Senior Computer Systems Validation Specialist (m/f)

REFERENZNUMMER:

347792/11

IHRE AUFGABEN:

-Lead a project stream for validation with the objective to set up the CSV of a MES Program (initial Core validation + rollouts)
-Ensure the completion of CSV deliverables in time and in quality
-Ensure the alignment of the different stakeholders
-Collaborate with and gives regular updates to the Project Manager
-Author, review and consult on validation documentation including but not limited to Test Scripts, Validation Plans, Installation Qualifications, SATs, UATs and Validation Reports
-Ensure compliance with corporate and global standards
-Escalate non-compliance against quality standards to appropriate governance bodies and Risk Management function for resolution
-Provide advice, expertise and train others in the requirements for Quality Assurance and provides input to Informatics process improvement projects and other cross functional programs

IHRE QUALIFIKATIONEN:

-Very good understanding of CSV in a pharmaceutical MES
-Strong project management skills and delivery focused
-Experience in validation for MES projects
-Ability to arbitrate between a wide range of stakeholders to come to a solution (former work experience with stakeholders would be a big plus)
-Strong leadership skills (former work experience as a lead would be a big plus)
-Flexible for business travels (up to 20%)
-Experience in CSV for a global program
-Understanding of the MES process
-German speaking would be a plus

WEITERE QUALIFIKATIONEN:

Business analyst