Biotechnologe (m/w/d)
Core
Plan, coordinate, and oversee method validation and verification for HPLC analytics in a GMP-regulated environment.
Role type
Scientist (Quality Control Chemistry)
Builds
Therapeutic proteins, plasmid-DNA, mRNA, viral vectors, and genetically modified cells
Domain
Biopharmaceutical CDMO
Required skills
HPLC analytics, protein analytics, method validation, GMP compliance, project management, quality management systems (TrackWise)
Preferred skills
Capillary electrophoresis, A280, Chromeleon, MS Office
Responsibilities
Planning and coordination of method validations and verifications, QC project coordination, handling deviations/CAPAs/change requests, reviewing analysis results and GMP documents, supporting internal/external audits, supporting lab investigations and method execution, coordinating with production/development/assurance teams
Seniority
Mid-level, hands-on IC
