Senior Associate Quality Control
Target PR Range: 30-40/hr
*Depending on experience
• Working collaboratively with Quality and Quality Assurance teams to author and own change control records and deviations in the DQMS Veeva System
• Individual will lead investigation teams and help to collect and report metrics for the systems team
• Individual may assist with review of validation documents to support equipment and computerized system onboarding.
• Individual may author, revise and review documents and reports including but not limited to SOPs, test methods, safety assessments, trend reports, qualification/validation summary reports, technical reports.
• Support the startup of a GMP QC laboratory.
• Support routine activities over the weekends and public holidays as required.
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