Specialist Quality Assurance
FITS LLC, Juncos, Juncos, United States
For QA Services in the Downstream Area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor's Degree with five (5) years of experience within the pharmaceutical or regulated industry.
Bilingual (English & Spanish).
Project Management skills.
Shift: Administrative, and according to business needs.
Experience in:
Quality Systems, including Deviations (Nonconformities), CAPA, and Change Control.
Documentation platforms (e.g., CDOCS), Maximo, TrackWise, LIMS, MES/electronic batch record systems, and SAP.
Computer systems validation (CSV) or computer systems quality assurance.
Validation of GxP applications, including Validation Master Plans, GxP risk assessments, and IQ/OQ/PQ protocols.
The Personality Part:
Picture yourself in a lab... with all the equipment you need to put your multitasking, scientific, creative (to come up with all those experiments!) skills to work. Picture as well an environment of healthy competition, teamwork, being ethical, and of using the scientific method in all ways possible. If you like how this sounds, then this might be the job for you. Bring it on!
AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)
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.
Provide lot disposition and authorize lots for shipment.
#J-18808-Ljbffr
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor's Degree with five (5) years of experience within the pharmaceutical or regulated industry.
Bilingual (English & Spanish).
Project Management skills.
Shift: Administrative, and according to business needs.
Experience in:
Quality Systems, including Deviations (Nonconformities), CAPA, and Change Control.
Documentation platforms (e.g., CDOCS), Maximo, TrackWise, LIMS, MES/electronic batch record systems, and SAP.
Computer systems validation (CSV) or computer systems quality assurance.
Validation of GxP applications, including Validation Master Plans, GxP risk assessments, and IQ/OQ/PQ protocols.
The Personality Part:
Picture yourself in a lab... with all the equipment you need to put your multitasking, scientific, creative (to come up with all those experiments!) skills to work. Picture as well an environment of healthy competition, teamwork, being ethical, and of using the scientific method in all ways possible. If you like how this sounds, then this might be the job for you. Bring it on!
AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)
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.
Provide lot disposition and authorize lots for shipment.
#J-18808-Ljbffr