.CSV Life Science Group, an international engineering company and a market leader in the pharmaceutical industry, is looking for a Validation Coordinator to join its team.
The resource will be hired on a full-time, permanent contract. The salary level will be proportional to experience.
REQUIRED ACTIVITY
We are looking for a validation staff coordinator. Activities include interfaces with customers and suppliers, meetings, and coordination with multidisciplinary project team.
MAIN DUTIES :
o VMP, VP, URS, GMP draft/review
FAT/SAT/Commissioning activities Supervision
Qualification protocols draft/review
Qualification protocols execution
Risk assessment writing
CANDIDATE PROFILE:
o B driving license, own car
Fluency in English
Availability for short trips
Diploma or degree in scientific subjects (CTF, chemistry, engineering)
Experience in pharmaceutical equipment/plant validation activities.
2 to 5 years of experience in manufacturing or consulting company .
Work location
Milan
We offer :
o Full-time permanent employment and career path to the best levels in the market.
Career prospects and international opportunities in multidisciplinary teams.
Pleasant and dynamic work environment.
Welfare package and company benefits.
Smart working
Our work culture
In CSV Life Science Group, you will have the opportunity to work on some of the most exciting projects in today’s market for major players in the pharmaceutical industry.
Embark on a dynamic career at CSV Life Science Group, where challenging projects and evolving customer demands keep you engaged and inspired.
On every project you work on, we offer unique experiences and exhilarating opportunities.
Create a lasting career path within a thriving international organization that values your growth and success.
