Global Supply Chain Quality Metrics & Documentation, Senior Associate City: **Your responsibilities** Reporting to the Supplier Quality Programme Senior Manager, the primary scope of the role: • Co-ordinates the documentation assistant activities to ensure compliance verification activities are completed as per the required timelines globally. • Ensures systems and processes are in place to ensure quality technical agreements and all other supplier compliance documents and certificates are in place and within date globally • Escalation within GSCQ where compliance verification gaps exist and establish plans to remediate, partnering closely with procurement where supplier leverage is required. • Reports KPI’s relating to documentation compliance and identifies supplier compliance risks. • Supports the creation of content for review at the Supply Chain Quality Monthly Review and Quarterly Management review meeting. • Maintains the EMO Quality Manual in line with Reckitt expectations and or regulatory requirements and ensures these are deployed to the area EMO Quality teams for deployment. • Analyses the KPI metric data for GSCQ to drive continuous quality improvement • Monitors and reports progress on Quality Improvement Initiatives • Drives improvements in performance and reporting through simplification and use of technologies. Please note that the duties and responsibilities within this role may change over the course of employment, which will require flexibility **The experience we're looking for** • Broad understanding of supplier management, EMO management and quality management systems • Strong collaboration and partnership skills. Capable of working both vertically and horizontally within the organisation • Excellent communication skills, a continuous improvement mindset and ability to facilitate change. • Excellent risk management skills to identify and mitigate supplier risks to the business. • Flexibility with working hours due to the different time zones associated with a global role. • Degree or equivalent in a relevant scientific discipline is desirable, suitable experience will be considered • Minimum of 5 years’ experience within a Health environment • Excellent understanding of supplier and EMO quality requirements • Excellent PC skills particularly Excel, Outlook, Word • Experience in a GMP environment. • Internal / External audit experience preferred **The skills for success** Key challenges • Working with and data management of 8000+ suppliers of materials globally. • Be accountable for the compliance verification activities being completed to the required timelines and reported as per the compliance verification scorecard. • Ensure relevant supplier quality documentation and databases are maintained. • Effectively prioritise workload on the basis of risk assessment and generation of business benefit. • Minimise regulatory adverse comment with regard to contractors or supply base