Jobs at Evonik

Leads facility, design, and process engineering teams within a pharmaceutical CDMO. Responsibilities include engineering strategy, team development, operational excellence, asset lifecycle and maintenance planning, capital investment, equipment design, project delivery, compliance with GMP and ISPE requirements, and continuous improvement of engineering systems and documentation.

Leads quality control planning and operations for pharmaceutical CDMO projects. Responsibilities include resource scheduling, sample management, stability testing, specification and sampling plan development, reference standard management, QC data review, client communication, and regulatory compliance. The role drives operational improvements and coordinates cross-functional QC activities in a regulated parenteral pharmaceutical environment.