Your new company
A global pharmaceutical group is looking for a Quality Assurance Manager – Systems position.
Your new role
This professional will be responsible for maintaining and developing the Global Quality System, ensuring full alignment with GxP guidelines and the company’s business model. Key responsibilities include managing the Global Document System (both paper-based and electronic), implementing and monitoring Change Control processes, overseeing supplier and customer qualification, and supporting audit planning and execution. The role also involves conducting audits worldwide in accordance with GMP, GDP, GLP and ISO standards, as well as managing the Quality training system to ensure compliance with identified needs and regulatory requirements.
What you'll need to succeed
Minimum 2 years of experience in Quality Assurance area within the pharmaceutical sector, with strong knowledge of GxP guidelines and international regulatory frameworks. Experience in supplier qualification, change control processes and document management systems is essential. Strong analytical skills, attention to detail, autonomy and the ability to work with global stakeholders will be key. Fluency in English is mandatory.
What you'll get in return
Excellent opportunity to join a global role with impact, integrated in a company that values rigor, innovation and professional development.
What you need to know
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
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