Contracting – Brabant WallonThe company is seeking a Solutions Quality Lead to join the R&D Quality department, focusing on Good Laboratory Practice (GLP) compliance. The role is critical for supporting audit management, inspection readiness, and process improvement in pharmaceutical development. Manage and deliver GLP, GCP Lab, Toxicology, and Pharmacokinetics audits. Assign and ensure completion of audits supporting candidate development. Conduct or peer-review study plans, amendments, and reports. Contribute to process improvement by reviewing global regulations and updating SOPs and policies. Investigate non-compliance issues and facilitate stakeholder discussions for action plans. Support inspection readiness and participate in inspections by authorities or business partners. Archive audit documentation and follow up on CAPA actions. Represent R&D and PV Quality at meetings and provide guidance to team members when requested. Minimum 3 years of experience required, ideally 5 years. Experience must be in pharma, specifically GLP auditing in small molecules. Strong English language skills and French. Ability to work autonomously and transparently, with strong communication skills. Energy and motivation to raise issues and drive results. Excellent planning, organizational, presentation, training, communication, and interpersonal skills. Experience in influencing and collaborating within a global matrix organization. Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You're interested in this job? We kindly invite you to apply or send me your CV, lena.palmeri@jeffersonwells.be Support Audit, Audit, Documentation, Communication, Business, Audit, Provided Guidance, Global Regulatory, Matrix Management, Inspection, Development, Training, Process Development, GLP, Policy, Planning, Self motivated, Audit Completion, Result Oriented, Organization Skills, VOS, Quality Department, Pharmacokinetics, R&D, Archive, Audit management, Toxicology, Energy, CAPA, Audit, Updates