IPQA Supervisor, 2nd shift

Job ID 18-00159

Industry Pharma

Job Type Permanent

Location Dayton, NJ


Supervisor is to monitor all IPQA activities for all shifts if needed. Manage the scheduling for all IPQA.
Manage the syllabuses and training for all of IPQA. Help support the manager with all deviations, incidents, CAPA's, change controls for the IPQA and manufacturing floor. Be the backup and support batch record review and release activities when needed.
IPQA shall report to QA Manager. All of IPQA employees report to the supervisors.
75% Daily • Assist IPQA in all activities when needed
• Monitor IPQA and Manufacturing activities on the floor.
• Make decisions on quality and compliance issues.
• Follow up on action plans.
• Guide IPQA and Manufacturing on quality issues
• Train IPQA to improve their skills on specific activities.
• Investigate and close Deviations, CAPAs and Change Control as needed in a timely manner.
5% Daily Review analytical data used for release of raw material and finished product. Approve certificates of analysis for raw material and finished product as needed.
5% Monthly Revise applicable SOP. Train IPQA and others as applicable.
5% Monthly Prepare syllabuses verify IPQA training and perform more training if required.
10% Weekly Verify and transfer all APR data.


Perform any duties as assigned.
Monitor and trend the times it takes for IPQA room clearance and minimize this delay for all areas.
Manage the spot cleaning program for QA


Preferably a 4 year degree in a scientific discipline.
Proficient in Microsoft Office.
1-3 years of experience of manufacturing and packaging in a pharmaceutical manufacturing environment.
Minimum of 1 year of Supervisory experience in Quality Assurance/ quality Operations
Read, write and speak English