As an integrated project specialist, Bilfinger Life Science designs and builds process plants and systems worldwide contributing to improve the quality of our daily lives and sustainably conserving resources.
Our core skills cover the multifaceted requirements of our customers in the pharmaceutical, environmental and nutrition market segments. Based on professional project management, we meet the requirements of planning, process engineering, automation, assembly, qualification and service.
Our offer
* We work on exciting international projects
* We take responsibility together
* We value a first-class working atmosphere and our social benefits
* We grow and develop individually into experts or managers
* We are very easy to reach by public transport and cycle paths
Your tasks
* You create and check qualification documents (DQ/FAT/IQ/OQ test plans and reports)
* You plan and carry out plant qualifications on site at our customers (FAT/IQ/OQ)
* You are responsible for the coordination of qualification activities with the customer as well as with the process engineering, project management, automation and assembly departments
* You are familiar with the SOPs and technical standards of our customers
* You are significantly involved in the preparation of GMP risk analyses
* You are the deputy of the team leader
Your profile
* You have good knowledge of the regulations for pharmaceutical plant engineering ((c)GMP, GEP, GAMP, etc. advantageous)
* You are business fluent in written and spoken English
* You are a responsible, structured and assertive personality
* You appreciate international business trips and are flexible in terms of time (up to 50% travel, also internationally)
Collectively agreed annual gross salary starting at € 55.. The actual salary is higher and will be agreed individually depending on qualifications.