1 year contract hybrid Job Model French speaking desired
Are you passionate about bridging IT and Quality in a highly regulated environment We are looking for an experienced Life Science professional to take on a pivotal role ensuring IT compliance and quality oversight across complex manufacturing systems.
What youll do
- Act as the key contact between IT and Quality fostering a strong quality culture.
- Ensure compliance of site IT systems with GxP EU-GMP Annex 11 and 21 CFR Part 11.
- Lead Computer System Validation (CSV) activities and support data integrity programs.
- Translate compliance requirements into test strategies (FAT SAT IQ OQ PQ).
- Partner with cross-functional teams and external stakeholders to drive compliance and continuous improvement.
- Support audits infrastructure integration and remediation projects.
What you bring
A degree in Life Sciences Quality Engineering or related field.510 years of experience in the pharmaceutical biotech or life science industry with at least 5 years in IT compliance validation or quality roles.Solid knowledge of Quality Management Systems GxP systems (MES LIMS etc.) and Data Integrity.Strong IT foundation (OS infrastructure networking systems).Expertise in CSV and regulatory frameworks (21 CFR Part 11 EudraLex MHRA).Excellent communication skills a structured and analytical mindset and the ability to thrive in an international multidisciplinary environment.Why join
This is a unique opportunity to contribute to high-impact manufacturing operations ensuring compliance data integrity and patient safety. Youll work in a dynamic environment that values ethics collaboration and continuous learning.
Key Skills
Quality Assurance,FDA Regulations,Food Industry,Food Safety Experience,ISO 9001,Quality Systems,Food Processing,Quality Control,Quality Management,QA / QC,Selenium,HACCP
Employment Type : Full Time
Experience : years
Vacancy : 1