We specialize in undertaking projects across the nation for prominent customers in the pharmaceutical, biotechnology, and chemical industries.
To further enhance our Consulting & Solutions Division, we are seeking professionals with expertise in process automation as C&Q Engineers.
* Immediate start-up is preferred
* Location: Rhine-Main region
* Full-time work schedule
Job Position
Key Responsibilities:
* A thorough understanding of automation, commissioning, qualification, or operations within a cGMP environment
* Experience with one or more of the following industry-recognized systems: MES, Programmable Logic Controllers (PLC)
* Generating and executing validation protocols
* Application of CSV principles, concepts, practices, and standards
* Troubleshooting issues, tracking them, and building resolution plans
Essential Qualifications:
* Degree in mechanical, chemical, pharmaceutical, or general engineering
* Minimum 5 years of experience in commissioning and qualifying equipment, facilities, and utilities within the pharmaceutical sector
* Proven leadership skills to manage/coordinate
* In-depth knowledge of cGMP, CSV, GAMP5
* Fluency in business German and English; French is an asset