Supplier Quality Compliance

As a candidate for this role, your key responsibilities will include: - Issue Documentation & Resolution: - Create and maintain documentation when an issue is raised. - Work directly with suppliers to ensure effective Corrective Actions and Preventive Actions (CAPA) are implemented. - Track these actions to prevent recurring issues in quality, delivery, or production. - SCAR Management: - Manage Supplier Corrective Action Requests (SCARs) with over 100 open SCARs. - Collaborate with various internal teams and suppliers to close SCARs within agreed timelines. - Root Cause Analysis & Prevention: - Determine the cause of quality issues, prevent them, and ensure supplier commitments are followed. - Investigate why corrective actions failed in case of repeat issues and escalate as needed. - Cross-Functional Coordination: - Communicate resolutions and preventive measures with internal teams. - Share supplier commitments and ensure adherence across different functions. You should preferably have a background in Biopharma or Pharma Manufacturing, but candidates from any manufacturing sector are welcome. Experience in Quality Control (QC) or Quality Assurance (QA) is relevant. Familiarity with CAPA processes, SCARs, PPM (Parts Per Million), supplier management, documentation, and company quality policies is required. In addition to the responsibilities, you should possess the following desired skills and attributes: - Global exposure is essential, with experience working with international stakeholders. - Ability to coordinate and drive resolutions across different global manufacturing sites. - Strong governance, dashboard reporting, escalation management, and process improvement skills.,