Questa posizione è in GSK
Il processo di selezione sarà interamente gestito GSK.
Questa occasione è disponibile in Ware, Siena - Italy, Worthing, Barnard Castle, Wavre - Belgium, Tres Cantos - Spain, Rixensart - Belgium, Parma - Italy.
--
Are you an experienced Biopharm, Vaccines, or Pharmaceutical professional looking for an exciting opportunity to leverage your expertise to support GSK Senior Management in the identification, prioritisation, and monitoring of quality, compliance, and technical risks? If so, this role within our Quality organisation could be a great opportunity for you. Position Details: The purpose of the Audit Senior Lead role is to perform and manage GMP (Good Manufacturing Practice) and Compliance audits of Biopharm, Vaccines, and Pharmaceutical facilities that supply highly regulated markets. You will be responsible for evaluating the compliance of GSK Global Supply Chain (internal and external) facilities with GMP, applicable policies and procedures, and regulatory and contractual commitments.
Your remit will include audits of (Global Supply chain internal and external networks) manufacturing facilities and operations, Local Operating Companies (LOCs), R&D; and Logistics Service Providers (LSPs). In this role, you will also provide sterile manufacturing subject matter expertise for the GSK Global Supply Chain EMEA auditing team. Strong communication and influencing skills will be key to success. Key Responsibilities include: More experienced staff may undertake:
- Manage complex stakeholder engagement for audits across the network (which may include Supply Chain Directors, Site Directors, Site Quality Directors, VPs/Heads of support functions, and Research & Development Quality).
Typical work output will involve:
- Performing audits of Global Supply Chain (GSC) sites, LOCs, and external manufacturing sites (including R&D;), LSPs and facilities supplying EMEA and other highly regulated markets.
- Preforming Unannounced audits.
- Preforming
📌 Audit Senior Lead (Siena)
🏢 Gsk
📍 Siena