
You hold a Master's degree in biology, chemistry, biochemistry, engineering or a related scientific field — or a Bachelor's degree with strong compensating experience
You have minimum 2 years of hands-on experience in a GMP pharmaceutical environment
A direct experience in Fill & Finish or injectable manufacturing is strongly preferred
You need a proven track record in deviation management — you write, investigate and close deviations independently
You are fluent in french
And analytical, structured and solution-oriented mindset
You feel comfortable with on-site presence in controlled production areas, including gowning requirements and removal of jewelry and piercings
Experience with SAP, LIMS, deviation management tools or electronic batch record systems (OP Center) is a genuine asset.
What's on 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
An attractive salary package with additional benefits.
Our recruitment process
When applying for this position at Nalys, you can expect a clear and engaging recruitment journey:
Talent Acquisition Call
A first discussion with our Talent Acquisition Specialist, Olivia Braszko, to understand your background, motivations, and career goals
Technical Interview
A meeting with one of our Technical Referent to evaluate your expertise and fit for the mission
Business Interview
A conversation with the Business Unit Director, Jimmy Rousseaux, to discuss the project context and your future within Nalys.
Interested?
This role is for you if you thrive on turning quality challenges into lasting solutions.
👉 Send your application directly here — we look forward to connecting with you.
