Senior Sterility Quality – Pharmaceutical Industry
Are you the right applicant for this opportunity Find out by reading through the role overview below.Walloon Brabant, BelgiumIntroductionNalys 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 leadingpharmaceutical environments.ResponsibilitiesAs a Sterility Quality Manager, you will:Act as a subject matter expert for sterility assurance within a pharmaceutical manufacturing environmentDefine, implement, and continuously improve sterility and contamination control strategiesAssess sterility risks, analyze trends, and drive preventive and corrective actionsEnsure compliance with GMP, quality systems, and regulatory expectations related to sterile productionSupport operations by providing quality input on processes, facilities, investigations, and changesContribute to inspections, audits, and internal governance related to sterility assurancePromote best practices and continuous improvement across quality and manufacturing teams.Your ProfileTo succeed in this role, you bring:A Master's degree in Engineering, Life Sciences, or equivalent scientific backgroundA significant experience in sterility assurance, quality engineering, or microbiological risk management within pharma or biotechA solid knowledge of GMP requirements and sterile manufacturing principlesExperience with risk assessments, investigations, and quality systemsStrong analytical skills and a pragmatic, solution‐oriented mindsetAbility to collaborate effectively with multidisciplinary teamsAnd you are fluent in both English and French.What We Offer / Why NalysA human‐scaled consulting company focused on expertise, partnership, and career developmentLong‐term assignments with leading pharmaceutical playersContinuous learning through technical coaching, training, and knowledge sharingA supportive culture that values autonomy, trust, and impactAn attractive salary package with additional benefits.Recruitment ProcessWhen applying for this position at Nalys, you can expect a clear and engaging recruitment journey:Talent Acquisition CallA first discussion with our Talent Acquisition Specialist, Olivia Braszko, to understand your background, motivations, and career goalsTechnical InterviewA meeting with one of our Technical Referent to evaluate your expertise and fit for the missionBusiness InterviewA conversation with the Business Unit Director, Jimmy Rousseaux, to discuss the project context and your future within Nalys.How to ApplyInterested in contributing your sterility expertise to high‐value pharmaceutical projects? xjsrcvqApply directly via LinkedIn or contact the Nalys recruitment team to start the conversation.