Project Manager Pharma / GMP

AGRAVIS is more than boots & stables. LIVISTO is an internationally operating corporate group in the field of animal health. In addition to veterinary pharmaceutical products, the product portfolio includes supplementary feed and care products for farm, pet and hobby animals as well as horses. From product development to approval, from in-house manufacturing and testing of preparations to marketing, we cover the entire entrepreneurial spectrum. In cooperation with our international subsidiaries in 11 countries, we supply our customers worldwide with our products with over 500 employees. For our subsidiary aniMedica GmbH, we are looking for a Project Manager Pharma / GMP (m/f/d) as part of a succession at the Senden Bösensell (NRW) location as soon as possible. aniMedica Herstellungs GmbH Senden-Bösensell Full-time 40.00 hours/week

• Independent management of product and technology transfers between production sites, contract manufacturers and internal departments.
• Control of transfer activities, in particular process transfer, scale-up, validation, method and document transfer as well as stability requirements.
• Planning and support of smaller construction, conversion and optimization projects for production areas, laboratories, technical systems and media supply in a GMP environment.
• Coordination of user requirements, URS, risk analyses, change controls as well as qualification and validation activities.
• Leadership of cross-functional project teams from production, quality, engineering, validation, regulatory affairs, R&D, supply chain, purchasing and controlling.
• Control of project scope, milestones, budget, resources and risks as well as regular reporting to clients and management.
• Coordination of external service providers, engineering partners, plant suppliers and contract manufacturers; support during audits and inspections.

• Completed degree in pharmacy, chemistry, biotechnology, process engineering, engineering or comparable qualification.
• Several years of project management experience in the pharmaceutical, biotechnological or comparably regulated industry.
• Proven experience with product or technology transfers in a GMP environment.
• Good knowledge of GMP, change control, risk management, qualification and validation.
• Technical understanding of pharmaceutical production facilities and building infrastructure.
• Very good German and English skills as well as willingness to travel for site-related purposes.