Deviation Writer
Contracting – Brabant Wallon
Your Responsibilities:
· Manage the full lifecycle of deviation investigations in a GMP-regulated pharmaceutical environment.
· In the morning, assign tasks and review new deviations, conduct on-site investigations, and complete required training.
· In the afternoon, update teams on investigation progress, set resolution deadlines, and coordinate with QC and suppliers based on deviation type.
· Ensure accurate documentation and compliance with quality standards throughout the deviation process.
· Collaborate cross-functionally with internal teams and external partners to identify root causes and implement effective corrective and preventive actions (CAPA).
· Maintain high standards of communication to keep all stakeholders informed and aligned.
Your Profile:
· Proven experience in deviation management within the pharmaceutical industry.
· Strong knowledge of investigation tools, root cause analysis, and GMP compliance.
· Ability to manage deviation cases from initiation to closure with autonomy and precision.
· Clear, concise communicator with a collaborative and problem-solving mindset.
· Fluent in French and English (written and spoken).
· Comfortable working primarily on-site, with the possibility of one day of homeworking per week.
· Leadership abilities and stakeholder engagement experience are a strong advantage.
Our offer:
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, [email protected]
