Coordinate analytical studies; design protocols, planning, data analysis, reports.
Develop and implement novel QC technologies and methods.
Ensure assays meet regulatory and QMS requirements.
Qualify QC assays; support transfer/validation activities.
Document data in ELN; author SOPs and study reports.
Hybrid role: report to office 3 days/week.

🎯 Requirements

PhD in Biological Sciences + 1 year experience; or Master’s + 4 years.
Biotech experience, esp. cell therapy and pluripotent stem cells.
Extensive experience with imaging, cell-based assays, qPCR, ddPCR, RNAseq.
Good Documentation Practices and cGMP environment.
Qualification, validation, transfer, and lifecycle mgmt of analytical methods.
Technical/regulatory writing; clear data presentation.

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