Groupe PARIMA has been active in development and contract manufacturing since 1994. Over the years, we have acquired expertise in the development of non-sterile pharmaceutical products in liquid, semi-solid or suspension form. We work closely with our customers to provide a tailor-made service that meets their needs. Whether it’s an entirely turnkey service or development … Continued
Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO), established in 1994. For over 30 years, we have developed an expertise in the development and manufacturing of non-sterile liquids, suspensions and semi-solid drug products. https://www.groupeparima.com/fr/ Process and Cleaning Validation Specialist The Process and Cleaning Validation Specialist is responsible for activities related to validating the … Continued
Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO), established in 1994. For over 30 years, we have developed an expertise in the development and manufacturing of non-sterile liquids, suspensions and semi-solid drug products. https://www.groupeparima.com/fr/ Computerized Systems Validation SpecialistResponsible for the Computer Systems Validation Master Plan. Responsabililities: • Develop and review computerized systems validation … Continued