Day to day activities to support VEROPHARM Quality Management System (QMS) and VEROPHARM level QMS Documentation.
Provide support to Quality Managers at manufacturing sites in managing site Quality Systems.
Provide QA support and guidance regarding training, metrics and management review ensuring compliance with regulations and Abbott & VEROPHARM Quality System requirements.
Manage Change Control and Corrective and Preventative Action (CAPA) processes at VEROPHARM level.
Create and maintain data, documentation and systems to track, monitor, and support quality metrics and management review program.
Support for the Training Quality System, create training materials and deliver training as requested, maintain training plans for assigned staff.
Support projects and programs as assigned by Management (e.g. review of documents, records, reports, survey results, document control – upload and retrieval and routing for approval through electronic documentation management system etc.).
Participate in QA cross-functional teams to support the region.
Participate in QA audits of manufacturing sites.
Provide support in maintaining a program/project management process to support quality and compliance initiatives in the region and at the sites.
Bachelor’s Degree or equivalent in life science.
At least 3 years of experience in QA Function in Pharmaceutical environment.
Ability to communicate effectively, both orally and in writing for both technical and non-technical audience.
Teamwork attitude and capability of understanding and overcoming different cultural and language obstacles to provide solutions satisfying corporate, divisional and local objectives.
Ability to use Quality Risk Assessment and Root Cause Analysis tools.
English language knowledge at least at Intermediate level.
Work with a highly professional team
Good benefit package
Opportunity of professional and career growth
Medical and life insurance