Senior Qualification & Validation Engineer (GMP) | Innovative Biotech Manufacturing

Náplň práce, právomoci a zodpovednosti:
- Provide technical oversight of manufacturing and utility/support equipment, including monitoring and testing activities
- Plan, execute and evaluate equipment and process qualification/validation activities (IQ/OQ/PQ)
- Review results, analyse data and prepare validation reports and related documentation
- Create and maintain GMP-compliant documentation (protocols, records, Validation Master Plan – VMP)
- Coordinate change control and manage deviations during qualification and validation activities
- Propose and implement continuous improvements of equipment and processes based on validation findings

Zamestnanecké výhody, benefity:
- Stock options – opportunity to participate in the company’s long-term value creation and growth
- Sick days
- MultiSport card
- Meal allowance of €5 per day
- A unique opportunity to contribute to the development of an innovative platform from the ground up
- Work in a small, expert team, where every employee has a real impact on the company’s direction and development outcomes

Požiadavky na zamestnanca:
- Master’s degree (MSc) in Chemical Engineering, Mechanical Engineering, Automation Engineering, Biotechnology, Natural Sciences or a related field
- 6–10 years of experience in qualification and validation within pharmaceutical, biotechnology or other regulated environments
- Solid understanding of GMP requirements and validation principles
- Proven experience in the preparation, execution and approval of qualification and validation documentation
- Independent, structured and systematic approach with strong technical problem-solving skills
- Advanced English language proficiency (C1 level)