Responsible to perform product, process and documentation audits to determine the extent of compliance and effectiveness of operations to documented policies, procedures, specifications and regulatory requirements.
Prepares required inspection reports, defect reports and other related inspection duties in accordance with GMP’s regulations and International Standards.
Administers manufacturing course / certification in the applicable LMS System. Maintains accurate training records including course versioning offerings, attach content, version courses, manager wait lists, assisting with data cleanup.
Supports and administers on-the-job training plan to assure personnel compliance. Works with document changes in the applicable system (Ex .
change documents in Agile). Supports special projects and investigations. Support CAPA / NC reports.Contract position-Intermediate level18606-3
Requisitos - RequirementsAssociate Degree or 60 undergraduate approved credits as equivalent.3+ years of manufacturing experience with Diploma / Degree 0-
1 years of experience with Advanced Diploma or DegreeComputer LiterateBasic oral and written communication skills in Spanish and English.
Manufacturing experience in medical device, pharmaceutical, or electronic industryGood problem solving, teamwork and communication skills.
Good mathematics skillsAvailable for multiple shifts. Powered by