Beschreibung
For a project in Solothurn we are looking for a Project Manager
As a Project Manager within the Medical Device industry, the consultant will be providing guidance, project management and reporting activities related to Manufacturing Procedures revision activities. The resource should be versed in the writing and training of procedures describing manufacturing process with requirement from quality systems and regulation as defined by ISO and FDA.
Required skills:
5+ years. of experience within the Medical Device as a Project Manager Solid Project Management experience Knowledge of Manufacturing Procedures Good knowhow of Quality Systems (ISO 13485, FDA 21CFR 820, GMP) A working knowledge of ISO 14971 Risk and Risanagement is a plus Knowledge in MS Project is desired Background in Quality Systems is required, as the procedures to revise are related directly to the quality of the product or the quality system of the manufacturing Some ERP Knowledge (preferably Agile, JD Edwards and SAP) The person must be analytical, thorough, accurate and proficient in the use of computers in terms of Microsoft Office inclusive Visio Must be proficient in the related ISO 13485 standards sections and related 21 CFR 820 regulatory subchapters Good skills in both German and English in speaking, reading and writing are essential Strong communication skills Works effectively with cross-functional teams Proven experience in implementing Project Management Methodology within an organization Strong attention to detail Are you interested in this position? We are looking forward to receive your application. Many thanks.
