Job description

Job Description

Join our team and start a new adventure in an international and dynamic environment, where you will be able to fulfil your career expectations in a fast-growing organization. You’ll have the opportunity to work within our Life Sciences team, supporting pharmaceutical manufacturing operations and ensuring the highest standards of quality and compliance.

Your missions

• Review and approve electronic batch records in accordance with GMP requirements, internal procedures, and regulatory standards.


• Identify discrepancies, documentation errors, and data integrity issues within electronic batch records.


• Collaborate with Production, Quality Assurance, and other relevant teams to investigate and resolve batch record issues.