Senior Qualification Specialist
vor 1 Tag
As a seasoned professional in integrated project management, you will be responsible for designing and implementing process plants and systems worldwide that contribute to the quality of our daily lives and sustainable resource conservation.
Our core competencies cover the multifaceted requirements of our customers in the pharmaceutical, environmental, and nutrition market segments. Based on expert project management, we meet the demands of planning, process engineering, automation, assembly, qualification, and service.
International Opportunities
- We collaborate with international teams on exciting global projects.
- We take collective responsibility and value a positive working atmosphere and comprehensive social benefits.
- We provide opportunities for growth and development into experts or managers.
- We are easily accessible by public transportation and cycling paths.
Your Key Responsibilities
- You will create and verify qualification documents (DQ/FAT/IQ/OQ test plans and reports).
- You will plan and execute plant qualifications on site at our customers' premises (FAT/IQ/OQ).
- You will be responsible for coordinating qualification activities with the customer as well as the process engineering, project management, automation, and assembly departments.
- You will be familiar with the SOPs and technical standards of our clients.
- You will play a significant role in preparing GMP risk analyses.
- You will serve as deputy to the team leader.
Your Profile
- You have extensive knowledge of regulations for pharmaceutical plant engineering ((c)GMP, GEP, GAMP, etc.)
- You are fluent in written and spoken English.
- You possess a responsible, structured, and assertive personality.
- You appreciate international business trips and are flexible regarding time commitments (up to 50% travel, including internationally).
The estimated annual gross salary is approximately €55,000. The actual salary may be higher, and it will be agreed upon individually based on qualifications.
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