Polpharma Biologics is a state-of-the-art biological R&D and manufacturing facility, one of the most modern in Europe. We have a fantastic, international team of experienced experts and dynamic young scientists with common goals and values. Biotechnology is our passion.
Together we develop medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!
Shaping IT Policies and Procedures for Polpharma Biologics and cooperating within the global organization to harmonize processes;
Evaluating the efficiency of IT controls and continuously improving them;
Reporting risks or non-conformity issues;
Driving an IT Audit readiness program;
Participating in IT-related Deviation, CAPA, and Change Control Management;
Developing and maintaining training plans, training matrices, and training compliance within the IT organization;
Collaborating with IT, QA, Engineering, other business units, contractors, and vendors to monitor and enforce standards and regulations.
If you have
Experience in IT in the Pharmaceutical or similarly regulated industry;
Experience in implementation and maintenance of SOPs, change management, and risk management;
Knowledge and understanding of the latest industry information security trends and lifecycle management of computerized systems;
Ability to recognize and solve problems independently, good organization and presentation skills, and the ability to work efficiently under time pressure;
Must be well-organized and a team player with excellent communication skills;
It is preferable to have higher educational qualifications in Computer Science, Engineering, or other technical related fields.