Description
- Completes on-site supplier audits for Drug and Biologics team. Requires up to 35% travel, including international locations.
- Identifies supplier compliance issues; helps to resolve issues in a timely manner.
- Partners with facilities, divisions, and regions to ensure successful implementation and compliance to CQP / regulations.
- Own and resolve supplier related CAPA(s). Analyze supplier related defect data to determine root cause.
- Partners with Global Purchasing to right size the supplier base and continuously improve supplier relationships.
- Development and implementation of procedures affecting several business groups and functions.
- Understands and assures conformance to regulations for Drug and Biologic suppliers. May interfaces with regulators during regulatory inspections.
- Participate in or manage quality assessments of internal operations and suppliers to analyze compliance and assess risk.
- Interacts frequently with subordinate supervisors and functional peer group managers.
- Identifies and manages continuous improvement projects with the objective of achieving quality, reliability and cost improvements.
- Utilizes the Global Supplier Quality Trackwise System (GSQTS) for maintaining Supplier Quality Records.
Must have requirements:
- 5 years + experience working in Quality
- Bachelors degree in Science / Engineering
- Strong supplier development experience
- Strong auditing experience
- Experience with API Manufacturing (must have)
f you have all of the above experience and you're interested in hearing more, please send me your updated resume or forward on to anyone in your network who may be interested.
To find out more about Real please visit www.realstaffing.com