- Scientific academic background, preferably in pharmacy, biology, chemistry or another life science.
- Sufficient experience in a regulated environment either in regulatory affairs or quality, preferable in pharmaceutical industry.
- Very good skills in English.
- Well organized person and capable of managing multiple projects at the same time
- Ability to work independently and pro-actively.
- End-to-end process management experience is advantage.

- Provide administration of E2E change management. You are responsible to drive and coordinate change requests related to GxP relevant business process and master data maintenance.
- Ensure timely implementation of all on-going life-cycle activities (change requests).
- Liaise with different stakeholders (e.g. regulatory affairs, commercial and/or supply chain department, business process owners) to facilitate working out and implementation of change requests.
- Support the realization of global and cross-functional quality improvement projects.
- Ensure GxP compliant documentation and internal procedures, processes and quality-systems are consistently applied proactively.

Acino offers learning and development opportunities, compensation package that values your work, modern working conditions, flexible working hours and possibility to combine office and remote work, team events, additional paid Acino days. Workplace situates in Põlva.

To apply please s apply via button below by 12.02.2023.