DescripciónDescription
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 and Quality Agreements with suppliers.
Perform assessments and actions associated with Change Control documents and Corrective/Preventive Acton’s (CAPA); 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.
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Requisitos 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.
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Requiere Mucha Experiencia
Requires Expert
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Empleos en Puerto RicoJobs in Puerto Rico
QRC GROUP LLC
Empleos en Puerto RicoJobs in Puerto RicoProfesionales
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