CPP specialist

Job Description

Explained :

The job description is for an Ancillary Associate, whose main responsibilities include arranging and compiling legal documents, such as CPP, Mfg Lic, GMP, FSC and others, from various sources, such as health authorities and manufacturing sites, for submission purposes. The Ancillary Associate is also responsible for reviewing, printing and submitting these documents to foreign government health authorities, and coordinating with them to obtain the final ancillary documents. They also need to coordinate with manufacturing sites and vendors to arrange for notarization, apostillation, and legalization of documents in line with country-specific requirements. Other responsibilities include peer-reviewing legal documents, preparing status reports and metrics for ancillary documentation activities, archiving final documents to Veeva Vault RIM, and updating trackers and sharepoints. The ideal candidate should have a Bachelor's degree in science, engineering or related field and basic knowledge of pharmaceutical terminology, and experience with Veeva Vault / RIM is an advantage. They should also have excellent organizational skills, be able to multitask and communicate effectively with key stakeholders.

For Germany

• English basic is required-As person must communicate with the project manager who don't speak German and to review the application in English Language
• German writing / Speaking
• Find profile anywhere in Germany, and 1-2 years’ experience is also fine but check (Basic knowledge on CPP, GMP. Manufacturing License, Notarization, Legalization) priority on ask criteria.