Argenx is a clinical-stage biopharmaceutical company that is creating and developing a pipeline of differentiated antibody therapeutics. Our unique antibody engineering technologies combined with the complementary expertise of our people enabled us to build a clinical-stage portfolio of novel product candidates – tailored from discovery through development to address patient needs.
For the expansion of our BIS team, argenx is looking for a (Senior) IT Quality & Validation Manager
The (Senior) IT Quality & Validation Manager is responsible for the day to day operations and coordination of all activities relating to the argenx Computer Systems Validation (CSV) Process. This ranges from Initial Impact Assessment, through initial implementation, managing Saas Release validation, and solution retirement.
Key Accountabilities/Responsibilities:
The position will have the following key responsibilities:
1. Monitor and ensure successful completion of Release Management of all argenx platforms/solutions.
2. Drives (together with the appropriate functions) the planning and preparation of essential documents to a quality standard:
3. Own the Computer Systems Validation SOP.
4. Partner closely with the QA function at argenx to ensure alignment with all SOPs.
5. Ensure CSV SOP is fully aligned with the latest guidance from EMA/FDA/PDMA.
6. Ensures timely, open and effective communication to relevant stakeholders
7. Teams, collaborators, management, contractual partners
8. Manages external CVS partner to get a highly engaged and motivated team.
9. Liaise with the appropriate BIS functions to perform the original CSV assessment, final implementation validation, AND define release management strategy for each platform.
10. Support all tool audits together with the Finance audit function at argenx.
11. Align GDPR, HIPAA and APPI guidelines with the Legal function at argenx.
Desired Skills and Experience:
12. Minimum of 5-7 years working either in or near a biopharmaceutical medical or development sciences function, either within BIS/IT and/or in a development sciences function.
13. Experiences as Validation lead for computer systems in a regulated industry.
14. Experience SmartSheets for project tracking.
15. Understanding of the industry landscape and global regulatory requirements (e.g. GxP, HIPAA. GDPR, APPI, etc..).
16. Excellent attention to detail and documentation.
17. Demonstrated ability to work, effectively communicate, and influence at multiple levels within multidisciplinary organization.
18. Demonstrated ability to manage external service providers and budgets.
19. Demonstrated ability to monitor many project release schedules.
20. Adeptness in anticipating potential areas of extra focus as identified during the CSIA phase.
Offer:
21. A competitive salary package with benefits;
22. A work environment in a human-sized, dynamic, rapidly growing biotech company
Apply:
Your application and related information will remain strictly confidential.