Explore 5 Jobs at Evonik Industries
Open Positions at Evonik Industries
Posted a day ago
The Assistant Project Responsible provides technical leadership and coordination for capital projects, overseeing engineering deliverables, procurement, construction support, and project documentation. The role also supports commissioning, qualification, validation, operational readiness, vendor performance, and project handover while ensuring compliance with GMP, quality, and corporate requirements.
Key Details
Top Skills Required
Posted 19 days ago
The Contract Operator performs routine equipment operations and operational tasks according to established processes and detailed instructions. The role also assists with equipment installation, maintenance, and repair, supports quality standards, and follows safety and environmental requirements.
Key Details
Top Skills Required
Top Benefits
Posted a month ago
The Associate Director of Engineering will provide strategic and operational leadership for facility, design, and process engineering teams at Evonik’s pharmaceutical CDMO site. Responsibilities include leading capital projects, asset lifecycle and reliability programs, operational excellence, compliance with GMP and engineering practices, and contributing to site strategy and team development.
Key Details
- full time Jobs
- $120,900 - $161,200 per year
- 10+ years experience
Top Skills Required
Top Benefits
Posted a month ago
The QC Specialist supports quality control operations at a pharmaceutical CDMO, coordinating QC planning, schedules, resource allocation, and project updates with internal and external stakeholders. Responsibilities include overseeing sample management and testing, preparing specifications and stability protocols, reviewing QC data, and managing reference standards to support compliant, timely delivery.
Key Details
- full time Jobs
- $77,900 - $103,800 per year
- 5+ years experience
Top Skills Required
Top Benefits
Posted 4 months ago
The Senior Project Manager, Quality Assurance oversees QA compliance and quality systems for pharmaceutical and biopharmaceutical manufacturing, including batch disposition, investigations, change controls, audits, and validation activities. The role also provides technical guidance and mentoring to QA colleagues, supports customer and regulatory audits, and drives quality improvement and reporting.
Key Details
- full time Jobs
- $101,500 - $135,300 per year
- 10+ years experience
Top Skills Required
Top Benefits
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