Minimum 7 years of Quality Assurance experience in a regulated GxP environment (GCP, GMP, GLP) within pharmaceutical or biotechnology development., Eligibility to act as a Qualified Person (QP) will be considered an additional advantage., Strong, hands-on experience relevant to the role of a QA Manager, including day-to-day QA support, cross-functional collaboration, and ownership of quality processes., Excellent understanding of Quality Management Systems and regulatory compliance frameworks., Solid knowledge of drug substance and parenteral drug product manufacturing is a strong advantage., Ability to collaborate across functional lines and work effectively in matrix environment, Strong organizational and analytical skills, with the ability to work independently as well as collaboratively., Proficiency in standard office tools (Excel, PowerPoint, Word, Outlook, Visio, etc.), Fluent English, both written and spoken, with strong communication and presentation skills., Excellent verbal and written communication and presentation skills.

sharing the costs of sports activities, private medical care, sharing the costs of professional training & courses, fruits, integration events, dental care, coffee / tea, drinks, holiday funds