GMP Validation Engineer – Pharmaceutical Equipment

Aenova Group, at the Borgo San Michele LT site in Italy, is looking for an Engineering Validation Specialist to contribute to qualification activities for manufacturing equipment, process systems, utilities and laboratory instruments. You will prepare GMP documentation (URS, DQ, IQ, OQ, PQ) and support FAT/SAT, collaborating with Engineering, Production,...

Aenova Group, at the Borgo San Michele LT site in Italy, is looking for an Engineering Validation Specialist to contribute to qualification activities for manufacturing equipment, process systems, utilities and laboratory instruments. You will prepare GMP documentation (URS, DQ, IQ, OQ, PQ) and support FAT/SAT, collaborating with Engineering, Production,...

Haupt Pharma Latina S.r.l., a member of the Aenova Group, is seeking an Engineering Validation Specialist for its site Borgo San Michele LT, Italy. You will plan, execute, and maintain GMP qualification activities for equipment and utilities used in pharmaceutical manufacturing.Ideal candidates have 2–3 years in qualification/validation in pharma or...

Haupt Pharma Latina S.r.l., a member of the Aenova Group, is seeking an Engineering Validation Specialist for its site Borgo San Michele LT, Italy. You will plan, execute, and maintain GMP qualification activities for equipment and utilities used in pharmaceutical manufacturing.Ideal candidates have 2–3 years in qualification/validation in pharma or...

Haupt Pharma Latina S.r.l., a member of the Aenova Group, is seeking an Engineering Validation Specialist for its site Borgo San Michele LT, Italy. You will plan, execute, and maintain GMP qualification activities for equipment and utilities used in pharmaceutical manufacturing.Ideal candidates have 2–3 years in qualification/validation in pharma or...

CAI Overview Are You Ready? CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For Life Sciences and Mission Critical industries that need to deliver critical solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled performance at the highest...

Fortil, gruppo internazionale nel settore ingegneria e tecnologia, cerca un Equipment and System Validation Engineer da inserire nel team Engineering & Quality per garantire qualifica e convalida di apparecchiature, impianti e sistemi per produzione farmaceutica, con focus su ambienti sterili e processi asettici. La risorsa supporterà la conformità GMP, la...

S.T.B. ValiTech S.r.l., società di consulenza specializzata nel settore Life Science, ricerca Validation & Qualification Engineer da inserire in progetti GMP in ambito farmaceutico, chimico e biotech. La risorsa sarà coinvolta in attività di commissioning, qualification e convalida di impianti, equipment di processo, clean utilities e sistemi di...

for the site Borgo San Michele LT, Italy Your key responsibilities The Engineering Validation Specialist is responsible for planning, executing, documenting, and maintaining qualification activities for GMP equipment and utilities used in pharmaceutical manufacturing environments in compliance with applicable regulations (laws, GMP, FDA, etc.), the...