GMP Engineer
Workplace: Stockholm, Sweden
Expires: October 12, 2025
At Cellcolabs, a biotech impact scale-up specializing in large-scale production of Mesenchymal Stem Cells (MSCs), we are seeking a hands-on GMP Engineer to support clinical research by scaling production and advancing cell therapy to patients. This full-time position is based in Stockholm and involves working in a GMP-grade cleanroom environment to manufacture stem cell therapy products following strict quality standards.
Main requirements:
- Master or Bachelor degree in biotechnology, chemical engineering, molecular/cell biology, or related field
- Experience in aseptic cell culture work
- Previous experience working under strict quality requirements and GMP
- Proficiency in English
Responsibilities:
- Manufacture stem cell therapy products according to GMP in a Grade B cleanroom environment
- Plan and perform daily production tasks including stem-cell culture, routine preparations, and related documentation
- Manage documents, handle deviations, CAPA, change control, and update working instructions
- Conduct qualification and validation work per GMP framework
- Perform environmental monitoring sampling of production premises
- Manage storage and materials
- Evaluate results and raw data
- Maintain laboratory equipment and instruments and assist service technicians
Required hard skills:
- Aseptic cell culture handling
- GMP compliance and documentation
- Environmental monitoring and qualification/validation procedures
- Data evaluation related to production
- Laboratory equipment maintenance
Recommended hard skills:
- Experience working in Grade B cleanroom environment
Soft skills:
- High quality awareness
- Structured and detail-oriented
- Reliable
- Strong communication
- Team collaboration
- Proactive mindset
- Adaptability to change
Natural languages:
- English (Proficient)
Cultural skills:
- Ability to actively contribute to a positive team culture
- Supportive of colleagues
- Initiative to improve workflows and solve challenges
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