CSV Life Science Group, an international engineering company and a market leader in the pharmaceutical industry, is looking for a
Validation Specialist.
The resource will be hired on a full-time, permanent contract. The salary level will be proportional to experience.

We are looking for a validation engineer. The figure will work in the validation division and will be located in Ancona. Activities include interfaces with customers and suppliers, meetings, and coordination with multidisciplinary project team.

Main duties
Coordinating the validation staff on field.
VMP, VP, URS, GMP draft/review.
FAT/STA/Commissioning activities supervision.
Qualification protocols draft/review
Qualification protocols execution
Risk assessment writing

Candidate profile
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.
Availability for short trips .
B driving license, own car .
Fluency in English.

Work location :

We offer
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.


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