We are sourcing a contractor to perform on site services for the Quality Assurance program to review and approve product MPs, approve process validation protocols and reports for manufacturing processes, request quality on incident triage team, approve environmental characterization reports, release of sanitary utility systems, approve planned incidents, represent QA on NPI team, lead investigations, lead site audits, own site quality program procedures, designee for QA manager on local CCRB, review risk assessments, support automation activities, support facilities and environmental programs,review and approve Work Orders, review and approve EMS/BMS alarms, approve NC investigations and CAPA records, approve change controls among others.
Must have: Bachelors Degree. Bilingual (English & Spanish). Must have experience performing Investigations, Change Control and CAPA in a pharmaceutical site with 5 plus years of directly related experience. Excellent Technical Writing skills. Qualified resources please submit your resumes in MS Word format today.
Contacto - Contact
Sara P. Odeh Torres
sodeh@alpharmapr.com
Puerto Rico
