Vacancy Description
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.
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