Senior Sterility Quality – Pharmaceutical Industry
Learn more about the general tasks related to this opportunity below, as well as required skills. Walloon Brabant, Belgium Introduction Nalys is a Belgian consulting company specialized in life sciences and high‐regulation environments. We support pharmaceutical and biotech companies by providing expert engineers and quality professionals who contribute to critical industrial and quality missions across Belgium and France. We are currently looking for a Senior Sterility Quality Engineer to join our team and support one of our pharmaceutical partners located in Walloon Brabant in Belgium. This role offers a unique opportunity to work at the heart of sterile manufacturing activities, where quality, patient safety, and regulatory excellence are key drivers. By joining Nalys, you will be part of a human‐sized organization that values expertise, long‐term partnerships, and continuous development, while working on impactful projects within leading pharmaceutical environments. Responsibilities As a Sterility Quality Manager, you will: Act as a subject matter expert for sterility assurance within a pharmaceutical manufacturing environment Define, implement, and continuously improve sterility and contamination control strategies Assess sterility risks, analyze trends, and drive preventive and corrective actions Ensure compliance with GMP, quality systems, and regulatory expectations related to sterile production Support operations by providing quality input on processes, facilities, investigations, and changes Contribute to inspections, audits, and internal governance related to sterility assurance Promote best practices and continuous improvement across quality and manufacturing teams. Your Profile To succeed in this role, you bring: A Master's degree in Engineering, Life Sciences, or equivalent scientific background A significant experience in sterility assurance, quality engineering, or microbiological risk management within pharma or biotech A solid knowledge of GMP requirements and sterile manufacturing principles Experience with risk assessments, investigations, and quality systems Strong analytical skills and a pragmatic, solution‐oriented mindset Ability to collaborate effectively with multidisciplinary teams And you are fluent in both English and French. What We Offer / Why Nalys 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. 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. How to Apply Interested in contributing your sterility expertise to high‐value pharmaceutical projects? xjsrcvq Apply directly via LinkedIn or contact the Nalys recruitment team to start the conversation.