Job Description The incumbent provides support for Supplier Quality Management activities of device components, active pharmaceutical ingredients (API), excipients, chemical raw materials, components, and packaging materials to proactively assure the quality and conformity of supplied materials. Coordinate completion of Specification Agreements with suppliers. Coordinate completion of Quality Agreements with suppliers. Perform assessments and actions associated with Change Control documents and Corrective/Preventive Acton's (CPA); including ownership of these records. Provide updates to Supplier Records on behalf of account owners. Support supplier investigations. Complete Supplier data for metrics and risk management documents. Support Supplier Quality projects as needed. Establish information for supplier updates in SAP. Support documentation activities for delisting of suppliers. Perform assessments for leveraging of existing audits. Assist in audit preparation of supplier audits. Other Supplier Quality departmental needs. Requirements Bachelor Degree in Sciences. 1-3 years of experience in Quality ( Documentation Specialist, Quality Assurance, QA Specialist ). Supplier Quality experience preferred. Candidate will be working remote for the Supplier Quality Americas team. cGMP (Current Good Manufacturing Practices) knowledge and experience. Computer skills – database entry, MS Office applications (Word/Excel), general electronic application use. Self-motivated. Works both individually and in a team. Effective communication; capable of coordinating with suppliers and internal departments. Full-time: 40 hours per week. Requirements Bachelor in Science: Microbiology, Biology with 4 years of experience Bilingual (Spanish/English) Technical writing